Canonical Allele Identifier: CA381519040

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67522683C>T , CM000673.2:g.67522683C>T	GRCh38
NC_000011.9:g.67290154C>T , CM000673.1:g.67290154C>T	GRCh37
NC_000011.8:g.67046730C>T	NCBI36
NG_032982.1:g.5746G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.76G>A MANE Select	ENSP00000294288.4:p.Gly26Ser
ENST00000545205.2:c.76G>A	ENSP00000446180.1:p.Gly26Ser
ENST00000636477.1:c.166-701G>A	ENSP00000490746.1:n.166-701G>A
ENST00000294288.4:c.76G>A	ENSP00000294288.4:p.Gly26Ser
ENST00000353903.9:c.42+602G>A	ENSP00000312037.4:n.42+602G>A
ENST00000545205.1:c.76G>A	ENSP00000446180.1:p.Gly26Ser
NM_016366.2:c.76G>A	NP_057450.2:p.Gly26Ser
XM_005274046.1:c.90G>A	XP_005274103.1:p.Gly30=
NM_001318496.1:c.90G>A	NP_001305425.1:p.Gly30=
NM_001318496.2:c.90G>A	NP_001305425.1:p.Gly30=
NM_016366.3:c.76G>A MANE Select	NP_057450.2:p.Gly26Ser