Canonical Allele Identifier: CA395782684

Gene: GPT2

Linked Data

• MyVariant Identifiers: chr16:g.46940768A>C (hg19) ; chr16:g.46906856A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.46906856A>C , CM000678.2:g.46906856A>C	GRCh38
NC_000016.9:g.46940768A>C , CM000678.1:g.46940768A>C	GRCh37
NC_000016.8:g.45498269A>C	NCBI36
NG_042110.1:g.27477A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340124.9:c.457A>C MANE Select	ENSP00000345282.4:p.Ser153Arg
ENST00000340124.8:c.457A>C	ENSP00000345282.4:p.Ser153Arg
ENST00000440783.2:c.157A>C	ENSP00000413804.2:p.Ser53Arg
ENST00000562132.5:c.223A>C	ENSP00000457475.1:p.Ser75Arg
NM_001142466.1:c.157A>C	NP_001135938.1:p.Ser53Arg
NM_001142466.2:c.157A>C	NP_001135938.1:p.Ser53Arg
NM_133443.2:c.457A>C	NP_597700.1:p.Ser153Arg
NM_133443.3:c.457A>C	NP_597700.1:p.Ser153Arg
XM_017023790.1:c.25A>C	XP_016879279.1:p.Ser9Arg
NM_133443.4:c.457A>C MANE Select	NP_597700.1:p.Ser153Arg
NM_001142466.3:c.157A>C	NP_001135938.1:p.Ser53Arg