Canonical Allele Identifier: CA2203674061

Gene: NAGPA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028041G= , CM000678.2:g.5028041G=	GRCh38
NC_000016.9:g.5078042G= , CM000678.1:g.5078042G=	GRCh37
NC_000016.8:g.5018043G=	NCBI36
NG_028152.1:g.10901C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1065C= MANE Select	ENSP00000310998.3:p.Pro355=
ENST00000649828.1:c.*237C=	ENSP00000498032.1:n.*237C=
ENST00000312251.7:c.1065C=	ENSP00000310998.3:p.Pro355=
ENST00000381955.7:c.1065C=	ENSP00000371381.3:p.Pro355=
ENST00000562746.5:c.*237C=	ENSP00000455900.1:n.*237C=
ENST00000563578.5:c.738+839C=
ENST00000564397.5:n.2118C=
ENST00000565876.5:c.481-662C=
ENST00000566137.5:n.363C=
ENST00000567739.5:n.384C=
ENST00000568202.5:n.928C=
ENST00000569296.5:c.678C=	ENSP00000465949.1:n.678C=
NM_016256.3:c.1065C=	NP_057340.2:p.Pro355=
XM_011522517.1:c.1065C=	XP_011520819.1:p.Pro355=
XR_243285.1:n.1161C=
XM_011522517.3:c.1065C=	XP_011520819.1:p.Pro355=
XR_001751908.2:n.1160C=
XR_001751909.2:n.1164C=
XR_001751910.2:n.1193C=
XR_001751911.2:n.1193C=
XR_001751912.2:n.1197C=
NM_016256.4:c.1065C= MANE Select	NP_057340.2:p.Pro355=