Canonical Allele Identifier: CA394187934

Gene: GNPTG

Linked Data

• gnomAD v4: 16-1362305-C-A
• MyVariant Identifiers: chr16:g.1412306C>A (hg19) ; chr16:g.1362305C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362305C>A , CM000678.2:g.1362305C>A	GRCh38
NC_000016.9:g.1412306C>A , CM000678.1:g.1412306C>A	GRCh37
NC_000016.8:g.1352307C>A	NCBI36
NG_016985.1:g.15407C>A
NG_033129.1:g.57400G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.610C>A
ENST00000529110.2:c.595C>A	ENSP00000435349.2:p.Pro199Thr
ENST00000529957.6:n.569C>A
ENST00000683366.1:c.*243C>A	ENSP00000507283.1:n.*243C>A
ENST00000683887.1:c.559C>A	ENSP00000506886.1:p.Pro187Thr
ENST00000684100.1:n.505C>A
ENST00000684126.1:n.569C>A
ENST00000684688.1:n.1136C>A
ENST00000204679.9:c.511C>A MANE Select	ENSP00000204679.4:p.Pro171Thr
ENST00000204679.8:c.511C>A	ENSP00000204679.4:p.Pro171Thr
ENST00000527076.1:n.1527C>A
ENST00000527168.5:n.547C>A
ENST00000529957.5:n.610C>A
NM_032520.4:c.511C>A	NP_115909.1:p.Pro171Thr
XM_017023782.1:c.559C>A	XP_016879271.1:p.Pro187Thr
XM_017023783.1:c.151C>A	XP_016879272.1:p.Pro51Thr
NM_032520.5:c.511C>A MANE Select	NP_115909.1:p.Pro171Thr