Canonical Allele Identifier: CA2003905990
Community Standard Title: NM_005188.4(CBL):c.1186T= (p.Cys396=)
Gene: CBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278256T= , CM000673.2:g.119278256T= GRCh38
NC_000011.9:g.119148966T= , CM000673.1:g.119148966T= GRCh37
NC_000011.8:g.118654176T= NCBI36
NG_016808.1:g.76977T= , LRG_608:g.76977T=

Transcript Alleles

HGVS Amino-acid Change
NM_005188.4:c.1186T= MANE Select NP_005179.2:p.Cys396=
ENST00000264033.6:c.1186T= MANE Select ENSP00000264033.3:p.Cys396=
NM_005188.3:c.1186T= , LRG_608t1:c.1186T= NP_005179.2:p.Cys396=
ENST00000264033.5:c.1186T= ENSP00000264033.3:p.Cys396=
ENST00000634586.1:c.1186T= ENSP00000489218.1:p.Cys396=
ENST00000634840.1:c.1186T= ENSP00000489324.1:p.Cys396=
ENST00000637974.1:c.1180T= ENSP00000490763.1:p.Cys394=
ENST00000700472.1:c.*638T= ENSP00000515005.1:n.*638T=
XM_011543057.1:c.1186T= XP_011541359.1:p.Cys396=