Canonical Allele Identifier: CA394188444

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412645G>T (hg19) ; chr16:g.1362644G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362644G>T , CM000678.2:g.1362644G>T	GRCh38
NC_000016.9:g.1412645G>T , CM000678.1:g.1412645G>T	GRCh37
NC_000016.8:g.1352646G>T	NCBI36
NG_016985.1:g.15746G>T
NG_033129.1:g.57061C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.742G>T
ENST00000529110.2:c.727G>T	ENSP00000435349.2:p.Asp243Tyr
ENST00000529957.6:n.701G>T
ENST00000683366.1:c.*375G>T	ENSP00000507283.1:n.*375G>T
ENST00000683887.1:c.691G>T	ENSP00000506886.1:p.Asp231Tyr
ENST00000684100.1:n.637G>T
ENST00000684126.1:n.777G>T
ENST00000684688.1:n.1268G>T
ENST00000204679.9:c.643G>T MANE Select	ENSP00000204679.4:p.Asp215Tyr
ENST00000204679.8:c.643G>T	ENSP00000204679.4:p.Asp215Tyr
ENST00000527076.1:n.1866G>T
ENST00000527168.5:n.810G>T
ENST00000529957.5:n.742G>T
NM_032520.4:c.643G>T	NP_115909.1:p.Asp215Tyr
XM_017023782.1:c.691G>T	XP_016879271.1:p.Asp231Tyr
XM_017023783.1:c.283G>T	XP_016879272.1:p.Asp95Tyr
NM_032520.5:c.643G>T MANE Select	NP_115909.1:p.Asp215Tyr