Canonical Allele Identifier: CA2203660101

Gene: NAGPA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028906G= , CM000678.2:g.5028906G=	GRCh38
NC_000016.9:g.5078907G= , CM000678.1:g.5078907G=	GRCh37
NC_000016.8:g.5018908G=	NCBI36
NG_028152.1:g.10036C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.894C= MANE Select	ENSP00000310998.3:p.Thr298=
ENST00000649828.1:c.894C=	ENSP00000498032.1:p.Thr298=
ENST00000312251.7:c.894C=	ENSP00000310998.3:p.Thr298=
ENST00000381955.7:c.894C=	ENSP00000371381.3:p.Thr298=
ENST00000562346.2:c.505-721C=
ENST00000562746.5:c.894C=	ENSP00000455900.1:p.Thr298=
ENST00000563578.5:c.712C=
ENST00000564397.5:n.1253C=
ENST00000565876.5:c.480+1479C=
ENST00000567739.5:n.213C=
ENST00000568202.5:n.757C=
ENST00000569296.5:c.438C=	ENSP00000465949.1:p.Thr146=
NM_016256.3:c.894C=	NP_057340.2:p.Thr298=
XM_011522517.1:c.894C=	XP_011520819.1:p.Thr298=
XM_011522518.1:c.894C=	XP_011520820.1:p.Thr298=
XM_011522519.1:c.894C=	XP_011520821.1:p.Thr298=
XR_243285.1:n.921C=
XM_011522517.3:c.894C=	XP_011520819.1:p.Thr298=
XR_001751908.2:n.920C=
XR_001751909.2:n.920C=
XR_001751910.2:n.920C=
XR_001751911.2:n.920C=
XR_001751912.2:n.920C=
NM_016256.4:c.894C= MANE Select	NP_057340.2:p.Thr298=