Canonical Allele Identifier: CA394187386

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412133G>T (hg19) ; chr16:g.1362132G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362132G>T , CM000678.2:g.1362132G>T	GRCh38
NC_000016.9:g.1412133G>T , CM000678.1:g.1412133G>T	GRCh37
NC_000016.8:g.1352134G>T	NCBI36
NG_016985.1:g.15234G>T
NG_033129.1:g.57573C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.510+1G>T
ENST00000529110.2:c.495+1G>T	ENSP00000435349.2:n.495+1G>T
ENST00000529957.6:n.469+1G>T
ENST00000683366.1:c.*143+1G>T	ENSP00000507283.1:n.*143+1G>T
ENST00000683887.1:c.459+1G>T	ENSP00000506886.1:n.459+1G>T
ENST00000684100.1:n.405+1G>T
ENST00000684126.1:n.469+1G>T
ENST00000684688.1:n.1036+1G>T
ENST00000204679.9:c.411+1G>T MANE Select	ENSP00000204679.4:n.411+1G>T
ENST00000204679.8:c.411+1G>T	ENSP00000204679.4:n.411+1G>T
ENST00000527076.1:n.1427+1G>T
ENST00000527168.5:n.447+1G>T
ENST00000529110.1:c.478+1G>T
ENST00000529957.5:n.510+1G>T
NM_032520.4:c.411+1G>T	NP_115909.1:n.411+1G>T
XM_017023782.1:c.459+1G>T	XP_016879271.1:n.459+1G>T
XM_017023783.1:c.51+1G>T	XP_016879272.1:n.51+1G>T
NM_032520.5:c.411+1G>T MANE Select	NP_115909.1:n.411+1G>T