Canonical Allele Identifier: CA224145832
Gene: CABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67522699G>A , CM000673.2:g.67522699G>A GRCh38
NC_000011.9:g.67290170G>A , CM000673.1:g.67290170G>A GRCh37
NC_000011.8:g.67046746G>A NCBI36
NG_032982.1:g.5730C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000294288.5:c.60C>T MANE Select ENSP00000294288.4:p.Leu20=
ENST00000545205.2:c.60C>T ENSP00000446180.1:p.Leu20=
ENST00000636477.1:c.166-717C>T ENSP00000490746.1:n.166-717C>T
ENST00000294288.4:c.60C>T ENSP00000294288.4:p.Leu20=
ENST00000353903.9:c.42+586C>T ENSP00000312037.4:n.42+586C>T
ENST00000545205.1:c.60C>T ENSP00000446180.1:p.Leu20=
NM_016366.2:c.60C>T NP_057450.2:p.Leu20=
XM_005274046.1:c.74C>T XP_005274103.1:p.Ser25Leu
NM_001318496.1:c.74C>T NP_001305425.1:p.Ser25Leu
NM_001318496.2:c.74C>T NP_001305425.1:p.Ser25Leu
NM_016366.3:c.60C>T MANE Select NP_057450.2:p.Leu20=