Canonical Allele Identifier: CA394660120

Gene: NAGPA

Linked Data

• MyVariant Identifiers: chr16:g.5077869C>T (hg19) ; chr16:g.5027868C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5027868C>T , CM000678.2:g.5027868C>T	GRCh38
NC_000016.9:g.5077869C>T , CM000678.1:g.5077869C>T	GRCh37
NC_000016.8:g.5017870C>T	NCBI36
NG_028152.1:g.11074G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1152G>A MANE Select	ENSP00000310998.3:p.Trp384Ter
ENST00000649828.1:c.*324G>A	ENSP00000498032.1:n.*324G>A
ENST00000312251.7:c.1152G>A	ENSP00000310998.3:p.Trp384Ter
ENST00000381955.7:c.1152G>A	ENSP00000371381.3:p.Trp384Ter
ENST00000562746.5:c.*324G>A	ENSP00000455900.1:n.*324G>A
ENST00000563578.5:c.738+1012G>A
ENST00000564397.5:n.2205G>A
ENST00000565876.5:c.481-489G>A
ENST00000566137.5:n.450G>A
ENST00000567739.5:n.471G>A
ENST00000568202.5:n.1015G>A
ENST00000569296.5:c.765G>A	ENSP00000465949.1:n.765G>A
NM_016256.3:c.1152G>A	NP_057340.2:p.Trp384Ter
XM_011522517.1:c.1152G>A	XP_011520819.1:p.Trp384Ter
XR_243285.1:n.1248G>A
XM_011522517.3:c.1152G>A	XP_011520819.1:p.Trp384Ter
XR_001751908.2:n.1247G>A
XR_001751909.2:n.1251G>A
XR_001751910.2:n.1280G>A
XR_001751911.2:n.1280G>A
XR_001751912.2:n.1284G>A
NM_016256.4:c.1152G>A MANE Select	NP_057340.2:p.Trp384Ter