Canonical Allele Identifier: CA7888680

Gene: NAGPA

Linked Data

• dbSNP Id: rs772676182
• ExAC: 16:5078957 C / T
• gnomAD v2: 16-5078957-C-T
• gnomAD v3: 16-5028956-C-T
• gnomAD v4: 16-5028956-C-T
• MyVariant Identifiers: chr16:g.5078957C>T (hg19) ; chr16:g.5028956C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028956C>T , CM000678.2:g.5028956C>T	GRCh38
NC_000016.9:g.5078957C>T , CM000678.1:g.5078957C>T	GRCh37
NC_000016.8:g.5018958C>T	NCBI36
NG_028152.1:g.9986G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.844G>A MANE Select	ENSP00000310998.3:p.Ala282Thr
ENST00000649828.1:c.844G>A	ENSP00000498032.1:p.Ala282Thr
ENST00000312251.7:c.844G>A	ENSP00000310998.3:p.Ala282Thr
ENST00000381955.7:c.844G>A	ENSP00000371381.3:p.Ala282Thr
ENST00000562037.1:c.605G>A	ENSP00000464994.1:n.605G>A
ENST00000562346.2:c.505-771G>A
ENST00000562746.5:c.844G>A	ENSP00000455900.1:p.Ala282Thr
ENST00000563578.5:c.662G>A
ENST00000564397.5:n.1203G>A
ENST00000565876.5:c.480+1429G>A
ENST00000567739.5:n.163G>A
ENST00000568202.5:n.707G>A
ENST00000569296.5:c.388G>A	ENSP00000465949.1:p.Ala130Thr
NM_016256.3:c.844G>A	NP_057340.2:p.Ala282Thr
XM_011522517.1:c.844G>A	XP_011520819.1:p.Ala282Thr
XM_011522518.1:c.844G>A	XP_011520820.1:p.Ala282Thr
XM_011522519.1:c.844G>A	XP_011520821.1:p.Ala282Thr
XR_243285.1:n.871G>A
XM_011522517.3:c.844G>A	XP_011520819.1:p.Ala282Thr
XR_001751908.2:n.870G>A
XR_001751909.2:n.870G>A
XR_001751910.2:n.870G>A
XR_001751911.2:n.870G>A
XR_001751912.2:n.870G>A
NM_016256.4:c.844G>A MANE Select	NP_057340.2:p.Ala282Thr