Canonical Allele Identifier: CA394662704

Gene: NAGPA

Linked Data

• MyVariant Identifiers: chr16:g.5078929G>T (hg19) ; chr16:g.5028928G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028928G>T , CM000678.2:g.5028928G>T	GRCh38
NC_000016.9:g.5078929G>T , CM000678.1:g.5078929G>T	GRCh37
NC_000016.8:g.5018930G>T	NCBI36
NG_028152.1:g.10014C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.872C>A MANE Select	ENSP00000310998.3:p.Ala291Asp
ENST00000649828.1:c.872C>A	ENSP00000498032.1:p.Ala291Asp
ENST00000312251.7:c.872C>A	ENSP00000310998.3:p.Ala291Asp
ENST00000381955.7:c.872C>A	ENSP00000371381.3:p.Ala291Asp
ENST00000562346.2:c.505-743C>A
ENST00000562746.5:c.872C>A	ENSP00000455900.1:p.Ala291Asp
ENST00000563578.5:c.690C>A
ENST00000564397.5:n.1231C>A
ENST00000565876.5:c.480+1457C>A
ENST00000567739.5:n.191C>A
ENST00000568202.5:n.735C>A
ENST00000569296.5:c.416C>A	ENSP00000465949.1:p.Ala139Asp
NM_016256.3:c.872C>A	NP_057340.2:p.Ala291Asp
XM_011522517.1:c.872C>A	XP_011520819.1:p.Ala291Asp
XM_011522518.1:c.872C>A	XP_011520820.1:p.Ala291Asp
XM_011522519.1:c.872C>A	XP_011520821.1:p.Ala291Asp
XR_243285.1:n.899C>A
XM_011522517.3:c.872C>A	XP_011520819.1:p.Ala291Asp
XR_001751908.2:n.898C>A
XR_001751909.2:n.898C>A
XR_001751910.2:n.898C>A
XR_001751911.2:n.898C>A
XR_001751912.2:n.898C>A
NM_016256.4:c.872C>A MANE Select	NP_057340.2:p.Ala291Asp