Canonical Allele Identifier: CA2250850288

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18145867C= , CM000679.2:g.18145867C=	GRCh38
NC_000017.10:g.18049181C= , CM000679.1:g.18049181C=	GRCh37
NC_000017.9:g.17989906C=	NCBI36
NG_011634.1:g.42162C=
NG_011634.2:g.42162C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6274-5C= MANE Select	ENSP00000495481.1:n.6274-5C=
ENST00000205890.9:c.6274-5C=	ENSP00000205890.5:n.6274-5C=
ENST00000615845.4:c.6274-5C=	ENSP00000481642.1:n.6274-5C=
NM_016239.3:c.6274-5C=	NP_057323.3:n.6274-5C=
XM_011523917.1:c.6214-5C=	XP_011522219.1:n.6214-5C=
XM_011523918.1:c.6214-5C=	XP_011522220.1:n.6214-5C=
XM_011523921.1:c.6268-5C=	XP_011522223.1:n.6268-5C=
XR_934037.1:n.6873-5C=
XR_934038.1:n.6873-5C=
XM_011523918.2:c.6214-5C=	XP_011522220.1:n.6214-5C=
XM_017024714.2:c.6214-5C=	XP_016880203.1:n.6214-5C=
XM_017024715.2:c.6277-5C=	XP_016880204.1:n.6277-5C=
XM_024450781.1:c.6213+1275C=	XP_024306549.1:n.6213+1275C=
NM_016239.4:c.6274-5C= MANE Select	NP_057323.3:n.6274-5C=