Canonical Allele Identifier: CA2038994379
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs375726467

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750279C>A , CM000674.2:g.57750279C>A GRCh38
NC_000012.11:g.58144062C>A , CM000674.1:g.58144062C>A GRCh37
NC_000012.10:g.56430329C>A NCBI36
NG_007484.2:g.7103G>T , LRG_490:g.7103G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+377G>T MANE Select ENSP00000257904.5:n.632+377G>T
ENST00000257904.10:c.632+377G>T ENSP00000257904.5:n.632+377G>T
ENST00000312990.10:c.280+377G>T ENSP00000316889.6:n.280+377G>T
ENST00000546489.5:c.410+377G>T ENSP00000447779.1:n.410+377G>T
ENST00000547281.5:c.410+377G>T ENSP00000447274.1:n.410+377G>T
ENST00000549606.5:c.-157-775G>T ENSP00000447005.1:n.-157-775G>T
ENST00000550419.5:c.*38+163G>T ENSP00000448098.1:n.*38+163G>T
ENST00000551888.5:n.458+377G>T
ENST00000553237.5:c.*271+377G>T ENSP00000448885.1:n.*271+377G>T
NM_000075.3:c.632+377G>T NP_000066.1:n.632+377G>T
NM_000075.4:c.632+377G>T MANE Select NP_000066.1:n.632+377G>T