Canonical Allele Identifier: CA394188433

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412640T>A (hg19) ; chr16:g.1362639T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362639T>A , CM000678.2:g.1362639T>A	GRCh38
NC_000016.9:g.1412640T>A , CM000678.1:g.1412640T>A	GRCh37
NC_000016.8:g.1352641T>A	NCBI36
NG_016985.1:g.15741T>A
NG_033129.1:g.57066A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.737T>A
ENST00000529110.2:c.722T>A	ENSP00000435349.2:p.Phe241Tyr
ENST00000529957.6:n.696T>A
ENST00000683366.1:c.*370T>A	ENSP00000507283.1:n.*370T>A
ENST00000683887.1:c.686T>A	ENSP00000506886.1:p.Phe229Tyr
ENST00000684100.1:n.632T>A
ENST00000684126.1:n.772T>A
ENST00000684688.1:n.1263T>A
ENST00000204679.9:c.638T>A MANE Select	ENSP00000204679.4:p.Phe213Tyr
ENST00000204679.8:c.638T>A	ENSP00000204679.4:p.Phe213Tyr
ENST00000527076.1:n.1861T>A
ENST00000527168.5:n.805T>A
ENST00000529957.5:n.737T>A
NM_032520.4:c.638T>A	NP_115909.1:p.Phe213Tyr
XM_017023782.1:c.686T>A	XP_016879271.1:p.Phe229Tyr
XM_017023783.1:c.278T>A	XP_016879272.1:p.Phe93Tyr
NM_032520.5:c.638T>A MANE Select	NP_115909.1:p.Phe213Tyr