Canonical Allele Identifier: CA2203673886

Gene: NAGPA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5027938G= , CM000678.2:g.5027938G=	GRCh38
NC_000016.9:g.5077939G= , CM000678.1:g.5077939G=	GRCh37
NC_000016.8:g.5017940G=	NCBI36
NG_028152.1:g.11004C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1126+42C= MANE Select	ENSP00000310998.3:n.1126+42C=
ENST00000649828.1:c.*298+42C=	ENSP00000498032.1:n.*298+42C=
ENST00000312251.7:c.1126+42C=	ENSP00000310998.3:n.1126+42C=
ENST00000381955.7:c.1126+42C=	ENSP00000371381.3:n.1126+42C=
ENST00000562746.5:c.*298+42C=	ENSP00000455900.1:n.*298+42C=
ENST00000563578.5:c.738+942C=
ENST00000564397.5:n.2179+42C=
ENST00000565876.5:c.481-559C=
ENST00000566137.5:n.424+42C=
ENST00000567739.5:n.445+42C=
ENST00000568202.5:n.989+42C=
ENST00000569296.5:c.739+42C=	ENSP00000465949.1:n.739+42C=
NM_016256.3:c.1126+42C=	NP_057340.2:n.1126+42C=
XM_011522517.1:c.1126+42C=	XP_011520819.1:n.1126+42C=
XR_243285.1:n.1222+42C=
XM_011522517.3:c.1126+42C=	XP_011520819.1:n.1126+42C=
XR_001751908.2:n.1221+42C=
XR_001751909.2:n.1225+42C=
XR_001751910.2:n.1254+42C=
XR_001751911.2:n.1254+42C=
XR_001751912.2:n.1258+42C=
NM_016256.4:c.1126+42C= MANE Select	NP_057340.2:n.1126+42C=