Canonical Allele Identifier: CA394188635

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412736G>C (hg19) ; chr16:g.1362735G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362735G>C , CM000678.2:g.1362735G>C	GRCh38
NC_000016.9:g.1412736G>C , CM000678.1:g.1412736G>C	GRCh37
NC_000016.8:g.1352737G>C	NCBI36
NG_016985.1:g.15837G>C
NG_033129.1:g.56970C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.833G>C
ENST00000529110.2:c.818G>C	ENSP00000435349.2:p.Cys273Ser
ENST00000529957.6:n.792G>C
ENST00000683366.1:c.*466G>C	ENSP00000507283.1:n.*466G>C
ENST00000683887.1:c.782G>C	ENSP00000506886.1:p.Cys261Ser
ENST00000684100.1:n.728G>C
ENST00000684126.1:n.868G>C
ENST00000684688.1:n.1359G>C
ENST00000204679.9:c.734G>C MANE Select	ENSP00000204679.4:p.Cys245Ser
ENST00000204679.8:c.734G>C	ENSP00000204679.4:p.Cys245Ser
ENST00000527076.1:n.1957G>C
ENST00000527168.5:n.901G>C
ENST00000529957.5:n.833G>C
NM_032520.4:c.734G>C	NP_115909.1:p.Cys245Ser
XM_017023782.1:c.782G>C	XP_016879271.1:p.Cys261Ser
XM_017023783.1:c.374G>C	XP_016879272.1:p.Cys125Ser
NM_032520.5:c.734G>C MANE Select	NP_115909.1:p.Cys245Ser