Canonical Allele Identifier: CA2250852160

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150361T= , CM000679.2:g.18150361T=	GRCh38
NC_000017.10:g.18053675T= , CM000679.1:g.18053675T=	GRCh37
NC_000017.9:g.17994400T=	NCBI36
NG_011634.1:g.46656T=
NG_011634.2:g.46656T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.7213-68T= MANE Select	ENSP00000495481.1:n.7213-68T=
ENST00000205890.9:c.7213-68T=	ENSP00000205890.5:n.7213-68T=
ENST00000615845.4:c.7213-68T=	ENSP00000481642.1:n.7213-68T=
NM_016239.3:c.7213-68T=	NP_057323.3:n.7213-68T=
XM_011523917.1:c.6888-68T=	XP_011522219.1:n.6888-68T=
XM_011523921.1:c.7207-68T=	XP_011522223.1:n.7207-68T=
XR_934037.1:n.7547-68T=
XR_934038.1:n.7499-68T=
XR_934293.1:n.434+1242A=
XR_934294.1:n.435-588A=
XR_934295.1:n.253+1242A=
XM_017024714.2:c.7153-68T=	XP_016880203.1:n.7153-68T=
XM_017024715.2:c.7216-68T=	XP_016880204.1:n.7216-68T=
XR_934293.2:n.377+1242A=
XR_934294.2:n.378-588A=
NM_016239.4:c.7213-68T= MANE Select	NP_057323.3:n.7213-68T=