Canonical Allele Identifier: CA1980194729

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521044G= , CM000673.2:g.67521044G=	GRCh38
NC_000011.9:g.67288515G= , CM000673.1:g.67288515G=	GRCh37
NC_000011.8:g.67045091G=	NCBI36
NG_032982.1:g.7385C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.360C= MANE Select	ENSP00000294288.4:p.Ile120=
ENST00000545205.2:c.*145C=	ENSP00000446180.1:n.*145C=
ENST00000636477.1:c.312C=	ENSP00000490746.1:p.Ile104=
ENST00000294288.4:c.360C=	ENSP00000294288.4:p.Ile120=
ENST00000353903.9:c.189C=	ENSP00000312037.4:p.Ile63=
ENST00000545205.1:c.*145C=	ENSP00000446180.1:n.*145C=
NM_016366.2:c.360C=	NP_057450.2:p.Ile120=
XM_005274046.1:c.378C=	XP_005274103.1:p.Ile126=
NM_001318496.1:c.378C=	NP_001305425.1:p.Ile126=
NM_001318496.2:c.378C=	NP_001305425.1:p.Ile126=
NM_016366.3:c.360C= MANE Select	NP_057450.2:p.Ile120=