Canonical Allele Identifier: CA394660536

Gene: NAGPA

Linked Data

• dbSNP Id: rs756669461
• gnomAD v3: 16-5027992-G-C
• gnomAD v4: 16-5027992-G-C
• MyVariant Identifiers: chr16:g.5077993G>C (hg19) ; chr16:g.5027992G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5027992G>C , CM000678.2:g.5027992G>C	GRCh38
NC_000016.9:g.5077993G>C , CM000678.1:g.5077993G>C	GRCh37
NC_000016.8:g.5017994G>C	NCBI36
NG_028152.1:g.10950C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1114C>G MANE Select	ENSP00000310998.3:p.Leu372Val
ENST00000649828.1:c.*286C>G	ENSP00000498032.1:n.*286C>G
ENST00000312251.7:c.1114C>G	ENSP00000310998.3:p.Leu372Val
ENST00000381955.7:c.1114C>G	ENSP00000371381.3:p.Leu372Val
ENST00000562746.5:c.*286C>G	ENSP00000455900.1:n.*286C>G
ENST00000563578.5:c.738+888C>G
ENST00000564397.5:n.2167C>G
ENST00000565876.5:c.481-613C>G
ENST00000566137.5:n.412C>G
ENST00000567739.5:n.433C>G
ENST00000568202.5:n.977C>G
ENST00000569296.5:c.727C>G	ENSP00000465949.1:n.727C>G
NM_016256.3:c.1114C>G	NP_057340.2:p.Leu372Val
XM_011522517.1:c.1114C>G	XP_011520819.1:p.Leu372Val
XR_243285.1:n.1210C>G
XM_011522517.3:c.1114C>G	XP_011520819.1:p.Leu372Val
XR_001751908.2:n.1209C>G
XR_001751909.2:n.1213C>G
XR_001751910.2:n.1242C>G
XR_001751911.2:n.1242C>G
XR_001751912.2:n.1246C>G
NM_016256.4:c.1114C>G MANE Select	NP_057340.2:p.Leu372Val