Canonical Allele Identifier: CA381515347

Gene: CABP2

Linked Data

• MyVariant Identifiers: chr11:g.67288513T>A (hg19) ; chr11:g.67521042T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521042T>A , CM000673.2:g.67521042T>A	GRCh38
NC_000011.9:g.67288513T>A , CM000673.1:g.67288513T>A	GRCh37
NC_000011.8:g.67045089T>A	NCBI36
NG_032982.1:g.7387A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.362A>T MANE Select	ENSP00000294288.4:p.Glu121Val
ENST00000545205.2:c.*147A>T	ENSP00000446180.1:n.*147A>T
ENST00000636477.1:c.314A>T	ENSP00000490746.1:p.Glu105Val
ENST00000294288.4:c.362A>T	ENSP00000294288.4:p.Glu121Val
ENST00000353903.9:c.191A>T	ENSP00000312037.4:p.Glu64Val
ENST00000545205.1:c.*147A>T	ENSP00000446180.1:n.*147A>T
NM_016366.2:c.362A>T	NP_057450.2:p.Glu121Val
XM_005274046.1:c.380A>T	XP_005274103.1:p.Glu127Val
NM_001318496.1:c.380A>T	NP_001305425.1:p.Glu127Val
NM_001318496.2:c.380A>T	NP_001305425.1:p.Glu127Val
NM_016366.3:c.362A>T MANE Select	NP_057450.2:p.Glu121Val