Canonical Allele Identifier: CA2015276289

Gene: M6PR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8945266A= , CM000674.2:g.8945266A=	GRCh38
NC_000012.11:g.9097862A= , CM000674.1:g.9097862A=	GRCh37
NC_000012.10:g.8989129A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000000412.8:c.343+152T= MANE Select	ENSP00000000412.3:n.343+152T=
ENST00000000412.7:c.343+152T=	ENSP00000000412.3:n.343+152T=
ENST00000536844.5:c.343+152T=	ENSP00000440488.2:n.343+152T=
ENST00000540837.1:n.619T=
ENST00000541507.5:c.343+152T=	ENSP00000442100.1:n.343+152T=
ENST00000543258.1:c.179+152T=
ENST00000543704.5:c.66+1037T=	ENSP00000437595.1:n.66+1037T=
ENST00000543834.1:n.62+152T=
ENST00000544245.1:c.-12+152T=	ENSP00000439968.1:n.-12+152T=
NM_001207024.1:c.343+152T=	NP_001193953.1:n.343+152T=
NM_002355.3:c.343+152T=	NP_002346.1:n.343+152T=
XM_005253376.1:c.343+152T=	XP_005253433.1:n.343+152T=
XM_011520672.1:c.343+152T=	XP_011518974.1:n.343+152T=
XM_005253376.2:c.343+152T=	XP_005253433.1:n.343+152T=
NM_002355.4:c.343+152T= MANE Select	NP_002346.1:n.343+152T=
NM_001207024.2:c.343+152T=	NP_001193953.1:n.343+152T=