Canonical Allele Identifier: CA8424559
Gene: MYO15A HGNC NCBI

Linked Data

dbSNP Id: rs143720564

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145888G>A , CM000679.2:g.18145888G>A GRCh38
NC_000017.10:g.18049202G>A , CM000679.1:g.18049202G>A GRCh37
NC_000017.9:g.17989927G>A NCBI36
NG_011634.1:g.42183G>A
NG_011634.2:g.42183G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6290G>A MANE Select ENSP00000495481.1:p.Gly2097Asp
ENST00000205890.9:c.6290G>A ENSP00000205890.5:p.Gly2097Asp
ENST00000615845.4:c.6290G>A ENSP00000481642.1:p.Gly2097Asp
NM_016239.3:c.6290G>A NP_057323.3:p.Gly2097Asp
XM_011523917.1:c.6230G>A XP_011522219.1:p.Gly2077Asp
XM_011523918.1:c.6230G>A XP_011522220.1:p.Gly2077Asp
XM_011523921.1:c.6284G>A XP_011522223.1:p.Gly2095Asp
XR_934037.1:n.6889G>A
XR_934038.1:n.6889G>A
XM_011523918.2:c.6230G>A XP_011522220.1:p.Gly2077Asp
XM_017024714.2:c.6230G>A XP_016880203.1:p.Gly2077Asp
XM_017024715.2:c.6293G>A XP_016880204.1:p.Gly2098Asp
XM_024450781.1:c.6213+1296G>A XP_024306549.1:n.6213+1296G>A
NM_016239.4:c.6290G>A MANE Select NP_057323.3:p.Gly2097Asp