Canonical Allele Identifier: CA2250850323

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18145942A= , CM000679.2:g.18145942A=	GRCh38
NC_000017.10:g.18049256A= , CM000679.1:g.18049256A=	GRCh37
NC_000017.9:g.17989981A=	NCBI36
NG_011634.1:g.42237A=
NG_011634.2:g.42237A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6344A= MANE Select	ENSP00000495481.1:p.Gln2115=
ENST00000205890.9:c.6344A=	ENSP00000205890.5:p.Gln2115=
ENST00000615845.4:c.6344A=	ENSP00000481642.1:p.Gln2115=
NM_016239.3:c.6344A=	NP_057323.3:p.Gln2115=
XM_011523917.1:c.6284A=	XP_011522219.1:p.Gln2095=
XM_011523918.1:c.6284A=	XP_011522220.1:p.Gln2095=
XM_011523921.1:c.6338A=	XP_011522223.1:p.Gln2113=
XR_934037.1:n.6943A=
XR_934038.1:n.6943A=
XM_011523918.2:c.6284A=	XP_011522220.1:p.Gln2095=
XM_017024714.2:c.6284A=	XP_016880203.1:p.Gln2095=
XM_017024715.2:c.6347A=	XP_016880204.1:p.Gln2116=
XM_024450781.1:c.6213+1350A=	XP_024306549.1:n.6213+1350A=
NM_016239.4:c.6344A= MANE Select	NP_057323.3:p.Gln2115=