Canonical Allele Identifier: CA2575206295

Gene: CDK4

Linked Data

• gnomAD v4: 12-57751438-CCCCACCTATAGGCTGTCTTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751442_57751462del , CM000674.2:g.57751442_57751462del	GRCh38
NC_000012.11:g.58145225_58145245del , CM000674.1:g.58145225_58145245del	GRCh37
NC_000012.10:g.56431492_56431512del	NCBI36
NG_007484.2:g.5923_5943del , LRG_490:g.5923_5943del

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.218+41_218+61del MANE Select	ENSP00000257904.5:n.218+41_218+61del
ENST00000257904.10:c.218+41_218+61del	ENSP00000257904.5:n.218+41_218+61del
ENST00000312990.10:c.218+41_218+61del	ENSP00000316889.6:n.218+41_218+61del
ENST00000546489.5:c.-4-117_-4-97del	ENSP00000447779.1:n.-4-117_-4-97del
ENST00000547281.5:c.-5+41_-5+61del	ENSP00000447274.1:n.-5+41_-5+61del
ENST00000549606.5:c.-158+716_-158+736del	ENSP00000447005.1:n.-158+716_-158+736del
ENST00000550419.5:c.218+41_218+61del	ENSP00000448098.1:n.218+41_218+61del
ENST00000551706.1:n.468_488del
ENST00000551800.5:c.-5+41_-5+61del	ENSP00000449391.1:n.-5+41_-5+61del
ENST00000551888.5:n.396+41_396+61del
ENST00000552254.5:c.218+41_218+61del	ENSP00000449179.1:n.218+41_218+61del
ENST00000552388.1:c.218+41_218+61del	ENSP00000448963.1:n.218+41_218+61del
ENST00000552862.1:c.218+41_218+61del	ENSP00000446763.1:n.218+41_218+61del
ENST00000553237.5:c.218+41_218+61del	ENSP00000448885.1:n.218+41_218+61del
NM_000075.3:c.218+41_218+61del	NP_000066.1:n.218+41_218+61del
NM_000075.4:c.218+41_218+61del MANE Select	NP_000066.1:n.218+41_218+61del