Canonical Allele Identifier: CA2552138780

Gene: GNPTG

Linked Data

• gnomAD v4: 16-1362323-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362323A>G , CM000678.2:g.1362323A>G	GRCh38
NC_000016.9:g.1412324A>G , CM000678.1:g.1412324A>G	GRCh37
NC_000016.8:g.1352325A>G	NCBI36
NG_016985.1:g.15425A>G
NG_033129.1:g.57382T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.625+3A>G
ENST00000529110.2:c.610+3A>G	ENSP00000435349.2:n.610+3A>G
ENST00000529957.6:n.584+3A>G
ENST00000683366.1:c.*258+3A>G	ENSP00000507283.1:n.*258+3A>G
ENST00000683887.1:c.574+3A>G	ENSP00000506886.1:n.574+3A>G
ENST00000684100.1:n.520+3A>G
ENST00000684126.1:n.584+3A>G
ENST00000684688.1:n.1151+3A>G
ENST00000204679.9:c.526+3A>G MANE Select	ENSP00000204679.4:n.526+3A>G
ENST00000204679.8:c.526+3A>G	ENSP00000204679.4:n.526+3A>G
ENST00000527076.1:n.1545A>G
ENST00000527168.5:n.565A>G
ENST00000529957.5:n.625+3A>G
NM_032520.4:c.526+3A>G	NP_115909.1:n.526+3A>G
XM_017023782.1:c.574+3A>G	XP_016879271.1:n.574+3A>G
XM_017023783.1:c.166+3A>G	XP_016879272.1:n.166+3A>G
NM_032520.5:c.526+3A>G MANE Select	NP_115909.1:n.526+3A>G