Canonical Allele Identifier: CA398606444
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049220G>C (hg19) chr17:g.18145906G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145906G>C , CM000679.2:g.18145906G>C GRCh38
NC_000017.10:g.18049220G>C , CM000679.1:g.18049220G>C GRCh37
NC_000017.9:g.17989945G>C NCBI36
NG_011634.1:g.42201G>C
NG_011634.2:g.42201G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6308G>C MANE Select ENSP00000495481.1:p.Gly2103Ala
ENST00000205890.9:c.6308G>C ENSP00000205890.5:p.Gly2103Ala
ENST00000615845.4:c.6308G>C ENSP00000481642.1:p.Gly2103Ala
NM_016239.3:c.6308G>C NP_057323.3:p.Gly2103Ala
XM_011523917.1:c.6248G>C XP_011522219.1:p.Gly2083Ala
XM_011523918.1:c.6248G>C XP_011522220.1:p.Gly2083Ala
XM_011523921.1:c.6302G>C XP_011522223.1:p.Gly2101Ala
XR_934037.1:n.6907G>C
XR_934038.1:n.6907G>C
XM_011523918.2:c.6248G>C XP_011522220.1:p.Gly2083Ala
XM_017024714.2:c.6248G>C XP_016880203.1:p.Gly2083Ala
XM_017024715.2:c.6311G>C XP_016880204.1:p.Gly2104Ala
XM_024450781.1:c.6213+1314G>C XP_024306549.1:n.6213+1314G>C
NM_016239.4:c.6308G>C MANE Select NP_057323.3:p.Gly2103Ala
Search 100 bp 5'
Search 100 bp 3'