Canonical Allele Identifier: CA2038994869
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750607C= , CM000674.2:g.57750607C= GRCh38
NC_000012.11:g.58144390C= , CM000674.1:g.58144390C= GRCh37
NC_000012.10:g.56430657C= NCBI36
NG_007484.2:g.6775G= , LRG_490:g.6775G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+49G= MANE Select ENSP00000257904.5:n.632+49G=
ENST00000257904.10:c.632+49G= ENSP00000257904.5:n.632+49G=
ENST00000312990.10:c.280+49G= ENSP00000316889.6:n.280+49G=
ENST00000546489.5:c.410+49G= ENSP00000447779.1:n.410+49G=
ENST00000547281.5:c.410+49G= ENSP00000447274.1:n.410+49G=
ENST00000549606.5:c.-157-1103G= ENSP00000447005.1:n.-157-1103G=
ENST00000550419.5:c.523-44G= ENSP00000448098.1:n.523-44G=
ENST00000551888.5:n.458+49G=
ENST00000553237.5:c.*271+49G= ENSP00000448885.1:n.*271+49G=
NM_000075.3:c.632+49G= NP_000066.1:n.632+49G=
NM_000075.4:c.632+49G= MANE Select NP_000066.1:n.632+49G=