Canonical Allele Identifier: CA2619494792

Gene: CDK4

Linked Data

• dbSNP Id: rs763476153
• gnomAD v4: 12-57750795-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750795C>A , CM000674.2:g.57750795C>A	GRCh38
NC_000012.11:g.58144578C>A , CM000674.1:g.58144578C>A	GRCh37
NC_000012.10:g.56430845C>A	NCBI36
NG_007484.2:g.6587G>T , LRG_490:g.6587G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.523-30G>T MANE Select	ENSP00000257904.5:n.523-30G>T
ENST00000257904.10:c.523-30G>T	ENSP00000257904.5:n.523-30G>T
ENST00000312990.10:c.265-124G>T	ENSP00000316889.6:n.265-124G>T
ENST00000546489.5:c.301-30G>T	ENSP00000447779.1:n.301-30G>T
ENST00000547281.5:c.301-30G>T	ENSP00000447274.1:n.301-30G>T
ENST00000549606.5:c.-157-1291G>T	ENSP00000447005.1:n.-157-1291G>T
ENST00000550419.5:c.522+128G>T	ENSP00000448098.1:n.522+128G>T
ENST00000551800.5:c.301-30G>T	ENSP00000449391.1:n.301-30G>T
ENST00000551888.5:n.443-124G>T
ENST00000552254.5:c.523-30G>T	ENSP00000449179.1:n.523-30G>T
ENST00000553237.5:c.*162-30G>T	ENSP00000448885.1:n.*162-30G>T
NM_000075.3:c.523-30G>T	NP_000066.1:n.523-30G>T
NM_000075.4:c.523-30G>T MANE Select	NP_000066.1:n.523-30G>T