Canonical Allele Identifier: CA394187830

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412265G>C (hg19) ; chr16:g.1362264G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362264G>C , CM000678.2:g.1362264G>C	GRCh38
NC_000016.9:g.1412265G>C , CM000678.1:g.1412265G>C	GRCh37
NC_000016.8:g.1352266G>C	NCBI36
NG_016985.1:g.15366G>C
NG_033129.1:g.57441C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.569G>C
ENST00000529110.2:c.554G>C	ENSP00000435349.2:p.Cys185Ser
ENST00000529957.6:n.528G>C
ENST00000683366.1:c.*202G>C	ENSP00000507283.1:n.*202G>C
ENST00000683887.1:c.518G>C	ENSP00000506886.1:p.Cys173Ser
ENST00000684100.1:n.464G>C
ENST00000684126.1:n.528G>C
ENST00000684688.1:n.1095G>C
ENST00000204679.9:c.470G>C MANE Select	ENSP00000204679.4:p.Cys157Ser
ENST00000204679.8:c.470G>C	ENSP00000204679.4:p.Cys157Ser
ENST00000527076.1:n.1486G>C
ENST00000527168.5:n.506G>C
ENST00000529110.1:c.537G>C
ENST00000529957.5:n.569G>C
NM_032520.4:c.470G>C	NP_115909.1:p.Cys157Ser
XM_017023782.1:c.518G>C	XP_016879271.1:p.Cys173Ser
XM_017023783.1:c.110G>C	XP_016879272.1:p.Cys37Ser
NM_032520.5:c.470G>C MANE Select	NP_115909.1:p.Cys157Ser