Canonical Allele Identifier: CA1980194879

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521088A= , CM000673.2:g.67521088A=	GRCh38
NC_000011.9:g.67288559A= , CM000673.1:g.67288559A=	GRCh37
NC_000011.8:g.67045135A=	NCBI36
NG_032982.1:g.7341T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.316T= MANE Select	ENSP00000294288.4:p.Cys106=
ENST00000545205.2:c.*101T=	ENSP00000446180.1:n.*101T=
ENST00000636477.1:c.268T=	ENSP00000490746.1:p.Cys90=
ENST00000294288.4:c.316T=	ENSP00000294288.4:p.Cys106=
ENST00000353903.9:c.145T=	ENSP00000312037.4:p.Cys49=
ENST00000545205.1:c.*101T=	ENSP00000446180.1:n.*101T=
NM_016366.2:c.316T=	NP_057450.2:p.Cys106=
XM_005274046.1:c.334T=	XP_005274103.1:p.Cys112=
NM_001318496.1:c.334T=	NP_001305425.1:p.Cys112=
NM_001318496.2:c.334T=	NP_001305425.1:p.Cys112=
NM_016366.3:c.316T= MANE Select	NP_057450.2:p.Cys106=