Canonical Allele Identifier: CA398606569
Gene: MYO15A HGNC NCBI

Linked Data

dbSNP Id: rs121908965

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145935A>G , CM000679.2:g.18145935A>G GRCh38
NC_000017.10:g.18049249A>G , CM000679.1:g.18049249A>G GRCh37
NC_000017.9:g.17989974A>G NCBI36
NG_011634.1:g.42230A>G
NG_011634.2:g.42230A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6337A>G MANE Select ENSP00000495481.1:p.Ile2113Val
ENST00000205890.9:c.6337A>G ENSP00000205890.5:p.Ile2113Val
ENST00000615845.4:c.6337A>G ENSP00000481642.1:p.Ile2113Val
NM_016239.3:c.6337A>G NP_057323.3:p.Ile2113Val
XM_011523917.1:c.6277A>G XP_011522219.1:p.Ile2093Val
XM_011523918.1:c.6277A>G XP_011522220.1:p.Ile2093Val
XM_011523921.1:c.6331A>G XP_011522223.1:p.Ile2111Val
XR_934037.1:n.6936A>G
XR_934038.1:n.6936A>G
XM_011523918.2:c.6277A>G XP_011522220.1:p.Ile2093Val
XM_017024714.2:c.6277A>G XP_016880203.1:p.Ile2093Val
XM_017024715.2:c.6340A>G XP_016880204.1:p.Ile2114Val
XM_024450781.1:c.6213+1343A>G XP_024306549.1:n.6213+1343A>G
NM_016239.4:c.6337A>G MANE Select NP_057323.3:p.Ile2113Val