Canonical Allele Identifier: CA385547876

Gene: CDK4

Linked Data

• dbSNP Id: rs1955234097
• MyVariant Identifiers: chr12:g.58145050C>G (hg19) ; chr12:g.57751267C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751267C>G , CM000674.2:g.57751267C>G	GRCh38
NC_000012.11:g.58145050C>G , CM000674.1:g.58145050C>G	GRCh37
NC_000012.10:g.56431317C>G	NCBI36
NG_007484.2:g.6115G>C , LRG_490:g.6115G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.294G>C MANE Select	ENSP00000257904.5:p.Gln98His
ENST00000257904.10:c.294G>C	ENSP00000257904.5:p.Gln98His
ENST00000312990.10:c.264+30G>C	ENSP00000316889.6:n.264+30G>C
ENST00000546489.5:c.72G>C	ENSP00000447779.1:p.Gln24His
ENST00000547281.5:c.72G>C	ENSP00000447274.1:p.Gln24His
ENST00000549606.5:c.-158+908G>C	ENSP00000447005.1:n.-158+908G>C
ENST00000550419.5:c.294G>C	ENSP00000448098.1:p.Gln98His
ENST00000551706.1:n.660G>C
ENST00000551800.5:c.72G>C	ENSP00000449391.1:p.Gln24His
ENST00000551888.5:n.442+30G>C
ENST00000552254.5:c.294G>C	ENSP00000449179.1:p.Gln98His
ENST00000552388.1:c.294G>C	ENSP00000448963.1:p.Gln98His
ENST00000552862.1:c.294G>C	ENSP00000446763.1:p.Gln98His
ENST00000553237.5:c.219-177G>C	ENSP00000448885.1:n.219-177G>C
NM_000075.3:c.294G>C	NP_000066.1:p.Gln98His
NM_000075.4:c.294G>C MANE Select	NP_000066.1:p.Gln98His