Canonical Allele Identifier: CA2203660188

Gene: NAGPA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028964A= , CM000678.2:g.5028964A=	GRCh38
NC_000016.9:g.5078965A= , CM000678.1:g.5078965A=	GRCh37
NC_000016.8:g.5018966A=	NCBI36
NG_028152.1:g.9978T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.836T= MANE Select	ENSP00000310998.3:p.Val279=
ENST00000649828.1:c.836T=	ENSP00000498032.1:p.Val279=
ENST00000312251.7:c.836T=	ENSP00000310998.3:p.Val279=
ENST00000381955.7:c.836T=	ENSP00000371381.3:p.Val279=
ENST00000562037.1:c.597T=	ENSP00000464994.1:n.597T=
ENST00000562346.2:c.505-779T=
ENST00000562746.5:c.836T=	ENSP00000455900.1:p.Val279=
ENST00000563578.5:c.654T=
ENST00000564397.5:n.1195T=
ENST00000565876.5:c.480+1421T=
ENST00000567739.5:n.155T=
ENST00000568202.5:n.699T=
ENST00000569296.5:c.380T=	ENSP00000465949.1:p.Val127=
NM_016256.3:c.836T=	NP_057340.2:p.Val279=
XM_011522517.1:c.836T=	XP_011520819.1:p.Val279=
XM_011522518.1:c.836T=	XP_011520820.1:p.Val279=
XM_011522519.1:c.836T=	XP_011520821.1:p.Val279=
XR_243285.1:n.863T=
XM_011522517.3:c.836T=	XP_011520819.1:p.Val279=
XR_001751908.2:n.862T=
XR_001751909.2:n.862T=
XR_001751910.2:n.862T=
XR_001751911.2:n.862T=
XR_001751912.2:n.862T=
NM_016256.4:c.836T= MANE Select	NP_057340.2:p.Val279=