Canonical Allele Identifier: CA2003905425
Gene: CBL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119277883C= , CM000673.2:g.119277883C= GRCh38
NC_000011.9:g.119148593C= , CM000673.1:g.119148593C= GRCh37
NC_000011.8:g.118653803C= NCBI36
NG_016808.1:g.76604C= , LRG_608:g.76604C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*547+39C= ENSP00000515005.1:n.*547+39C=
ENST00000264033.6:c.1095+39C= MANE Select ENSP00000264033.3:n.1095+39C=
ENST00000637974.1:c.1089+39C= ENSP00000490763.1:n.1089+39C=
ENST00000264033.5:c.1095+39C= ENSP00000264033.3:n.1095+39C=
ENST00000634586.1:c.1095+39C= ENSP00000489218.1:n.1095+39C=
ENST00000634840.1:c.1095+39C= ENSP00000489324.1:n.1095+39C=
NM_005188.3:c.1095+39C= , LRG_608t1:c.1095+39C= NP_005179.2:n.1095+39C=
XM_011543057.1:c.1095+39C= XP_011541359.1:n.1095+39C=
NM_005188.4:c.1095+39C= MANE Select NP_005179.2:n.1095+39C=
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