Canonical Allele Identifier: CA2619498190

Gene: CDK4

Linked Data

• gnomAD v4: 12-57752196-G-T

Genomic Alleles

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

Transcript Alleles

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