Canonical Allele Identifier: CA1980194848

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521077G= , CM000673.2:g.67521077G=	GRCh38
NC_000011.9:g.67288548G= , CM000673.1:g.67288548G=	GRCh37
NC_000011.8:g.67045124G=	NCBI36
NG_032982.1:g.7352C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.327C= MANE Select	ENSP00000294288.4:p.Thr109=
ENST00000545205.2:c.*112C=	ENSP00000446180.1:n.*112C=
ENST00000636477.1:c.279C=	ENSP00000490746.1:p.Thr93=
ENST00000294288.4:c.327C=	ENSP00000294288.4:p.Thr109=
ENST00000353903.9:c.156C=	ENSP00000312037.4:p.Thr52=
ENST00000545205.1:c.*112C=	ENSP00000446180.1:n.*112C=
NM_016366.2:c.327C=	NP_057450.2:p.Thr109=
XM_005274046.1:c.345C=	XP_005274103.1:p.Thr115=
NM_001318496.1:c.345C=	NP_001305425.1:p.Thr115=
NM_001318496.2:c.345C=	NP_001305425.1:p.Thr115=
NM_016366.3:c.327C= MANE Select	NP_057450.2:p.Thr109=