Canonical Allele Identifier: CA2203673362

Gene: NAGPA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5027570G= , CM000678.2:g.5027570G=	GRCh38
NC_000016.9:g.5077571G= , CM000678.1:g.5077571G=	GRCh37
NC_000016.8:g.5017572G=	NCBI36
NG_028152.1:g.11372C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1175-191C= MANE Select	ENSP00000310998.3:n.1175-191C=
ENST00000649828.1:c.*347-191C=	ENSP00000498032.1:n.*347-191C=
ENST00000312251.7:c.1175-191C=	ENSP00000310998.3:n.1175-191C=
ENST00000381955.7:c.1174+276C=	ENSP00000371381.3:n.1174+276C=
ENST00000562746.5:c.*347-191C=	ENSP00000455900.1:n.*347-191C=
ENST00000563578.5:c.738+1310C=
ENST00000564397.5:n.2228-191C=
ENST00000565876.5:c.481-191C=
ENST00000566137.5:n.473-191C=
ENST00000567739.5:n.494-191C=
ENST00000568202.5:n.1038-191C=
ENST00000569296.5:c.788-191C=	ENSP00000465949.1:n.788-191C=
NM_016256.3:c.1175-191C=	NP_057340.2:n.1175-191C=
XM_011522517.1:c.1175-191C=	XP_011520819.1:n.1175-191C=
XR_243285.1:n.1271-191C=
XM_011522517.3:c.1175-191C=	XP_011520819.1:n.1175-191C=
XR_001751908.2:n.1270-191C=
XR_001751909.2:n.1274-191C=
XR_001751910.2:n.1303-191C=
XR_001751911.2:n.1303-191C=
XR_001751912.2:n.1307-191C=
NM_016256.4:c.1175-191C= MANE Select	NP_057340.2:n.1175-191C=