Canonical Allele Identifier: CA385545591

Gene: CDK4

Linked Data

• ClinVar Variation Id: 1751922
• ClinVar RCV Id: RCV002353629
• MyVariant Identifiers: chr12:g.58144456T>C (hg19) ; chr12:g.57750673T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750673T>C , CM000674.2:g.57750673T>C	GRCh38
NC_000012.11:g.58144456T>C , CM000674.1:g.58144456T>C	GRCh37
NC_000012.10:g.56430723T>C	NCBI36
NG_007484.2:g.6709A>G , LRG_490:g.6709A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.615A>G MANE Select	ENSP00000257904.5:p.Ala205=
ENST00000257904.10:c.615A>G	ENSP00000257904.5:p.Ala205=
ENST00000312990.10:c.265-2A>G	ENSP00000316889.6:n.265-2A>G
ENST00000546489.5:c.393A>G	ENSP00000447779.1:p.Ala131=
ENST00000547281.5:c.393A>G	ENSP00000447274.1:p.Ala131=
ENST00000549606.5:c.-157-1169A>G	ENSP00000447005.1:n.-157-1169A>G
ENST00000550419.5:c.523-110A>G	ENSP00000448098.1:n.523-110A>G
ENST00000551800.5:c.393A>G	ENSP00000449391.1:p.Ala131=
ENST00000551888.5:n.443-2A>G
ENST00000553237.5:c.*254A>G	ENSP00000448885.1:n.*254A>G
NM_000075.3:c.615A>G	NP_000066.1:p.Ala205=
NM_000075.4:c.615A>G MANE Select	NP_000066.1:p.Ala205=