Canonical Allele Identifier: CA2203660178

Gene: NAGPA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028960G= , CM000678.2:g.5028960G=	GRCh38
NC_000016.9:g.5078961G= , CM000678.1:g.5078961G=	GRCh37
NC_000016.8:g.5018962G=	NCBI36
NG_028152.1:g.9982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.840C= MANE Select	ENSP00000310998.3:p.Val280=
ENST00000649828.1:c.840C=	ENSP00000498032.1:p.Val280=
ENST00000312251.7:c.840C=	ENSP00000310998.3:p.Val280=
ENST00000381955.7:c.840C=	ENSP00000371381.3:p.Val280=
ENST00000562037.1:c.601C=	ENSP00000464994.1:n.601C=
ENST00000562346.2:c.505-775C=
ENST00000562746.5:c.840C=	ENSP00000455900.1:p.Val280=
ENST00000563578.5:c.658C=
ENST00000564397.5:n.1199C=
ENST00000565876.5:c.480+1425C=
ENST00000567739.5:n.159C=
ENST00000568202.5:n.703C=
ENST00000569296.5:c.384C=	ENSP00000465949.1:p.Val128=
NM_016256.3:c.840C=	NP_057340.2:p.Val280=
XM_011522517.1:c.840C=	XP_011520819.1:p.Val280=
XM_011522518.1:c.840C=	XP_011520820.1:p.Val280=
XM_011522519.1:c.840C=	XP_011520821.1:p.Val280=
XR_243285.1:n.867C=
XM_011522517.3:c.840C=	XP_011520819.1:p.Val280=
XR_001751908.2:n.866C=
XR_001751909.2:n.866C=
XR_001751910.2:n.866C=
XR_001751911.2:n.866C=
XR_001751912.2:n.866C=
NM_016256.4:c.840C= MANE Select	NP_057340.2:p.Val280=