Canonical Allele Identifier: CA382912715
Community Standard Title: NM_005188.4(CBL):c.1186T>A (p.Cys396Ser)
Gene: CBL HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_005188.4:c.1186T>A MANE Select NP_005179.2:p.Cys396Ser
ENST00000264033.6:c.1186T>A MANE Select ENSP00000264033.3:p.Cys396Ser
NM_005188.3:c.1186T>A , LRG_608t1:c.1186T>A NP_005179.2:p.Cys396Ser
ENST00000264033.5:c.1186T>A ENSP00000264033.3:p.Cys396Ser
ENST00000634586.1:c.1186T>A ENSP00000489218.1:p.Cys396Ser
ENST00000634840.1:c.1186T>A ENSP00000489324.1:p.Cys396Ser
ENST00000637974.1:c.1180T>A ENSP00000490763.1:p.Cys394Ser
ENST00000700472.1:c.*638T>A ENSP00000515005.1:n.*638T>A
XM_011543057.1:c.1186T>A XP_011541359.1:p.Cys396Ser