Canonical Allele Identifier: CA381515274

Gene: CABP2

Linked Data

• MyVariant Identifiers: chr11:g.67288502G>T (hg19) ; chr11:g.67521031G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521031G>T , CM000673.2:g.67521031G>T	GRCh38
NC_000011.9:g.67288502G>T , CM000673.1:g.67288502G>T	GRCh37
NC_000011.8:g.67045078G>T	NCBI36
NG_032982.1:g.7398C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.373C>A MANE Select	ENSP00000294288.4:p.Gln125Lys
ENST00000545205.2:c.*158C>A	ENSP00000446180.1:n.*158C>A
ENST00000636477.1:c.325C>A	ENSP00000490746.1:p.Gln109Lys
ENST00000294288.4:c.373C>A	ENSP00000294288.4:p.Gln125Lys
ENST00000353903.9:c.202C>A	ENSP00000312037.4:p.Gln68Lys
ENST00000545205.1:c.*158C>A	ENSP00000446180.1:n.*158C>A
NM_016366.2:c.373C>A	NP_057450.2:p.Gln125Lys
XM_005274046.1:c.391C>A	XP_005274103.1:p.Gln131Lys
NM_001318496.1:c.391C>A	NP_001305425.1:p.Gln131Lys
NM_001318496.2:c.391C>A	NP_001305425.1:p.Gln131Lys
NM_016366.3:c.373C>A MANE Select	NP_057450.2:p.Gln125Lys