Canonical Allele Identifier: CA2220108791
Gene: GPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46922415G= , CM000678.2:g.46922415G= GRCh38
NC_000016.9:g.46956327G= , CM000678.1:g.46956327G= GRCh37
NC_000016.8:g.45513828G= NCBI36
NG_042110.1:g.43036G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340124.9:c.1211G= MANE Select ENSP00000345282.4:p.Arg404=
ENST00000340124.8:c.1211G= ENSP00000345282.4:p.Arg404=
ENST00000440783.2:c.911G= ENSP00000413804.2:p.Arg304=
ENST00000562801.5:n.1721G=
NM_001142466.1:c.911G= NP_001135938.1:p.Arg304=
NM_001142466.2:c.911G= NP_001135938.1:p.Arg304=
NM_133443.2:c.1211G= NP_597700.1:p.Arg404=
NM_133443.3:c.1211G= NP_597700.1:p.Arg404=
XM_017023790.1:c.779G= XP_016879279.1:p.Arg260=
NM_133443.4:c.1211G= MANE Select NP_597700.1:p.Arg404=
NM_001142466.3:c.911G= NP_001135938.1:p.Arg304=