Canonical Allele Identifier: CA2038994794

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750558_57750561delinsCCTG , CM000674.2:g.57750558_57750561delinsCCTG	GRCh38
NC_000012.11:g.58144341_58144344delinsCCTG , CM000674.1:g.58144341_58144344delinsCCTG	GRCh37
NC_000012.10:g.56430608_56430611delinsCCTG	NCBI36
NG_007484.2:g.6821_6824delinsCAGG , LRG_490:g.6821_6824delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+95_632+98delinsCAGG MANE Select	ENSP00000257904.5:n.632+95_632+98delinsCAGG
ENST00000257904.10:c.632+95_632+98delinsCAGG	ENSP00000257904.5:n.632+95_632+98delinsCAGG
ENST00000312990.10:c.280+95_280+98delinsCAGG	ENSP00000316889.6:n.280+95_280+98delinsCAGG
ENST00000546489.5:c.410+95_410+98delinsCAGG	ENSP00000447779.1:n.410+95_410+98delinsCAGG
ENST00000547281.5:c.410+95_410+98delinsCAGG	ENSP00000447274.1:n.410+95_410+98delinsCAGG
ENST00000549606.5:c.-157-1057_-157-1054delinsCAGG	ENSP00000447005.1:n.-157-1057_-157-1054delinsCAGG
ENST00000550419.5:c.525_528delinsCAGG	ENSP00000448098.1:p.Thr175=
ENST00000551888.5:n.458+95_458+98delinsCAGG
ENST00000553237.5:c.*271+95_*271+98delinsCAGG	ENSP00000448885.1:n.*271+95_*271+98delinsCAGG
NM_000075.3:c.632+95_632+98delinsCAGG	NP_000066.1:n.632+95_632+98delinsCAGG
NM_000075.4:c.632+95_632+98delinsCAGG MANE Select	NP_000066.1:n.632+95_632+98delinsCAGG