Canonical Allele Identifier: CA1980194679

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521027A= , CM000673.2:g.67521027A=	GRCh38
NC_000011.9:g.67288498A= , CM000673.1:g.67288498A=	GRCh37
NC_000011.8:g.67045074A=	NCBI36
NG_032982.1:g.7402T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.377T= MANE Select	ENSP00000294288.4:p.Ile126=
ENST00000545205.2:c.*162T=	ENSP00000446180.1:n.*162T=
ENST00000636477.1:c.329T=	ENSP00000490746.1:p.Ile110=
ENST00000294288.4:c.377T=	ENSP00000294288.4:p.Ile126=
ENST00000353903.9:c.206T=	ENSP00000312037.4:p.Ile69=
ENST00000545205.1:c.*162T=	ENSP00000446180.1:n.*162T=
NM_016366.2:c.377T=	NP_057450.2:p.Ile126=
XM_005274046.1:c.395T=	XP_005274103.1:p.Ile132=
NM_001318496.1:c.395T=	NP_001305425.1:p.Ile132=
NM_001318496.2:c.395T=	NP_001305425.1:p.Ile132=
NM_016366.3:c.377T= MANE Select	NP_057450.2:p.Ile126=