Canonical Allele Identifier: CA1980194695

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521032T= , CM000673.2:g.67521032T=	GRCh38
NC_000011.9:g.67288503T= , CM000673.1:g.67288503T=	GRCh37
NC_000011.8:g.67045079T=	NCBI36
NG_032982.1:g.7397A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.372A= MANE Select	ENSP00000294288.4:p.Gln124=
ENST00000545205.2:c.*157A=	ENSP00000446180.1:n.*157A=
ENST00000636477.1:c.324A=	ENSP00000490746.1:p.Gln108=
ENST00000294288.4:c.372A=	ENSP00000294288.4:p.Gln124=
ENST00000353903.9:c.201A=	ENSP00000312037.4:p.Gln67=
ENST00000545205.1:c.*157A=	ENSP00000446180.1:n.*157A=
NM_016366.2:c.372A=	NP_057450.2:p.Gln124=
XM_005274046.1:c.390A=	XP_005274103.1:p.Gln130=
NM_001318496.1:c.390A=	NP_001305425.1:p.Gln130=
NM_001318496.2:c.390A=	NP_001305425.1:p.Gln130=
NM_016366.3:c.372A= MANE Select	NP_057450.2:p.Gln124=