Canonical Allele Identifier: CA718228660

Gene: GNPTG

Linked Data

• dbSNP Id: rs1220156587
• gnomAD v3: 16-1362392-G-A
• gnomAD v4: 16-1362392-G-A
• MyVariant Identifiers: chr16:g.1412393G>A (hg19) ; chr16:g.1362392G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362392G>A , CM000678.2:g.1362392G>A	GRCh38
NC_000016.9:g.1412393G>A , CM000678.1:g.1412393G>A	GRCh37
NC_000016.8:g.1352394G>A	NCBI36
NG_016985.1:g.15494G>A
NG_033129.1:g.57313C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.626-60G>A
ENST00000529110.2:c.611-60G>A	ENSP00000435349.2:n.611-60G>A
ENST00000529957.6:n.585-60G>A
ENST00000683366.1:c.*259-60G>A	ENSP00000507283.1:n.*259-60G>A
ENST00000683887.1:c.575-60G>A	ENSP00000506886.1:n.575-60G>A
ENST00000684100.1:n.521-60G>A
ENST00000684126.1:n.585-60G>A
ENST00000684688.1:n.1152-60G>A
ENST00000204679.9:c.527-60G>A MANE Select	ENSP00000204679.4:n.527-60G>A
ENST00000204679.8:c.527-60G>A	ENSP00000204679.4:n.527-60G>A
ENST00000527076.1:n.1614G>A
ENST00000527168.5:n.634G>A
ENST00000529957.5:n.626-60G>A
NM_032520.4:c.527-60G>A	NP_115909.1:n.527-60G>A
XM_017023782.1:c.575-60G>A	XP_016879271.1:n.575-60G>A
XM_017023783.1:c.167-60G>A	XP_016879272.1:n.167-60G>A
NM_032520.5:c.527-60G>A MANE Select	NP_115909.1:n.527-60G>A