Canonical Allele Identifier: CA1980194882

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521090G= , CM000673.2:g.67521090G=	GRCh38
NC_000011.9:g.67288561G= , CM000673.1:g.67288561G=	GRCh37
NC_000011.8:g.67045137G=	NCBI36
NG_032982.1:g.7339C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.314C= MANE Select	ENSP00000294288.4:p.Ala105=
ENST00000545205.2:c.*99C=	ENSP00000446180.1:n.*99C=
ENST00000636477.1:c.266C=	ENSP00000490746.1:p.Ala89=
ENST00000294288.4:c.314C=	ENSP00000294288.4:p.Ala105=
ENST00000353903.9:c.143C=	ENSP00000312037.4:p.Ala48=
ENST00000545205.1:c.*99C=	ENSP00000446180.1:n.*99C=
NM_016366.2:c.314C=	NP_057450.2:p.Ala105=
XM_005274046.1:c.332C=	XP_005274103.1:p.Ala111=
NM_001318496.1:c.332C=	NP_001305425.1:p.Ala111=
NM_001318496.2:c.332C=	NP_001305425.1:p.Ala111=
NM_016366.3:c.314C= MANE Select	NP_057450.2:p.Ala105=