Canonical Allele Identifier: CA237844834

Gene: CDK4

Linked Data

• dbSNP Id: rs894064468
• gnomAD v4: 12-57752196-G-A
• MyVariant Identifiers: chr12:g.58145979G>A (hg19) ; chr12:g.57752196G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57752196G>A , CM000674.2:g.57752196G>A	GRCh38
NC_000012.11:g.58145979G>A , CM000674.1:g.58145979G>A	GRCh37
NC_000012.10:g.56432246G>A	NCBI36
NG_007484.2:g.5186C>T , LRG_490:g.5186C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.-41C>T MANE Select	ENSP00000257904.5:n.-41C>T
ENST00000257904.10:c.-41C>T	ENSP00000257904.5:n.-41C>T
ENST00000312990.10:c.-41C>T	ENSP00000316889.6:n.-41C>T
ENST00000546489.5:c.-26C>T	ENSP00000447779.1:n.-26C>T
ENST00000547281.5:c.-186C>T	ENSP00000447274.1:n.-186C>T
ENST00000549606.5:c.-179C>T	ENSP00000447005.1:n.-179C>T
ENST00000550419.5:c.-41C>T	ENSP00000448098.1:n.-41C>T
ENST00000551706.1:n.169C>T
ENST00000551800.5:c.-223C>T	ENSP00000449391.1:n.-223C>T
ENST00000551888.5:n.138C>T
ENST00000552388.1:c.-57C>T	ENSP00000448963.1:n.-57C>T
ENST00000552862.1:c.-19-460C>T	ENSP00000446763.1:n.-19-460C>T
ENST00000553237.5:c.-41C>T	ENSP00000448885.1:n.-41C>T
NM_000075.3:c.-41C>T	NP_000066.1:n.-41C>T
NM_000075.4:c.-41C>T MANE Select	NP_000066.1:n.-41C>T