Canonical Allele Identifier: CA385545558

Gene: CDK4

Linked Data

• ClinVar Variation Id: 845161
• ClinVar RCV Id: RCV001048178
• dbSNP Id: rs1339920302
• gnomAD v2: 12-58144451-A-G
• gnomAD v4: 12-57750668-A-G
• MyVariant Identifiers: chr12:g.58144451A>G (hg19) ; chr12:g.57750668A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750668A>G , CM000674.2:g.57750668A>G	GRCh38
NC_000012.11:g.58144451A>G , CM000674.1:g.58144451A>G	GRCh37
NC_000012.10:g.56430718A>G	NCBI36
NG_007484.2:g.6714T>C , LRG_490:g.6714T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.620T>C MANE Select	ENSP00000257904.5:p.Met207Thr
ENST00000257904.10:c.620T>C	ENSP00000257904.5:p.Met207Thr
ENST00000312990.10:c.268T>C	ENSP00000316889.6:p.Cys90Arg
ENST00000546489.5:c.398T>C	ENSP00000447779.1:p.Met133Thr
ENST00000547281.5:c.398T>C	ENSP00000447274.1:p.Met133Thr
ENST00000549606.5:c.-157-1164T>C	ENSP00000447005.1:n.-157-1164T>C
ENST00000550419.5:c.523-105T>C	ENSP00000448098.1:n.523-105T>C
ENST00000551888.5:n.446T>C
ENST00000553237.5:c.*259T>C	ENSP00000448885.1:n.*259T>C
NM_000075.3:c.620T>C	NP_000066.1:p.Met207Thr
NM_000075.4:c.620T>C MANE Select	NP_000066.1:p.Met207Thr