Canonical Allele Identifier: CA1139662098
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 929939
dbSNP Id: rs1954226902

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77172741_77172750delinsATCGGCTGCT , CM000673.2:g.77172741_77172750delinsATCGGCTGCT GRCh38
NC_000011.9:g.76883787_76883796delinsATCGGCTGCT , CM000673.1:g.76883787_76883796delinsATCGGCTGCT GRCh37
NC_000011.8:g.76561435_76561444delinsATCGGCTGCT NCBI36
NG_009086.1:g.49478_49487delinsATCGGCTGCT
NG_009086.2:g.49496_49505delinsATCGGCTGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.1798-7_1800delinsATCGGCTGCT
ENST00000669443.1:c.162-7_164delinsATCGGCTGCT
ENST00000409619.6:c.1765-7_1767delinsATCGGCTGCT
ENST00000409709.7:c.1798-7_1800delinsATCGGCTGCT
ENST00000409893.5:c.1798-7_1800delinsATCGGCTGCT
ENST00000458637.6:c.1798-7_1800delinsATCGGCTGCT
ENST00000620575.4:c.1798-7_1800delinsATCGGCTGCT
NM_000260.3:c.1798-7_1800delinsATCGGCTGCT
NM_001127179.2:c.1798-7_1800delinsATCGGCTGCT
NM_001127180.1:c.1798-7_1800delinsATCGGCTGCT
XM_005274012.2:c.1798-7_1800delinsATCGGCTGCT
XM_006718558.2:c.1798-7_1800delinsATCGGCTGCT
XM_006718559.2:c.1798-7_1800delinsATCGGCTGCT
XM_006718560.2:c.1798-7_1800delinsATCGGCTGCT
XM_006718561.2:c.1798-7_1800delinsATCGGCTGCT
XM_011545044.1:c.1798-7_1800delinsATCGGCTGCT
XM_011545045.1:c.1798-7_1800delinsATCGGCTGCT
XM_011545046.1:c.1765-7_1767delinsATCGGCTGCT
XM_011545047.1:c.1798-7_1800delinsATCGGCTGCT
XM_011545048.1:c.1798-7_1800delinsATCGGCTGCT
XM_011545049.1:c.1567-7_1569delinsATCGGCTGCT
XM_011545050.1:c.1540-7_1542delinsATCGGCTGCT
XM_011545051.1:c.1798-7_1800delinsATCGGCTGCT
XM_011545052.1:c.1798-7_1800delinsATCGGCTGCT
XR_949938.1:n.2118-7_2120delinsATCGGCTGCT
XR_949941.1:n.2118-7_2120delinsATCGGCTGCT
XR_949942.1:n.2120-7_2122delinsATCGGCTGCT
XR_949943.1:n.2120-7_2122delinsATCGGCTGCT
XM_011545044.2:c.1798-7_1800delinsATCGGCTGCT
XM_011545046.2:c.1888-7_1890delinsATCGGCTGCT
XM_011545050.2:c.1540-7_1542delinsATCGGCTGCT
XM_017017778.1:c.1888-7_1890delinsATCGGCTGCT
XM_017017779.1:c.1888-7_1890delinsATCGGCTGCT
XM_017017780.1:c.1888-7_1890delinsATCGGCTGCT
XM_017017781.1:c.1888-7_1890delinsATCGGCTGCT
XM_017017782.1:c.1888-7_1890delinsATCGGCTGCT
XM_017017783.1:c.1888-7_1890delinsATCGGCTGCT
XM_017017784.1:c.1888-7_1890delinsATCGGCTGCT
XM_017017785.1:c.1657-7_1659delinsATCGGCTGCT
XM_017017786.1:c.1888-7_1890delinsATCGGCTGCT
XM_017017787.1:c.1888-7_1890delinsATCGGCTGCT
XM_017017788.1:c.1888-7_1890delinsATCGGCTGCT
XR_001747885.1:n.1903-7_1905delinsATCGGCTGCT
XR_001747886.1:n.1903-7_1905delinsATCGGCTGCT
XR_001747887.1:n.1903-7_1905delinsATCGGCTGCT
XR_001747888.1:n.1903-7_1905delinsATCGGCTGCT
XR_001747889.1:n.1903-7_1905delinsATCGGCTGCT
NM_000260.4:c.1798-7_1800delinsATCGGCTGCT
NM_001127180.2:c.1798-7_1800delinsATCGGCTGCT
NM_001369365.1:c.1765-7_1767delinsATCGGCTGCT