Canonical Allele Identifier: CA620700223

Gene: GNPTG

Linked Data

• dbSNP Id: rs1337585208
• gnomAD v2: 16-1412373-C-T
• gnomAD v3: 16-1362372-C-T
• gnomAD v4: 16-1362372-C-T
• MyVariant Identifiers: chr16:g.1412373C>T (hg19) ; chr16:g.1362372C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362372C>T , CM000678.2:g.1362372C>T	GRCh38
NC_000016.9:g.1412373C>T , CM000678.1:g.1412373C>T	GRCh37
NC_000016.8:g.1352374C>T	NCBI36
NG_016985.1:g.15474C>T
NG_033129.1:g.57333G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.625+52C>T
ENST00000529110.2:c.610+52C>T	ENSP00000435349.2:n.610+52C>T
ENST00000529957.6:n.584+52C>T
ENST00000683366.1:c.*258+52C>T	ENSP00000507283.1:n.*258+52C>T
ENST00000683887.1:c.574+52C>T	ENSP00000506886.1:n.574+52C>T
ENST00000684100.1:n.520+52C>T
ENST00000684126.1:n.584+52C>T
ENST00000684688.1:n.1151+52C>T
ENST00000204679.9:c.526+52C>T MANE Select	ENSP00000204679.4:n.526+52C>T
ENST00000204679.8:c.526+52C>T	ENSP00000204679.4:n.526+52C>T
ENST00000527076.1:n.1594C>T
ENST00000527168.5:n.614C>T
ENST00000529957.5:n.625+52C>T
NM_032520.4:c.526+52C>T	NP_115909.1:n.526+52C>T
XM_017023782.1:c.574+52C>T	XP_016879271.1:n.574+52C>T
XM_017023783.1:c.166+52C>T	XP_016879272.1:n.166+52C>T
NM_032520.5:c.526+52C>T MANE Select	NP_115909.1:n.526+52C>T