Canonical Allele Identifier: CA1980194664

Gene: CABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521021A= , CM000673.2:g.67521021A=	GRCh38
NC_000011.9:g.67288492A= , CM000673.1:g.67288492A=	GRCh37
NC_000011.8:g.67045068A=	NCBI36
NG_032982.1:g.7408T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.379+4T= MANE Select	ENSP00000294288.4:n.379+4T=
ENST00000545205.2:c.*164+4T=	ENSP00000446180.1:n.*164+4T=
ENST00000636477.1:c.331+4T=	ENSP00000490746.1:n.331+4T=
ENST00000294288.4:c.379+4T=	ENSP00000294288.4:n.379+4T=
ENST00000353903.9:c.208+4T=	ENSP00000312037.4:n.208+4T=
ENST00000545205.1:c.*164+4T=	ENSP00000446180.1:n.*164+4T=
NM_016366.2:c.379+4T=	NP_057450.2:n.379+4T=
XM_005274046.1:c.397+4T=	XP_005274103.1:n.397+4T=
NM_001318496.1:c.397+4T=	NP_001305425.1:n.397+4T=
NM_001318496.2:c.397+4T=	NP_001305425.1:n.397+4T=
NM_016366.3:c.379+4T= MANE Select	NP_057450.2:n.379+4T=