Canonical Allele Identifier: CA394187695

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412232A>C (hg19) ; chr16:g.1362231A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362231A>C , CM000678.2:g.1362231A>C	GRCh38
NC_000016.9:g.1412232A>C , CM000678.1:g.1412232A>C	GRCh37
NC_000016.8:g.1352233A>C	NCBI36
NG_016985.1:g.15333A>C
NG_033129.1:g.57474T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.536A>C
ENST00000529110.2:c.521A>C	ENSP00000435349.2:p.Asn174Thr
ENST00000529957.6:n.495A>C
ENST00000683366.1:c.*169A>C	ENSP00000507283.1:n.*169A>C
ENST00000683887.1:c.485A>C	ENSP00000506886.1:p.Asn162Thr
ENST00000684100.1:n.431A>C
ENST00000684126.1:n.495A>C
ENST00000684688.1:n.1062A>C
ENST00000204679.9:c.437A>C MANE Select	ENSP00000204679.4:p.Asn146Thr
ENST00000204679.8:c.437A>C	ENSP00000204679.4:p.Asn146Thr
ENST00000527076.1:n.1453A>C
ENST00000527168.5:n.473A>C
ENST00000529110.1:c.504A>C
ENST00000529957.5:n.536A>C
NM_032520.4:c.437A>C	NP_115909.1:p.Asn146Thr
XM_017023782.1:c.485A>C	XP_016879271.1:p.Asn162Thr
XM_017023783.1:c.77A>C	XP_016879272.1:p.Asn26Thr
NM_032520.5:c.437A>C MANE Select	NP_115909.1:p.Asn146Thr