Canonical Allele Identifier: CA2038996897

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751358_57751374delinsGCTCACTTTTCAATCCC , CM000674.2:g.57751358_57751374delinsGCTCACTTTTCAATCCC	GRCh38
NC_000012.11:g.58145141_58145157delinsGCTCACTTTTCAATCCC , CM000674.1:g.58145141_58145157delinsGCTCACTTTTCAATCCC	GRCh37
NC_000012.10:g.56431408_56431424delinsGCTCACTTTTCAATCCC	NCBI36
NG_007484.2:g.6008_6024delinsGGGATTGAAAAGTGAGC , LRG_490:g.6008_6024delinsGGGATTGAAAAGTGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.219-32_219-16delinsGGGATTGAAAAGTGAGC MANE Select	ENSP00000257904.5:n.219-32_219-16delinsGGGATTGAAAAGTGAGC
ENST00000257904.10:c.219-32_219-16delinsGGGATTGAAAAGTGAGC	ENSP00000257904.5:n.219-32_219-16delinsGGGATTGAAAAGTGAGC
ENST00000312990.10:c.219-32_219-16delinsGGGATTGAAAAGTGAGC	ENSP00000316889.6:n.219-32_219-16delinsGGGATTGAAAAGTGAGC
ENST00000546489.5:c.-4-32_-4-16delinsGGGATTGAAAAGTGAGC	ENSP00000447779.1:n.-4-32_-4-16delinsGGGATTGAAAAGTGAGC
ENST00000547281.5:c.-4-32_-4-16delinsGGGATTGAAAAGTGAGC	ENSP00000447274.1:n.-4-32_-4-16delinsGGGATTGAAAAGTGAGC
ENST00000549606.5:c.-158+801_-158+817delinsGGGATTGAAAAGTGAGC	ENSP00000447005.1:n.-158+801_-158+817delinsGGGATTGAAAAGTGAGC
ENST00000550419.5:c.219-32_219-16delinsGGGATTGAAAAGTGAGC	ENSP00000448098.1:n.219-32_219-16delinsGGGATTGAAAAGTGAGC
ENST00000551706.1:n.553_569delinsGGGATTGAAAAGTGAGC
ENST00000551800.5:c.-4-32_-4-16delinsGGGATTGAAAAGTGAGC	ENSP00000449391.1:n.-4-32_-4-16delinsGGGATTGAAAAGTGAGC
ENST00000551888.5:n.397-32_397-16delinsGGGATTGAAAAGTGAGC
ENST00000552254.5:c.219-32_219-16delinsGGGATTGAAAAGTGAGC	ENSP00000449179.1:n.219-32_219-16delinsGGGATTGAAAAGTGAGC
ENST00000552388.1:c.219-32_219-16delinsGGGATTGAAAAGTGAGC	ENSP00000448963.1:n.219-32_219-16delinsGGGATTGAAAAGTGAGC
ENST00000552862.1:c.219-32_219-16delinsGGGATTGAAAAGTGAGC	ENSP00000446763.1:n.219-32_219-16delinsGGGATTGAAAAGTGAGC
ENST00000553237.5:c.218+126_218+142delinsGGGATTGAAAAGTGAGC	ENSP00000448885.1:n.218+126_218+142delinsGGGATTGAAAAGTGAGC
NM_000075.3:c.219-32_219-16delinsGGGATTGAAAAGTGAGC	NP_000066.1:n.219-32_219-16delinsGGGATTGAAAAGTGAGC
NM_000075.4:c.219-32_219-16delinsGGGATTGAAAAGTGAGC MANE Select	NP_000066.1:n.219-32_219-16delinsGGGATTGAAAAGTGAGC