Canonical Allele Identifier: CA394660749

Gene: NAGPA

Linked Data

• MyVariant Identifiers: chr16:g.5078010T>C (hg19) ; chr16:g.5028009T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028009T>C , CM000678.2:g.5028009T>C	GRCh38
NC_000016.9:g.5078010T>C , CM000678.1:g.5078010T>C	GRCh37
NC_000016.8:g.5018011T>C	NCBI36
NG_028152.1:g.10933A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1097A>G MANE Select	ENSP00000310998.3:p.Asn366Ser
ENST00000649828.1:c.*269A>G	ENSP00000498032.1:n.*269A>G
ENST00000312251.7:c.1097A>G	ENSP00000310998.3:p.Asn366Ser
ENST00000381955.7:c.1097A>G	ENSP00000371381.3:p.Asn366Ser
ENST00000562746.5:c.*269A>G	ENSP00000455900.1:n.*269A>G
ENST00000563578.5:c.738+871A>G
ENST00000564397.5:n.2150A>G
ENST00000565876.5:c.481-630A>G
ENST00000566137.5:n.395A>G
ENST00000567739.5:n.416A>G
ENST00000568202.5:n.960A>G
ENST00000569296.5:c.710A>G	ENSP00000465949.1:n.710A>G
NM_016256.3:c.1097A>G	NP_057340.2:p.Asn366Ser
XM_011522517.1:c.1097A>G	XP_011520819.1:p.Asn366Ser
XR_243285.1:n.1193A>G
XM_011522517.3:c.1097A>G	XP_011520819.1:p.Asn366Ser
XR_001751908.2:n.1192A>G
XR_001751909.2:n.1196A>G
XR_001751910.2:n.1225A>G
XR_001751911.2:n.1225A>G
XR_001751912.2:n.1229A>G
NM_016256.4:c.1097A>G MANE Select	NP_057340.2:p.Asn366Ser