Canonical Allele Identifier: CA1980194842
Gene: CABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67521076G= , CM000673.2:g.67521076G= GRCh38
NC_000011.9:g.67288547G= , CM000673.1:g.67288547G= GRCh37
NC_000011.8:g.67045123G= NCBI36
NG_032982.1:g.7353C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000294288.5:c.328C= MANE Select ENSP00000294288.4:p.Leu110=
ENST00000545205.2:c.*113C= ENSP00000446180.1:n.*113C=
ENST00000636477.1:c.280C= ENSP00000490746.1:p.Leu94=
ENST00000294288.4:c.328C= ENSP00000294288.4:p.Leu110=
ENST00000353903.9:c.157C= ENSP00000312037.4:p.Leu53=
ENST00000545205.1:c.*113C= ENSP00000446180.1:n.*113C=
NM_016366.2:c.328C= NP_057450.2:p.Leu110=
XM_005274046.1:c.346C= XP_005274103.1:p.Leu116=
NM_001318496.1:c.346C= NP_001305425.1:p.Leu116=
NM_001318496.2:c.346C= NP_001305425.1:p.Leu116=
NM_016366.3:c.328C= MANE Select NP_057450.2:p.Leu110=