Canonical Allele Identifier: CA2573146909
Community Standard Title: NM_005188.4(CBL):c.1941+10A>C
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119285576A>C , CM000673.2:g.119285576A>C GRCh38
NC_000011.9:g.119156286A>C , CM000673.1:g.119156286A>C GRCh37
NC_000011.8:g.118661496A>C NCBI36
NG_016808.1:g.84297A>C , LRG_608:g.84297A>C

Transcript Alleles

HGVS Amino-acid Change
NM_005188.4:c.1941+10A>C MANE Select NP_005179.2:n.1941+10A>C
ENST00000264033.6:c.1941+10A>C MANE Select ENSP00000264033.3:n.1941+10A>C
NM_005188.3:c.1941+10A>C , LRG_608t1:c.1941+10A>C NP_005179.2:n.1941+10A>C
ENST00000264033.5:c.1941+10A>C ENSP00000264033.3:n.1941+10A>C
ENST00000634586.1:c.1941+10A>C ENSP00000489218.1:n.1941+10A>C
ENST00000634840.1:c.1809+10A>C ENSP00000489324.1:n.1809+10A>C
ENST00000637974.1:c.1935+10A>C ENSP00000490763.1:n.1935+10A>C
ENST00000700472.1:c.*1393+10A>C ENSP00000515005.1:n.*1393+10A>C