Canonical Allele Identifier: CA381515287

Gene: CABP2

Linked Data

• MyVariant Identifiers: chr11:g.67288504T>G (hg19) ; chr11:g.67521033T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67521033T>G , CM000673.2:g.67521033T>G	GRCh38
NC_000011.9:g.67288504T>G , CM000673.1:g.67288504T>G	GRCh37
NC_000011.8:g.67045080T>G	NCBI36
NG_032982.1:g.7396A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294288.5:c.371A>C MANE Select	ENSP00000294288.4:p.Gln124Pro
ENST00000545205.2:c.*156A>C	ENSP00000446180.1:n.*156A>C
ENST00000636477.1:c.323A>C	ENSP00000490746.1:p.Gln108Pro
ENST00000294288.4:c.371A>C	ENSP00000294288.4:p.Gln124Pro
ENST00000353903.9:c.200A>C	ENSP00000312037.4:p.Gln67Pro
ENST00000545205.1:c.*156A>C	ENSP00000446180.1:n.*156A>C
NM_016366.2:c.371A>C	NP_057450.2:p.Gln124Pro
XM_005274046.1:c.389A>C	XP_005274103.1:p.Gln130Pro
NM_001318496.1:c.389A>C	NP_001305425.1:p.Gln130Pro
NM_001318496.2:c.389A>C	NP_001305425.1:p.Gln130Pro
NM_016366.3:c.371A>C MANE Select	NP_057450.2:p.Gln124Pro