Canonical Allele Identifier: CA385545586

Gene: CDK4

Linked Data

• dbSNP Id: rs2140385630
• MyVariant Identifiers: chr12:g.58144455C>T (hg19) ; chr12:g.57750672C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750672C>T , CM000674.2:g.57750672C>T	GRCh38
NC_000012.11:g.58144455C>T , CM000674.1:g.58144455C>T	GRCh37
NC_000012.10:g.56430722C>T	NCBI36
NG_007484.2:g.6710G>A , LRG_490:g.6710G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.616G>A MANE Select	ENSP00000257904.5:p.Glu206Lys
ENST00000257904.10:c.616G>A	ENSP00000257904.5:p.Glu206Lys
ENST00000312990.10:c.265-1G>A	ENSP00000316889.6:n.265-1G>A
ENST00000546489.5:c.394G>A	ENSP00000447779.1:p.Glu132Lys
ENST00000547281.5:c.394G>A	ENSP00000447274.1:p.Glu132Lys
ENST00000549606.5:c.-157-1168G>A	ENSP00000447005.1:n.-157-1168G>A
ENST00000550419.5:c.523-109G>A	ENSP00000448098.1:n.523-109G>A
ENST00000551800.5:c.394G>A	ENSP00000449391.1:p.Glu132Lys
ENST00000551888.5:n.443-1G>A
ENST00000553237.5:c.*255G>A	ENSP00000448885.1:n.*255G>A
NM_000075.3:c.616G>A	NP_000066.1:p.Glu206Lys
NM_000075.4:c.616G>A MANE Select	NP_000066.1:p.Glu206Lys