Canonical Allele Identifier: CA6657787

Gene: CDK4

Linked Data

• dbSNP Id: rs371812067
• ExAC: 12:58144575 G / T
• gnomAD v2: 12-58144575-G-T
• gnomAD v4: 12-57750792-G-T
• MyVariant Identifiers: chr12:g.58144575G>T (hg19) ; chr12:g.57750792G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750792G>T , CM000674.2:g.57750792G>T	GRCh38
NC_000012.11:g.58144575G>T , CM000674.1:g.58144575G>T	GRCh37
NC_000012.10:g.56430842G>T	NCBI36
NG_007484.2:g.6590C>A , LRG_490:g.6590C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.523-27C>A MANE Select	ENSP00000257904.5:n.523-27C>A
ENST00000257904.10:c.523-27C>A	ENSP00000257904.5:n.523-27C>A
ENST00000312990.10:c.265-121C>A	ENSP00000316889.6:n.265-121C>A
ENST00000546489.5:c.301-27C>A	ENSP00000447779.1:n.301-27C>A
ENST00000547281.5:c.301-27C>A	ENSP00000447274.1:n.301-27C>A
ENST00000549606.5:c.-157-1288C>A	ENSP00000447005.1:n.-157-1288C>A
ENST00000550419.5:c.522+131C>A	ENSP00000448098.1:n.522+131C>A
ENST00000551800.5:c.301-27C>A	ENSP00000449391.1:n.301-27C>A
ENST00000551888.5:n.443-121C>A
ENST00000552254.5:c.523-27C>A	ENSP00000449179.1:n.523-27C>A
ENST00000553237.5:c.*162-27C>A	ENSP00000448885.1:n.*162-27C>A
NM_000075.3:c.523-27C>A	NP_000066.1:n.523-27C>A
NM_000075.4:c.523-27C>A MANE Select	NP_000066.1:n.523-27C>A