Canonical Allele Identifier: CA394663009

Gene: NAGPA

Linked Data

• MyVariant Identifiers: chr16:g.5079002G>T (hg19) ; chr16:g.5029001G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5029001G>T , CM000678.2:g.5029001G>T	GRCh38
NC_000016.9:g.5079002G>T , CM000678.1:g.5079002G>T	GRCh37
NC_000016.8:g.5019003G>T	NCBI36
NG_028152.1:g.9941C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.799C>A MANE Select	ENSP00000310998.3:p.Leu267Met
ENST00000649828.1:c.799C>A	ENSP00000498032.1:p.Leu267Met
ENST00000312251.7:c.799C>A	ENSP00000310998.3:p.Leu267Met
ENST00000381955.7:c.799C>A	ENSP00000371381.3:p.Leu267Met
ENST00000562037.1:c.560C>A	ENSP00000464994.1:n.560C>A
ENST00000562346.2:c.505-816C>A
ENST00000562746.5:c.799C>A	ENSP00000455900.1:p.Leu267Met
ENST00000563578.5:c.617C>A
ENST00000564397.5:n.1158C>A
ENST00000565876.5:c.480+1384C>A
ENST00000567739.5:n.118C>A
ENST00000568202.5:n.662C>A
ENST00000569296.5:c.343C>A	ENSP00000465949.1:p.Leu115Met
NM_016256.3:c.799C>A	NP_057340.2:p.Leu267Met
XM_011522517.1:c.799C>A	XP_011520819.1:p.Leu267Met
XM_011522518.1:c.799C>A	XP_011520820.1:p.Leu267Met
XM_011522519.1:c.799C>A	XP_011520821.1:p.Leu267Met
XR_243285.1:n.826C>A
XM_011522517.3:c.799C>A	XP_011520819.1:p.Leu267Met
XR_001751908.2:n.825C>A
XR_001751909.2:n.825C>A
XR_001751910.2:n.825C>A
XR_001751911.2:n.825C>A
XR_001751912.2:n.825C>A
NM_016256.4:c.799C>A MANE Select	NP_057340.2:p.Leu267Met