Canonical Allele Identifier: CA1980194805

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521060G= , CM000673.2:g.67521060G=	GRCh38
NC_000011.9:g.67288531G= , CM000673.1:g.67288531G=	GRCh37
NC_000011.8:g.67045107G=	NCBI36
NG_032982.1:g.7369C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.344C= MANE Select	ENSP00000294288.4:p.Thr115=
ENST00000545205.2:c.*129C=	ENSP00000446180.1:n.*129C=
ENST00000636477.1:c.296C=	ENSP00000490746.1:p.Thr99=
ENST00000294288.4:c.344C=	ENSP00000294288.4:p.Thr115=
ENST00000353903.9:c.173C=	ENSP00000312037.4:p.Thr58=
ENST00000545205.1:c.*129C=	ENSP00000446180.1:n.*129C=
NM_016366.2:c.344C=	NP_057450.2:p.Thr115=
XM_005274046.1:c.362C=	XP_005274103.1:p.Thr121=
NM_001318496.1:c.362C=	NP_001305425.1:p.Thr121=
NM_001318496.2:c.362C=	NP_001305425.1:p.Thr121=
NM_016366.3:c.344C= MANE Select	NP_057450.2:p.Thr115=