Canonical Allele Identifier: CA2038994548
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750397C= , CM000674.2:g.57750397C= GRCh38
NC_000012.11:g.58144180C= , CM000674.1:g.58144180C= GRCh37
NC_000012.10:g.56430447C= NCBI36
NG_007484.2:g.6985G= , LRG_490:g.6985G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+259G= MANE Select ENSP00000257904.5:n.632+259G=
ENST00000257904.10:c.632+259G= ENSP00000257904.5:n.632+259G=
ENST00000312990.10:c.280+259G= ENSP00000316889.6:n.280+259G=
ENST00000546489.5:c.410+259G= ENSP00000447779.1:n.410+259G=
ENST00000547281.5:c.410+259G= ENSP00000447274.1:n.410+259G=
ENST00000549606.5:c.-157-893G= ENSP00000447005.1:n.-157-893G=
ENST00000550419.5:c.*38+45G= ENSP00000448098.1:n.*38+45G=
ENST00000551888.5:n.458+259G=
ENST00000553237.5:c.*271+259G= ENSP00000448885.1:n.*271+259G=
NM_000075.3:c.632+259G= NP_000066.1:n.632+259G=
NM_000075.4:c.632+259G= MANE Select NP_000066.1:n.632+259G=