Canonical Allele Identifier: CA394187583

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412208T>C (hg19) ; chr16:g.1362207T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362207T>C , CM000678.2:g.1362207T>C	GRCh38
NC_000016.9:g.1412208T>C , CM000678.1:g.1412208T>C	GRCh37
NC_000016.8:g.1352209T>C	NCBI36
NG_016985.1:g.15309T>C
NG_033129.1:g.57498A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.512T>C
ENST00000529110.2:c.497T>C	ENSP00000435349.2:p.Val166Ala
ENST00000529957.6:n.471T>C
ENST00000683366.1:c.*145T>C	ENSP00000507283.1:n.*145T>C
ENST00000683887.1:c.461T>C	ENSP00000506886.1:p.Val154Ala
ENST00000684100.1:n.407T>C
ENST00000684126.1:n.471T>C
ENST00000684688.1:n.1038T>C
ENST00000204679.9:c.413T>C MANE Select	ENSP00000204679.4:p.Val138Ala
ENST00000204679.8:c.413T>C	ENSP00000204679.4:p.Val138Ala
ENST00000527076.1:n.1429T>C
ENST00000527168.5:n.449T>C
ENST00000529110.1:c.480T>C
ENST00000529957.5:n.512T>C
NM_032520.4:c.413T>C	NP_115909.1:p.Val138Ala
XM_017023782.1:c.461T>C	XP_016879271.1:p.Val154Ala
XM_017023783.1:c.53T>C	XP_016879272.1:p.Val18Ala
NM_032520.5:c.413T>C MANE Select	NP_115909.1:p.Val138Ala