Canonical Allele Identifier: CA2038997858
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57752191G= , CM000674.2:g.57752191G= GRCh38
NC_000012.11:g.58145974G= , CM000674.1:g.58145974G= GRCh37
NC_000012.10:g.56432241G= NCBI36
NG_007484.2:g.5191C= , LRG_490:g.5191C=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.-36C= MANE Select ENSP00000257904.5:n.-36C=
ENST00000257904.10:c.-36C= ENSP00000257904.5:n.-36C=
ENST00000312990.10:c.-36C= ENSP00000316889.6:n.-36C=
ENST00000546489.5:c.-21C= ENSP00000447779.1:n.-21C=
ENST00000547281.5:c.-181C= ENSP00000447274.1:n.-181C=
ENST00000549606.5:c.-174C= ENSP00000447005.1:n.-174C=
ENST00000550419.5:c.-36C= ENSP00000448098.1:n.-36C=
ENST00000551706.1:n.174C=
ENST00000551800.5:c.-218C= ENSP00000449391.1:n.-218C=
ENST00000551888.5:n.143C=
ENST00000552388.1:c.-52C= ENSP00000448963.1:n.-52C=
ENST00000552862.1:c.-19-455C= ENSP00000446763.1:n.-19-455C=
ENST00000553237.5:c.-36C= ENSP00000448885.1:n.-36C=
NM_000075.3:c.-36C= NP_000066.1:n.-36C=
NM_000075.4:c.-36C= MANE Select NP_000066.1:n.-36C=