Canonical Allele Identifier: CA394187842

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412268T>A (hg19) ; chr16:g.1362267T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362267T>A , CM000678.2:g.1362267T>A	GRCh38
NC_000016.9:g.1412268T>A , CM000678.1:g.1412268T>A	GRCh37
NC_000016.8:g.1352269T>A	NCBI36
NG_016985.1:g.15369T>A
NG_033129.1:g.57438A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.572T>A
ENST00000529110.2:c.557T>A	ENSP00000435349.2:p.Val186Asp
ENST00000529957.6:n.531T>A
ENST00000683366.1:c.*205T>A	ENSP00000507283.1:n.*205T>A
ENST00000683887.1:c.521T>A	ENSP00000506886.1:p.Val174Asp
ENST00000684100.1:n.467T>A
ENST00000684126.1:n.531T>A
ENST00000684688.1:n.1098T>A
ENST00000204679.9:c.473T>A MANE Select	ENSP00000204679.4:p.Val158Asp
ENST00000204679.8:c.473T>A	ENSP00000204679.4:p.Val158Asp
ENST00000527076.1:n.1489T>A
ENST00000527168.5:n.509T>A
ENST00000529110.1:c.540T>A
ENST00000529957.5:n.572T>A
NM_032520.4:c.473T>A	NP_115909.1:p.Val158Asp
XM_017023782.1:c.521T>A	XP_016879271.1:p.Val174Asp
XM_017023783.1:c.113T>A	XP_016879272.1:p.Val38Asp
NM_032520.5:c.473T>A MANE Select	NP_115909.1:p.Val158Asp