Canonical Allele Identifier: CA237844839

Gene: CDK4

Linked Data

• dbSNP Id: rs891748121
• gnomAD v3: 12-57752198-G-T
• gnomAD v4: 12-57752198-G-T
• MyVariant Identifiers: chr12:g.58145981G>T (hg19) ; chr12:g.57752198G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57752198G>T , CM000674.2:g.57752198G>T	GRCh38
NC_000012.11:g.58145981G>T , CM000674.1:g.58145981G>T	GRCh37
NC_000012.10:g.56432248G>T	NCBI36
NG_007484.2:g.5184C>A , LRG_490:g.5184C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.-43C>A MANE Select	ENSP00000257904.5:n.-43C>A
ENST00000257904.10:c.-43C>A	ENSP00000257904.5:n.-43C>A
ENST00000312990.10:c.-43C>A	ENSP00000316889.6:n.-43C>A
ENST00000546489.5:c.-28C>A	ENSP00000447779.1:n.-28C>A
ENST00000547281.5:c.-188C>A	ENSP00000447274.1:n.-188C>A
ENST00000549606.5:c.-181C>A	ENSP00000447005.1:n.-181C>A
ENST00000550419.5:c.-43C>A	ENSP00000448098.1:n.-43C>A
ENST00000551706.1:n.167C>A
ENST00000551800.5:c.-225C>A	ENSP00000449391.1:n.-225C>A
ENST00000551888.5:n.136C>A
ENST00000552388.1:c.-59C>A	ENSP00000448963.1:n.-59C>A
ENST00000552862.1:c.-19-462C>A	ENSP00000446763.1:n.-19-462C>A
ENST00000553237.5:c.-43C>A	ENSP00000448885.1:n.-43C>A
NM_000075.3:c.-43C>A	NP_000066.1:n.-43C>A
NM_000075.4:c.-43C>A MANE Select	NP_000066.1:n.-43C>A