Canonical Allele Identifier: CA208421194

Gene: CDK1

Linked Data

• dbSNP Id: rs538733917
• gnomAD v3: 10-60788548-C-T
• gnomAD v4: 10-60788548-C-T
• MyVariant Identifiers: chr10:g.62548306C>T (hg19) ; chr10:g.60788548C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60788548C>T , CM000672.2:g.60788548C>T	GRCh38
NC_000010.10:g.62548306C>T , CM000672.1:g.62548306C>T	GRCh37
NC_000010.9:g.62218312C>T	NCBI36
NG_029877.1:g.15218C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395284.8:c.489+318C>T MANE Select	ENSP00000378699.3:n.489+318C>T
ENST00000316629.8:c.318+2761C>T	ENSP00000325970.4:n.318+2761C>T
ENST00000373809.2:c.318+2761C>T	ENSP00000362915.2:n.318+2761C>T
ENST00000395284.7:c.489+318C>T	ENSP00000378699.3:n.489+318C>T
ENST00000448257.6:c.493+314C>T	ENSP00000397973.2:n.493+314C>T
ENST00000487784.1:n.564+314C>T
ENST00000519078.6:c.489+318C>T	ENSP00000430665.2:n.489+318C>T
ENST00000614696.4:c.489+318C>T	ENSP00000482996.1:n.489+318C>T
NM_001786.4:c.489+318C>T	NP_001777.1:n.489+318C>T
NM_033379.4:c.318+2761C>T	NP_203698.1:n.318+2761C>T
XM_005270303.2:c.489+318C>T	XP_005270360.1:n.489+318C>T
XM_006718082.1:c.489+318C>T	XP_006718145.1:n.489+318C>T
NM_001320918.1:c.489+318C>T	NP_001307847.1:n.489+318C>T
XM_005270303.3:c.489+318C>T	XP_005270360.1:n.489+318C>T
NM_001786.5:c.489+318C>T MANE Select	NP_001777.1:n.489+318C>T
NM_033379.5:c.318+2761C>T	NP_203698.1:n.318+2761C>T