Canonical Allele Identifier: CA1980194915

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521103G= , CM000673.2:g.67521103G=	GRCh38
NC_000011.9:g.67288574G= , CM000673.1:g.67288574G=	GRCh37
NC_000011.8:g.67045150G=	NCBI36
NG_032982.1:g.7326C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.301C= MANE Select	ENSP00000294288.4:p.Arg101=
ENST00000545205.2:c.*86C=	ENSP00000446180.1:n.*86C=
ENST00000636477.1:c.253C=	ENSP00000490746.1:p.Arg85=
ENST00000294288.4:c.301C=	ENSP00000294288.4:p.Arg101=
ENST00000353903.9:c.130C=	ENSP00000312037.4:p.Arg44=
ENST00000545205.1:c.*86C=	ENSP00000446180.1:n.*86C=
NM_016366.2:c.301C=	NP_057450.2:p.Arg101=
XM_005274046.1:c.319C=	XP_005274103.1:p.Arg107=
NM_001318496.1:c.319C=	NP_001305425.1:p.Arg107=
NM_001318496.2:c.319C=	NP_001305425.1:p.Arg107=
NM_016366.3:c.301C= MANE Select	NP_057450.2:p.Arg101=