Canonical Allele Identifier: CA2038994716

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750526_57750528delinsCAT , CM000674.2:g.57750526_57750528delinsCAT	GRCh38
NC_000012.11:g.58144309_58144311delinsCAT , CM000674.1:g.58144309_58144311delinsCAT	GRCh37
NC_000012.10:g.56430576_56430578delinsCAT	NCBI36
NG_007484.2:g.6854_6856delinsATG , LRG_490:g.6854_6856delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+128_632+130delinsATG MANE Select	ENSP00000257904.5:n.632+128_632+130delinsATG
ENST00000257904.10:c.632+128_632+130delinsATG	ENSP00000257904.5:n.632+128_632+130delinsATG
ENST00000312990.10:c.280+128_280+130delinsATG	ENSP00000316889.6:n.280+128_280+130delinsATG
ENST00000546489.5:c.410+128_410+130delinsATG	ENSP00000447779.1:n.410+128_410+130delinsATG
ENST00000547281.5:c.410+128_410+130delinsATG	ENSP00000447274.1:n.410+128_410+130delinsATG
ENST00000549606.5:c.-157-1024_-157-1022delinsATG	ENSP00000447005.1:n.-157-1024_-157-1022delinsATG
ENST00000550419.5:c.558_560delinsATG	ENSP00000448098.1:p.Gln186=
ENST00000551888.5:n.458+128_458+130delinsATG
ENST00000553237.5:c.*271+128_*271+130delinsATG	ENSP00000448885.1:n.*271+128_*271+130delinsATG
NM_000075.3:c.632+128_632+130delinsATG	NP_000066.1:n.632+128_632+130delinsATG
NM_000075.4:c.632+128_632+130delinsATG MANE Select	NP_000066.1:n.632+128_632+130delinsATG