Canonical Allele Identifier: CA394662944

Gene: NAGPA

Linked Data

• MyVariant Identifiers: chr16:g.5078989G>C (hg19) ; chr16:g.5028988G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028988G>C , CM000678.2:g.5028988G>C	GRCh38
NC_000016.9:g.5078989G>C , CM000678.1:g.5078989G>C	GRCh37
NC_000016.8:g.5018990G>C	NCBI36
NG_028152.1:g.9954C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.812C>G MANE Select	ENSP00000310998.3:p.Ala271Gly
ENST00000649828.1:c.812C>G	ENSP00000498032.1:p.Ala271Gly
ENST00000312251.7:c.812C>G	ENSP00000310998.3:p.Ala271Gly
ENST00000381955.7:c.812C>G	ENSP00000371381.3:p.Ala271Gly
ENST00000562037.1:c.573C>G	ENSP00000464994.1:n.573C>G
ENST00000562346.2:c.505-803C>G
ENST00000562746.5:c.812C>G	ENSP00000455900.1:p.Ala271Gly
ENST00000563578.5:c.630C>G
ENST00000564397.5:n.1171C>G
ENST00000565876.5:c.480+1397C>G
ENST00000567739.5:n.131C>G
ENST00000568202.5:n.675C>G
ENST00000569296.5:c.356C>G	ENSP00000465949.1:p.Ala119Gly
NM_016256.3:c.812C>G	NP_057340.2:p.Ala271Gly
XM_011522517.1:c.812C>G	XP_011520819.1:p.Ala271Gly
XM_011522518.1:c.812C>G	XP_011520820.1:p.Ala271Gly
XM_011522519.1:c.812C>G	XP_011520821.1:p.Ala271Gly
XR_243285.1:n.839C>G
XM_011522517.3:c.812C>G	XP_011520819.1:p.Ala271Gly
XR_001751908.2:n.838C>G
XR_001751909.2:n.838C>G
XR_001751910.2:n.838C>G
XR_001751911.2:n.838C>G
XR_001751912.2:n.838C>G
NM_016256.4:c.812C>G MANE Select	NP_057340.2:p.Ala271Gly