Canonical Allele Identifier: CA229644370
Community Standard Title: NM_005188.4(CBL):c.1942-17T>C
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119287835T>C , CM000673.2:g.119287835T>C GRCh38
NC_000011.9:g.119158545T>C , CM000673.1:g.119158545T>C GRCh37
NC_000011.8:g.118663755T>C NCBI36
NG_016808.1:g.86556T>C , LRG_608:g.86556T>C

Transcript Alleles

HGVS Amino-acid Change
NM_005188.4:c.1942-17T>C MANE Select NP_005179.2:n.1942-17T>C
ENST00000264033.6:c.1942-17T>C MANE Select ENSP00000264033.3:n.1942-17T>C
NM_005188.3:c.1942-17T>C , LRG_608t1:c.1942-17T>C NP_005179.2:n.1942-17T>C
ENST00000264033.5:c.1942-17T>C ENSP00000264033.3:n.1942-17T>C
ENST00000634586.1:c.1942-17T>C ENSP00000489218.1:n.1942-17T>C
ENST00000634840.1:c.1810-17T>C ENSP00000489324.1:n.1810-17T>C
ENST00000637974.1:c.1936-17T>C ENSP00000490763.1:n.1936-17T>C
ENST00000700472.1:c.*1394-17T>C ENSP00000515005.1:n.*1394-17T>C