Canonical Allele Identifier: CA208421203

Gene: CDK1

Linked Data

• dbSNP Id: rs1005659552
• MyVariant Identifiers: chr10:g.62548385T>C (hg19) ; chr10:g.60788627T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60788627T>C , CM000672.2:g.60788627T>C	GRCh38
NC_000010.10:g.62548385T>C , CM000672.1:g.62548385T>C	GRCh37
NC_000010.9:g.62218391T>C	NCBI36
NG_029877.1:g.15297T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395284.8:c.489+397T>C MANE Select	ENSP00000378699.3:n.489+397T>C
ENST00000316629.8:c.318+2840T>C	ENSP00000325970.4:n.318+2840T>C
ENST00000373809.2:c.318+2840T>C	ENSP00000362915.2:n.318+2840T>C
ENST00000395284.7:c.489+397T>C	ENSP00000378699.3:n.489+397T>C
ENST00000448257.6:c.493+393T>C	ENSP00000397973.2:n.493+393T>C
ENST00000487784.1:n.564+393T>C
ENST00000519078.6:c.489+397T>C	ENSP00000430665.2:n.489+397T>C
ENST00000614696.4:c.489+397T>C	ENSP00000482996.1:n.489+397T>C
NM_001786.4:c.489+397T>C	NP_001777.1:n.489+397T>C
NM_033379.4:c.318+2840T>C	NP_203698.1:n.318+2840T>C
XM_005270303.2:c.489+397T>C	XP_005270360.1:n.489+397T>C
XM_006718082.1:c.489+397T>C	XP_006718145.1:n.489+397T>C
NM_001320918.1:c.489+397T>C	NP_001307847.1:n.489+397T>C
XM_005270303.3:c.489+397T>C	XP_005270360.1:n.489+397T>C
NM_001786.5:c.489+397T>C MANE Select	NP_001777.1:n.489+397T>C
NM_033379.5:c.318+2840T>C	NP_203698.1:n.318+2840T>C