Canonical Allele Identifier: CA6142494

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521059G>T , CM000673.2:g.67521059G>T	GRCh38
NC_000011.9:g.67288530G>T , CM000673.1:g.67288530G>T	GRCh37
NC_000011.8:g.67045106G>T	NCBI36
NG_032982.1:g.7370C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.345C>A MANE Select	ENSP00000294288.4:p.Thr115=
ENST00000545205.2:c.*130C>A	ENSP00000446180.1:n.*130C>A
ENST00000636477.1:c.297C>A	ENSP00000490746.1:p.Thr99=
ENST00000294288.4:c.345C>A	ENSP00000294288.4:p.Thr115=
ENST00000353903.9:c.174C>A	ENSP00000312037.4:p.Thr58=
ENST00000545205.1:c.*130C>A	ENSP00000446180.1:n.*130C>A
NM_016366.2:c.345C>A	NP_057450.2:p.Thr115=
XM_005274046.1:c.363C>A	XP_005274103.1:p.Thr121=
NM_001318496.1:c.363C>A	NP_001305425.1:p.Thr121=
NM_001318496.2:c.363C>A	NP_001305425.1:p.Thr121=
NM_016366.3:c.345C>A MANE Select	NP_057450.2:p.Thr115=