Canonical Allele Identifier: CA2695224487
Gene: MYO15A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18138920_18138921delinsTT , CM000679.2:g.18138920_18138921delinsTT GRCh38
NC_000017.10:g.18042234_18042235delinsTT , CM000679.1:g.18042234_18042235delinsTT GRCh37
NC_000017.9:g.17982959_17982960delinsTT NCBI36
NG_011634.1:g.35215_35216delinsTT
NG_011634.2:g.35215_35216delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646238.1:n.381_382delinsTT
ENST00000647165.2:c.5117_5118delinsTT MANE Select ENSP00000495481.1:p.Gly1706Val
ENST00000205890.9:c.5117_5118delinsTT ENSP00000205890.5:p.Gly1706Val
ENST00000615845.4:c.5117_5118delinsTT ENSP00000481642.1:p.Gly1706Val
NM_016239.3:c.5117_5118delinsTT NP_057323.3:p.Gly1706Val
XM_011523917.1:c.5111_5112delinsTT XP_011522219.1:p.Gly1704Val
XM_011523918.1:c.5111_5112delinsTT XP_011522220.1:p.Gly1704Val
XM_011523919.1:c.5111_5112delinsTT XP_011522221.1:p.Gly1704Val
XM_011523920.1:c.5111_5112delinsTT XP_011522222.1:p.Gly1704Val
XM_011523921.1:c.5111_5112delinsTT XP_011522223.1:p.Gly1704Val
XR_934037.1:n.5770_5771delinsTT
XR_934038.1:n.5770_5771delinsTT
XR_934039.1:n.5770_5771delinsTT
XM_011523918.2:c.5111_5112delinsTT XP_011522220.1:p.Gly1704Val
XM_017024714.2:c.5111_5112delinsTT XP_016880203.1:p.Gly1704Val
XM_017024715.2:c.5120_5121delinsTT XP_016880204.1:p.Gly1707Val
XM_024450780.1:c.5111_5112delinsTT XP_024306548.1:p.Gly1704Val
XM_024450781.1:c.5111_5112delinsTT XP_024306549.1:p.Gly1704Val
XM_024450782.1:c.5111_5112delinsTT XP_024306550.1:p.Gly1704Val
XR_934039.2:n.5809_5810delinsTT
NM_016239.4:c.5117_5118delinsTT MANE Select NP_057323.3:p.Gly1706Val
Search 100 bp 5'
Search 100 bp 3'