Canonical Allele Identifier: CA3185910184

Gene: CBL MCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119310948T= , CM000673.2:g.119310948T=	GRCh38
NC_000011.9:g.119181658T= , CM000673.1:g.119181658T=	GRCh37
NC_000011.8:g.118686868T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006500.3:c.1646-45A= (MCAM) MANE Select	NP_006491.2:n.1646-45A=
ENST00000264036.6:c.1646-45A= (MCAM) MANE Select	ENSP00000264036.4:n.1646-45A=
NM_006500.2:c.1646-45A= (MCAM)	NP_006491.2:n.1646-45A=
ENST00000264036.5:c.1646-45A= (MCAM)	ENSP00000264036.4:n.1646-45A=
ENST00000524940.5:n.30-45A= (MCAM)
ENST00000525586.5:n.3742A= (MCAM)
ENST00000528533.5:n.1910A= (MCAM)
ENST00000528976.1:n.199-45A= (MCAM)
ENST00000637974.1:c.2522-2470T= (CBL)	ENSP00000490763.1:n.2522-2470T=
ENST00000700472.1:c.*1980-2470T= (CBL)	ENSP00000515005.1:n.*1980-2470T=
XM_017017759.2:c.1583-45A= (MCAM)	XP_016873248.1:n.1583-45A=
XM_017017760.2:c.1550-45A= (MCAM)	XP_016873249.1:n.1550-45A=
XM_017017761.2:c.1646-45A= (MCAM)	XP_016873250.1:n.1646-45A=
XM_017017762.2:c.1583-45A= (MCAM)	XP_016873251.1:n.1583-45A=