Canonical Allele Identifier: CA2203673692

Gene: NAGPA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5027808A= , CM000678.2:g.5027808A=	GRCh38
NC_000016.9:g.5077809A= , CM000678.1:g.5077809A=	GRCh37
NC_000016.8:g.5017810A=	NCBI36
NG_028152.1:g.11134T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1174+38T= MANE Select	ENSP00000310998.3:n.1174+38T=
ENST00000649828.1:c.*346+38T=	ENSP00000498032.1:n.*346+38T=
ENST00000312251.7:c.1174+38T=	ENSP00000310998.3:n.1174+38T=
ENST00000381955.7:c.1174+38T=	ENSP00000371381.3:n.1174+38T=
ENST00000562746.5:c.*346+38T=	ENSP00000455900.1:n.*346+38T=
ENST00000563578.5:c.738+1072T=
ENST00000564397.5:n.2227+38T=
ENST00000565876.5:c.481-429T=
ENST00000566137.5:n.472+38T=
ENST00000567739.5:n.493+38T=
ENST00000568202.5:n.1037+38T=
ENST00000569296.5:c.787+38T=	ENSP00000465949.1:n.787+38T=
NM_016256.3:c.1174+38T=	NP_057340.2:n.1174+38T=
XM_011522517.1:c.1174+38T=	XP_011520819.1:n.1174+38T=
XR_243285.1:n.1270+38T=
XM_011522517.3:c.1174+38T=	XP_011520819.1:n.1174+38T=
XR_001751908.2:n.1269+38T=
XR_001751909.2:n.1273+38T=
XR_001751910.2:n.1302+38T=
XR_001751911.2:n.1302+38T=
XR_001751912.2:n.1306+38T=
NM_016256.4:c.1174+38T= MANE Select	NP_057340.2:n.1174+38T=