Canonical Allele Identifier: CA394662902

Gene: NAGPA

Linked Data

• MyVariant Identifiers: chr16:g.5078980A>G (hg19) ; chr16:g.5028979A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028979A>G , CM000678.2:g.5028979A>G	GRCh38
NC_000016.9:g.5078980A>G , CM000678.1:g.5078980A>G	GRCh37
NC_000016.8:g.5018981A>G	NCBI36
NG_028152.1:g.9963T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.821T>C MANE Select	ENSP00000310998.3:p.Leu274Pro
ENST00000649828.1:c.821T>C	ENSP00000498032.1:p.Leu274Pro
ENST00000312251.7:c.821T>C	ENSP00000310998.3:p.Leu274Pro
ENST00000381955.7:c.821T>C	ENSP00000371381.3:p.Leu274Pro
ENST00000562037.1:c.582T>C	ENSP00000464994.1:n.582T>C
ENST00000562346.2:c.505-794T>C
ENST00000562746.5:c.821T>C	ENSP00000455900.1:p.Leu274Pro
ENST00000563578.5:c.639T>C
ENST00000564397.5:n.1180T>C
ENST00000565876.5:c.480+1406T>C
ENST00000567739.5:n.140T>C
ENST00000568202.5:n.684T>C
ENST00000569296.5:c.365T>C	ENSP00000465949.1:p.Leu122Pro
NM_016256.3:c.821T>C	NP_057340.2:p.Leu274Pro
XM_011522517.1:c.821T>C	XP_011520819.1:p.Leu274Pro
XM_011522518.1:c.821T>C	XP_011520820.1:p.Leu274Pro
XM_011522519.1:c.821T>C	XP_011520821.1:p.Leu274Pro
XR_243285.1:n.848T>C
XM_011522517.3:c.821T>C	XP_011520819.1:p.Leu274Pro
XR_001751908.2:n.847T>C
XR_001751909.2:n.847T>C
XR_001751910.2:n.847T>C
XR_001751911.2:n.847T>C
XR_001751912.2:n.847T>C
NM_016256.4:c.821T>C MANE Select	NP_057340.2:p.Leu274Pro