Canonical Allele Identifier: CA2203674057

Gene: NAGPA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028040C= , CM000678.2:g.5028040C=	GRCh38
NC_000016.9:g.5078041C= , CM000678.1:g.5078041C=	GRCh37
NC_000016.8:g.5018042C=	NCBI36
NG_028152.1:g.10902G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1066G= MANE Select	ENSP00000310998.3:p.Gly356=
ENST00000649828.1:c.*238G=	ENSP00000498032.1:n.*238G=
ENST00000312251.7:c.1066G=	ENSP00000310998.3:p.Gly356=
ENST00000381955.7:c.1066G=	ENSP00000371381.3:p.Gly356=
ENST00000562746.5:c.*238G=	ENSP00000455900.1:n.*238G=
ENST00000563578.5:c.738+840G=
ENST00000564397.5:n.2119G=
ENST00000565876.5:c.481-661G=
ENST00000566137.5:n.364G=
ENST00000567739.5:n.385G=
ENST00000568202.5:n.929G=
ENST00000569296.5:c.679G=	ENSP00000465949.1:n.679G=
NM_016256.3:c.1066G=	NP_057340.2:p.Gly356=
XM_011522517.1:c.1066G=	XP_011520819.1:p.Gly356=
XR_243285.1:n.1162G=
XM_011522517.3:c.1066G=	XP_011520819.1:p.Gly356=
XR_001751908.2:n.1161G=
XR_001751909.2:n.1165G=
XR_001751910.2:n.1194G=
XR_001751911.2:n.1194G=
XR_001751912.2:n.1198G=
NM_016256.4:c.1066G= MANE Select	NP_057340.2:p.Gly356=