Canonical Allele Identifier: CA337896738

Gene: CDK11B MMP23B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1655477T>C , CM000663.2:g.1655477T>C	GRCh38
NC_000001.10:g.1586931T>C , CM000663.1:g.1586931T>C	GRCh37
NC_000001.9:g.1576794T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341832.11:c.119A>G (CDK11B) MANE Select	ENSP00000463048.2:p.Asp40Gly
ENST00000340677.9:c.17A>G (CDK11B)	ENSP00000464016.2:p.Asp6Gly
ENST00000341028.8:n.238A>G (CDK11B)
ENST00000341832.10:c.119A>G (CDK11B)	ENSP00000463048.2:p.Asp40Gly
ENST00000407249.7:c.119A>G (CDK11B)	ENSP00000464036.2:p.Asp40Gly
ENST00000412810.6:c.760+21565T>C (MMP23B)	ENSP00000482367.1:n.760+21565T>C
ENST00000611150.3:c.119A>G (CDK11B)	ENSP00000484222.1:p.Asp40Gly
ENST00000615951.4:c.119A>G (CDK11B)	ENSP00000481846.1:p.Asp40Gly
ENST00000618459.4:c.827+21565T>C (MMP23B)	ENSP00000482664.1:n.827+21565T>C
ENST00000626918.2:c.119A>G (CDK11B)	ENSP00000485705.1:p.Asp40Gly
ENST00000629289.2:c.119A>G (CDK11B)	ENSP00000485937.1:p.Asp40Gly
ENST00000629312.2:c.119A>G (CDK11B)	ENSP00000485849.1:p.Asp40Gly
NM_001291345.1:c.119A>G (CDK11B)	NP_001278274.1:p.Asp40Gly
NM_001787.2:c.119A>G (CDK11B)	NP_001778.2:p.Asp40Gly
NM_033486.2:c.119A>G (CDK11B)	NP_277021.2:p.Asp40Gly
NM_033487.2:c.-390A>G (CDK11B)	NP_277022.1:n.-390A>G
NM_033489.2:c.17A>G (CDK11B)	NP_277024.2:p.Asp6Gly
NM_033490.2:c.-396A>G (CDK11B)	NP_277025.1:n.-396A>G
XM_006711065.2:c.119A>G (CDK11B)	XP_006711128.1:p.Asp40Gly
XM_011542490.1:c.119A>G (CDK11B)	XP_011540792.1:p.Asp40Gly
XM_011542491.1:c.119A>G (CDK11B)	XP_011540793.1:p.Asp40Gly
XM_011542492.1:c.119A>G (CDK11B)	XP_011540794.1:p.Asp40Gly
XM_011542493.1:c.119A>G (CDK11B)	XP_011540795.1:p.Asp40Gly
XM_011542494.1:c.17A>G (CDK11B)	XP_011540796.1:p.Asp6Gly
XM_011542495.1:c.17A>G (CDK11B)	XP_011540797.1:p.Asp6Gly
XM_006711065.4:c.119A>G (CDK11B)	XP_006711128.1:p.Asp40Gly
XM_011542490.3:c.119A>G (CDK11B)	XP_011540792.1:p.Asp40Gly
XM_011542491.2:c.119A>G (CDK11B)	XP_011540793.1:p.Asp40Gly
XM_011542492.2:c.119A>G (CDK11B)	XP_011540794.1:p.Asp40Gly
XM_011542493.3:c.119A>G (CDK11B)	XP_011540795.1:p.Asp40Gly
XM_011542494.3:c.17A>G (CDK11B)	XP_011540796.1:p.Asp6Gly
XM_011542495.3:c.17A>G (CDK11B)	XP_011540797.1:p.Asp6Gly
XM_017002925.2:c.119A>G (CDK11B)	XP_016858414.1:p.Asp40Gly
XM_017002926.2:c.119A>G (CDK11B)	XP_016858415.1:p.Asp40Gly
XM_017002927.2:c.17A>G (CDK11B)	XP_016858416.1:p.Asp6Gly
XM_017002928.2:c.17A>G (CDK11B)	XP_016858417.1:p.Asp6Gly
XM_024451174.1:c.17A>G (CDK11B)	XP_024306942.1:p.Asp6Gly
XM_024451190.1:c.-921A>G (CDK11B)	XP_024306958.1:n.-921A>G
XR_002958171.1:n.838A>G (CDK11B)
XR_002958172.1:n.838A>G (CDK11B)
XR_002958173.1:n.838A>G (CDK11B)
XR_002958174.1:n.838A>G (CDK11B)
NM_001291345.2:c.119A>G (CDK11B)	NP_001278274.1:p.Asp40Gly
NM_001787.3:c.119A>G (CDK11B)	NP_001778.2:p.Asp40Gly
NM_033486.3:c.119A>G (CDK11B) MANE Select	NP_277021.2:p.Asp40Gly
NM_033487.3:c.-390A>G (CDK11B)	NP_277022.1:n.-390A>G
NM_033489.3:c.17A>G (CDK11B)	NP_277024.2:p.Asp6Gly
NM_033490.3:c.-396A>G (CDK11B)	NP_277025.1:n.-396A>G