Canonical Allele Identifier: CA2630958150

Gene: GNPTG

Linked Data

• gnomAD v4: 16-1361698-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361698G>A , CM000678.2:g.1361698G>A	GRCh38
NC_000016.9:g.1411699G>A , CM000678.1:g.1411699G>A	GRCh37
NC_000016.8:g.1351700G>A	NCBI36
NG_016985.1:g.14800G>A
NG_033129.1:g.58007C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.278-45G>A
ENST00000529110.2:c.263-45G>A	ENSP00000435349.2:n.263-45G>A
ENST00000529957.6:n.237-45G>A
ENST00000683366.1:c.179-174G>A	ENSP00000507283.1:n.179-174G>A
ENST00000683887.1:c.182G>A	ENSP00000506886.1:p.Arg61Lys
ENST00000684100.1:n.54G>A
ENST00000684126.1:n.237-45G>A
ENST00000684688.1:n.759G>A
ENST00000204679.9:c.179-45G>A MANE Select	ENSP00000204679.4:n.179-45G>A
ENST00000204679.8:c.179-45G>A	ENSP00000204679.4:n.179-45G>A
ENST00000526820.5:c.*81-45G>A	ENSP00000434413.1:n.*81-45G>A
ENST00000527076.1:n.1076G>A
ENST00000527168.5:n.270-174G>A
ENST00000529110.1:c.246-45G>A
ENST00000529957.5:n.278-45G>A
NM_032520.4:c.179-45G>A	NP_115909.1:n.179-45G>A
XM_017023782.1:c.182G>A	XP_016879271.1:p.Arg61Lys
XM_017023783.1:c.-182-45G>A	XP_016879272.1:n.-182-45G>A
NM_032520.5:c.179-45G>A MANE Select	NP_115909.1:n.179-45G>A