Canonical Allele Identifier: CA394186837

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1411895T>C (hg19) ; chr16:g.1361894T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361894T>C , CM000678.2:g.1361894T>C	GRCh38
NC_000016.9:g.1411895T>C , CM000678.1:g.1411895T>C	GRCh37
NC_000016.8:g.1351896T>C	NCBI36
NG_016985.1:g.14996T>C
NG_033129.1:g.57811A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.355T>C
ENST00000529110.2:c.340T>C	ENSP00000435349.2:p.Phe114Leu
ENST00000529957.6:n.314T>C
ENST00000683366.1:c.201T>C	ENSP00000507283.1:p.Arg67=
ENST00000683887.1:c.304T>C	ENSP00000506886.1:p.Phe102Leu
ENST00000684100.1:n.250T>C
ENST00000684126.1:n.314T>C
ENST00000684688.1:n.881T>C
ENST00000204679.9:c.256T>C MANE Select	ENSP00000204679.4:p.Phe86Leu
ENST00000204679.8:c.256T>C	ENSP00000204679.4:p.Phe86Leu
ENST00000526820.5:c.*158T>C	ENSP00000434413.1:n.*158T>C
ENST00000527076.1:n.1272T>C
ENST00000527168.5:n.292T>C
ENST00000529110.1:c.323T>C
ENST00000529957.5:n.355T>C
NM_032520.4:c.256T>C	NP_115909.1:p.Phe86Leu
XM_017023782.1:c.304T>C	XP_016879271.1:p.Phe102Leu
XM_017023783.1:c.-105T>C	XP_016879272.1:n.-105T>C
NM_032520.5:c.256T>C MANE Select	NP_115909.1:p.Phe86Leu