Canonical Allele Identifier: CA1980194787

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521058C= , CM000673.2:g.67521058C=	GRCh38
NC_000011.9:g.67288529C= , CM000673.1:g.67288529C=	GRCh37
NC_000011.8:g.67045105C=	NCBI36
NG_032982.1:g.7371G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.346G= MANE Select	ENSP00000294288.4:p.Glu116=
ENST00000545205.2:c.*131G=	ENSP00000446180.1:n.*131G=
ENST00000636477.1:c.298G=	ENSP00000490746.1:p.Glu100=
ENST00000294288.4:c.346G=	ENSP00000294288.4:p.Glu116=
ENST00000353903.9:c.175G=	ENSP00000312037.4:p.Glu59=
ENST00000545205.1:c.*131G=	ENSP00000446180.1:n.*131G=
NM_016366.2:c.346G=	NP_057450.2:p.Glu116=
XM_005274046.1:c.364G=	XP_005274103.1:p.Glu122=
NM_001318496.1:c.364G=	NP_001305425.1:p.Glu122=
NM_001318496.2:c.364G=	NP_001305425.1:p.Glu122=
NM_016366.3:c.346G= MANE Select	NP_057450.2:p.Glu116=