Canonical Allele Identifier: CA381513784

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67520052T>G , CM000673.2:g.67520052T>G	GRCh38
NC_000011.9:g.67287523T>G , CM000673.1:g.67287523T>G	GRCh37
NC_000011.8:g.67044099T>G	NCBI36
NG_032982.1:g.8377A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.488A>C MANE Select	ENSP00000294288.4:p.Glu163Ala
ENST00000545205.2:c.*273A>C	ENSP00000446180.1:n.*273A>C
ENST00000636477.1:c.440A>C	ENSP00000490746.1:p.Glu147Ala
ENST00000294288.4:c.488A>C	ENSP00000294288.4:p.Glu163Ala
ENST00000353903.9:c.317A>C	ENSP00000312037.4:p.Glu106Ala
ENST00000545205.1:c.*273A>C	ENSP00000446180.1:n.*273A>C
NM_016366.2:c.488A>C	NP_057450.2:p.Glu163Ala
XM_005274046.1:c.506A>C	XP_005274103.1:p.Glu169Ala
NM_001318496.1:c.506A>C	NP_001305425.1:p.Glu169Ala
NM_001318496.2:c.506A>C	NP_001305425.1:p.Glu169Ala
NM_016366.3:c.488A>C MANE Select	NP_057450.2:p.Glu163Ala