Canonical Allele Identifier: CA2726350958

Gene: CDK4

Linked Data

• dbSNP Id: rs2140386894

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751121G>A , CM000674.2:g.57751121G>A	GRCh38
NC_000012.11:g.58144904G>A , CM000674.1:g.58144904G>A	GRCh37
NC_000012.10:g.56431171G>A	NCBI36
NG_007484.2:g.6261C>T , LRG_490:g.6261C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.355-31C>T MANE Select	ENSP00000257904.5:n.355-31C>T
ENST00000257904.10:c.355-31C>T	ENSP00000257904.5:n.355-31C>T
ENST00000312990.10:c.264+176C>T	ENSP00000316889.6:n.264+176C>T
ENST00000546489.5:c.133-31C>T	ENSP00000447779.1:n.133-31C>T
ENST00000547281.5:c.133-31C>T	ENSP00000447274.1:n.133-31C>T
ENST00000549606.5:c.-158+1054C>T	ENSP00000447005.1:n.-158+1054C>T
ENST00000550419.5:c.355-31C>T	ENSP00000448098.1:n.355-31C>T
ENST00000551706.1:n.721-31C>T
ENST00000551800.5:c.133-31C>T	ENSP00000449391.1:n.133-31C>T
ENST00000551888.5:n.442+176C>T
ENST00000552254.5:c.355-31C>T	ENSP00000449179.1:n.355-31C>T
ENST00000552388.1:c.355-31C>T	ENSP00000448963.1:n.355-31C>T
ENST00000553237.5:c.219-31C>T	ENSP00000448885.1:n.219-31C>T
NM_000075.3:c.355-31C>T	NP_000066.1:n.355-31C>T
NM_000075.4:c.355-31C>T MANE Select	NP_000066.1:n.355-31C>T