Canonical Allele Identifier: CA394186733

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1411875A>C (hg19) ; chr16:g.1361874A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361874A>C , CM000678.2:g.1361874A>C	GRCh38
NC_000016.9:g.1411875A>C , CM000678.1:g.1411875A>C	GRCh37
NC_000016.8:g.1351876A>C	NCBI36
NG_016985.1:g.14976A>C
NG_033129.1:g.57831T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.335A>C
ENST00000529110.2:c.320A>C	ENSP00000435349.2:p.Tyr107Ser
ENST00000529957.6:n.294A>C
ENST00000683366.1:c.181A>C	ENSP00000507283.1:p.Thr61Pro
ENST00000683887.1:c.284A>C	ENSP00000506886.1:p.Tyr95Ser
ENST00000684100.1:n.230A>C
ENST00000684126.1:n.294A>C
ENST00000684688.1:n.861A>C
ENST00000204679.9:c.236A>C MANE Select	ENSP00000204679.4:p.Tyr79Ser
ENST00000204679.8:c.236A>C	ENSP00000204679.4:p.Tyr79Ser
ENST00000526820.5:c.*138A>C	ENSP00000434413.1:n.*138A>C
ENST00000527076.1:n.1252A>C
ENST00000527168.5:n.272A>C
ENST00000529110.1:c.303A>C
ENST00000529957.5:n.335A>C
NM_032520.4:c.236A>C	NP_115909.1:p.Tyr79Ser
XM_017023782.1:c.284A>C	XP_016879271.1:p.Tyr95Ser
XM_017023783.1:c.-125A>C	XP_016879272.1:n.-125A>C
NM_032520.5:c.236A>C MANE Select	NP_115909.1:p.Tyr79Ser