Canonical Allele Identifier: CA3185910159

Gene: CBL MCAM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119310604T= , CM000673.2:g.119310604T=	GRCh38
NC_000011.9:g.119181314T= , CM000673.1:g.119181314T=	GRCh37
NC_000011.8:g.118686524T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006500.3:c.1794-138A= (MCAM) MANE Select	NP_006491.2:n.1794-138A=
ENST00000264036.6:c.1794-138A= (MCAM) MANE Select	ENSP00000264036.4:n.1794-138A=
NM_006500.2:c.1794-138A= (MCAM)	NP_006491.2:n.1794-138A=
ENST00000264036.5:c.1794-138A= (MCAM)	ENSP00000264036.4:n.1794-138A=
ENST00000524940.5:n.177+152A= (MCAM)
ENST00000525586.5:n.3935-138A= (MCAM)
ENST00000528533.5:n.2103-138A= (MCAM)
ENST00000528976.1:n.347-138A= (MCAM)
ENST00000637974.1:c.2522-2814T= (CBL)	ENSP00000490763.1:n.2522-2814T=
ENST00000700472.1:c.*1980-2814T= (CBL)	ENSP00000515005.1:n.*1980-2814T=
XM_017017759.2:c.1731-138A= (MCAM)	XP_016873248.1:n.1731-138A=
XM_017017760.2:c.1698-138A= (MCAM)	XP_016873249.1:n.1698-138A=
XM_017017761.2:c.1793+152A= (MCAM)	XP_016873250.1:n.1793+152A=
XM_017017762.2:c.1730+152A= (MCAM)	XP_016873251.1:n.1730+152A=