Canonical Allele Identifier: CA394660754

Gene: NAGPA

Linked Data

• MyVariant Identifiers: chr16:g.5078011T>A (hg19) ; chr16:g.5028010T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.5028010T>A , CM000678.2:g.5028010T>A	GRCh38
NC_000016.9:g.5078011T>A , CM000678.1:g.5078011T>A	GRCh37
NC_000016.8:g.5018012T>A	NCBI36
NG_028152.1:g.10932A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312251.8:c.1096A>T MANE Select	ENSP00000310998.3:p.Asn366Tyr
ENST00000649828.1:c.*268A>T	ENSP00000498032.1:n.*268A>T
ENST00000312251.7:c.1096A>T	ENSP00000310998.3:p.Asn366Tyr
ENST00000381955.7:c.1096A>T	ENSP00000371381.3:p.Asn366Tyr
ENST00000562746.5:c.*268A>T	ENSP00000455900.1:n.*268A>T
ENST00000563578.5:c.738+870A>T
ENST00000564397.5:n.2149A>T
ENST00000565876.5:c.481-631A>T
ENST00000566137.5:n.394A>T
ENST00000567739.5:n.415A>T
ENST00000568202.5:n.959A>T
ENST00000569296.5:c.709A>T	ENSP00000465949.1:n.709A>T
NM_016256.3:c.1096A>T	NP_057340.2:p.Asn366Tyr
XM_011522517.1:c.1096A>T	XP_011520819.1:p.Asn366Tyr
XR_243285.1:n.1192A>T
XM_011522517.3:c.1096A>T	XP_011520819.1:p.Asn366Tyr
XR_001751908.2:n.1191A>T
XR_001751909.2:n.1195A>T
XR_001751910.2:n.1224A>T
XR_001751911.2:n.1224A>T
XR_001751912.2:n.1228A>T
NM_016256.4:c.1096A>T MANE Select	NP_057340.2:p.Asn366Tyr