Canonical Allele Identifier: CA480404349

Gene: CDK4

Linked Data

• dbSNP Id: rs2140386280
• MyVariant Identifiers: chr12:g.58144706C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750923C>A , CM000674.2:g.57750923C>A	GRCh38
NC_000012.11:g.58144706C>A , CM000674.1:g.58144706C>A	GRCh37
NC_000012.10:g.56430973C>A	NCBI36
NG_007484.2:g.6459G>T , LRG_490:g.6459G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.522G>T MANE Select	ENSP00000257904.5:p.Val174=
ENST00000257904.10:c.522G>T	ENSP00000257904.5:p.Val174=
ENST00000312990.10:c.265-252G>T	ENSP00000316889.6:n.265-252G>T
ENST00000546489.5:c.300G>T	ENSP00000447779.1:p.Val100=
ENST00000547281.5:c.300G>T	ENSP00000447274.1:p.Val100=
ENST00000549606.5:c.-158+1252G>T	ENSP00000447005.1:n.-158+1252G>T
ENST00000550419.5:c.522G>T	ENSP00000448098.1:p.Val174=
ENST00000551706.1:n.888G>T
ENST00000551800.5:c.300G>T	ENSP00000449391.1:p.Val100=
ENST00000551888.5:n.443-252G>T
ENST00000552254.5:c.522G>T	ENSP00000449179.1:p.Val174=
ENST00000553237.5:c.*161G>T	ENSP00000448885.1:n.*161G>T
NM_000075.3:c.522G>T	NP_000066.1:p.Val174=
NM_000075.4:c.522G>T MANE Select	NP_000066.1:p.Val174=