Canonical Allele Identifier: CA2220108783

Gene: GPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.46922414C= , CM000678.2:g.46922414C=	GRCh38
NC_000016.9:g.46956326C= , CM000678.1:g.46956326C=	GRCh37
NC_000016.8:g.45513827C=	NCBI36
NG_042110.1:g.43035C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340124.9:c.1210C= MANE Select	ENSP00000345282.4:p.Arg404=
ENST00000340124.8:c.1210C=	ENSP00000345282.4:p.Arg404=
ENST00000440783.2:c.910C=	ENSP00000413804.2:p.Arg304=
ENST00000562801.5:n.1720C=
NM_001142466.1:c.910C=	NP_001135938.1:p.Arg304=
NM_001142466.2:c.910C=	NP_001135938.1:p.Arg304=
NM_133443.2:c.1210C=	NP_597700.1:p.Arg404=
NM_133443.3:c.1210C=	NP_597700.1:p.Arg404=
XM_017023790.1:c.778C=	XP_016879279.1:p.Arg260=
NM_133443.4:c.1210C= MANE Select	NP_597700.1:p.Arg404=
NM_001142466.3:c.910C=	NP_001135938.1:p.Arg304=