Canonical Allele Identifier: CA395782298

Gene: GPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.46897690G>C , CM000678.2:g.46897690G>C	GRCh38
NC_000016.9:g.46931602G>C , CM000678.1:g.46931602G>C	GRCh37
NC_000016.8:g.45489103G>C	NCBI36
NG_042110.1:g.18311G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340124.9:c.286G>C MANE Select	ENSP00000345282.4:p.Gly96Arg
ENST00000340124.8:c.286G>C	ENSP00000345282.4:p.Gly96Arg
ENST00000440783.2:c.-15G>C	ENSP00000413804.2:n.-15G>C
ENST00000562132.5:c.52G>C	ENSP00000457475.1:p.Gly18Arg
NM_001142466.1:c.-15G>C	NP_001135938.1:n.-15G>C
NM_001142466.2:c.-15G>C	NP_001135938.1:n.-15G>C
NM_133443.2:c.286G>C	NP_597700.1:p.Gly96Arg
NM_133443.3:c.286G>C	NP_597700.1:p.Gly96Arg
NM_133443.4:c.286G>C MANE Select	NP_597700.1:p.Gly96Arg
NM_001142466.3:c.-15G>C	NP_001135938.1:n.-15G>C