Canonical Allele Identifier: CA1140271281
Gene: MCL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150578851G= , CM000663.2:g.150578851G= GRCh38
NC_000001.10:g.150551327G= , CM000663.1:g.150551327G= GRCh37
NC_000001.9:g.148817951G= NCBI36
NG_029146.1:g.5888C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369026.3:c.680C= MANE Select ENSP00000358022.2:p.Ala227=
ENST00000464132.2:n.627C=
ENST00000676522.1:n.744C=
ENST00000678610.1:c.86C= ENSP00000503149.1:p.Ala29=
ENST00000678770.1:c.680C= ENSP00000502859.1:p.Ala227=
ENST00000307940.3:c.680C= ENSP00000309973.3:p.Ala227=
ENST00000369026.2:c.680C= ENSP00000358022.2:p.Ala227=
ENST00000620947.4:c.221C= ENSP00000477624.1:p.Ala74=
NM_001197320.1:c.221C= NP_001184249.1:p.Ala74=
NM_021960.4:c.680C= NP_068779.1:p.Ala227=
NM_182763.2:c.680C= NP_877495.1:p.Ala227=
NM_021960.5:c.680C= MANE Select NP_068779.1:p.Ala227=
NM_001197320.2:c.221C= NP_001184249.1:p.Ala74=
NM_182763.3:c.680C= NP_877495.1:p.Ala227=