Canonical Allele Identifier: CA7888570

Gene: NAGPA

Linked Data

• dbSNP Id: rs780932777
• ExAC: 16:5078015 G / C
• gnomAD v2: 16-5078015-G-C
• gnomAD v4: 16-5028014-G-C
• MyVariant Identifiers: chr16:g.5078015G>C (hg19) ; chr16:g.5028014G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028014G>C , CM000678.2:g.5028014G>C	GRCh38
NC_000016.9:g.5078015G>C , CM000678.1:g.5078015G>C	GRCh37
NC_000016.8:g.5018016G>C	NCBI36
NG_028152.1:g.10928C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1092C>G MANE Select	ENSP00000310998.3:p.Pro364=
ENST00000649828.1:c.*264C>G	ENSP00000498032.1:n.*264C>G
ENST00000312251.7:c.1092C>G	ENSP00000310998.3:p.Pro364=
ENST00000381955.7:c.1092C>G	ENSP00000371381.3:p.Pro364=
ENST00000562746.5:c.*264C>G	ENSP00000455900.1:n.*264C>G
ENST00000563578.5:c.738+866C>G
ENST00000564397.5:n.2145C>G
ENST00000565876.5:c.481-635C>G
ENST00000566137.5:n.390C>G
ENST00000567739.5:n.411C>G
ENST00000568202.5:n.955C>G
ENST00000569296.5:c.705C>G	ENSP00000465949.1:n.705C>G
NM_016256.3:c.1092C>G	NP_057340.2:p.Pro364=
XM_011522517.1:c.1092C>G	XP_011520819.1:p.Pro364=
XR_243285.1:n.1188C>G
XM_011522517.3:c.1092C>G	XP_011520819.1:p.Pro364=
XR_001751908.2:n.1187C>G
XR_001751909.2:n.1191C>G
XR_001751910.2:n.1220C>G
XR_001751911.2:n.1220C>G
XR_001751912.2:n.1224C>G
NM_016256.4:c.1092C>G MANE Select	NP_057340.2:p.Pro364=