Canonical Allele Identifier: CA394187757

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412247T>C (hg19) ; chr16:g.1362246T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362246T>C , CM000678.2:g.1362246T>C	GRCh38
NC_000016.9:g.1412247T>C , CM000678.1:g.1412247T>C	GRCh37
NC_000016.8:g.1352248T>C	NCBI36
NG_016985.1:g.15348T>C
NG_033129.1:g.57459A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.551T>C
ENST00000529110.2:c.536T>C	ENSP00000435349.2:p.Val179Ala
ENST00000529957.6:n.510T>C
ENST00000683366.1:c.*184T>C	ENSP00000507283.1:n.*184T>C
ENST00000683887.1:c.500T>C	ENSP00000506886.1:p.Val167Ala
ENST00000684100.1:n.446T>C
ENST00000684126.1:n.510T>C
ENST00000684688.1:n.1077T>C
ENST00000204679.9:c.452T>C MANE Select	ENSP00000204679.4:p.Val151Ala
ENST00000204679.8:c.452T>C	ENSP00000204679.4:p.Val151Ala
ENST00000527076.1:n.1468T>C
ENST00000527168.5:n.488T>C
ENST00000529110.1:c.519T>C
ENST00000529957.5:n.551T>C
NM_032520.4:c.452T>C	NP_115909.1:p.Val151Ala
XM_017023782.1:c.500T>C	XP_016879271.1:p.Val167Ala
XM_017023783.1:c.92T>C	XP_016879272.1:p.Val31Ala
NM_032520.5:c.452T>C MANE Select	NP_115909.1:p.Val151Ala