Canonical Allele Identifier: CA2250848752

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18142238C= , CM000679.2:g.18142238C=	GRCh38
NC_000017.10:g.18045552C= , CM000679.1:g.18045552C=	GRCh37
NC_000017.9:g.17986277C=	NCBI36
NG_011634.1:g.38533C=
NG_011634.2:g.38533C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.5809C= MANE Select	ENSP00000495481.1:p.Arg1937=
ENST00000205890.9:c.5809C=	ENSP00000205890.5:p.Arg1937=
ENST00000615845.4:c.5809C=	ENSP00000481642.1:p.Arg1937=
NM_016239.3:c.5809C=	NP_057323.3:p.Arg1937=
XM_011523917.1:c.5803C=	XP_011522219.1:p.Arg1935=
XM_011523918.1:c.5803C=	XP_011522220.1:p.Arg1935=
XM_011523919.1:c.5803C=	XP_011522221.1:p.Arg1935=
XM_011523920.1:c.5803C=	XP_011522222.1:p.Arg1935=
XM_011523921.1:c.5803C=	XP_011522223.1:p.Arg1935=
XR_934037.1:n.6462C=
XR_934038.1:n.6462C=
XR_934039.1:n.6462C=
XM_011523918.2:c.5803C=	XP_011522220.1:p.Arg1935=
XM_017024714.2:c.5803C=	XP_016880203.1:p.Arg1935=
XM_017024715.2:c.5812C=	XP_016880204.1:p.Arg1938=
XM_024450780.1:c.5803C=	XP_024306548.1:p.Arg1935=
XM_024450781.1:c.5803C=	XP_024306549.1:p.Arg1935=
XM_024450782.1:c.5803C=	XP_024306550.1:p.Arg1935=
XR_934039.2:n.6501C=
NM_016239.4:c.5809C= MANE Select	NP_057323.3:p.Arg1937=