Canonical Allele Identifier: CA15634430
Gene: CDK1 HGNC NCBI

Linked Data

dbSNP Id: rs3213056
gnomAD v2: 10-62548390-G-A
gnomAD v3: 10-60788632-G-A
gnomAD v4: 10-60788632-G-A
MyVariant Identifiers: chr10:g.62548390G>A (hg19) chr10:g.60788632G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60788632G>A , CM000672.2:g.60788632G>A GRCh38
NC_000010.10:g.62548390G>A , CM000672.1:g.62548390G>A GRCh37
NC_000010.9:g.62218396G>A NCBI36
NG_029877.1:g.15302G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395284.8:c.489+402G>A MANE Select ENSP00000378699.3:n.489+402G>A
ENST00000316629.8:c.318+2845G>A ENSP00000325970.4:n.318+2845G>A
ENST00000373809.2:c.318+2845G>A ENSP00000362915.2:n.318+2845G>A
ENST00000395284.7:c.489+402G>A ENSP00000378699.3:n.489+402G>A
ENST00000448257.6:c.493+398G>A ENSP00000397973.2:n.493+398G>A
ENST00000487784.1:n.564+398G>A
ENST00000519078.6:c.489+402G>A ENSP00000430665.2:n.489+402G>A
ENST00000614696.4:c.489+402G>A ENSP00000482996.1:n.489+402G>A
NM_001786.4:c.489+402G>A NP_001777.1:n.489+402G>A
NM_033379.4:c.318+2845G>A NP_203698.1:n.318+2845G>A
XM_005270303.2:c.489+402G>A XP_005270360.1:n.489+402G>A
XM_006718082.1:c.489+402G>A XP_006718145.1:n.489+402G>A
NM_001320918.1:c.489+402G>A NP_001307847.1:n.489+402G>A
XM_005270303.3:c.489+402G>A XP_005270360.1:n.489+402G>A
NM_001786.5:c.489+402G>A MANE Select NP_001777.1:n.489+402G>A
NM_033379.5:c.318+2845G>A NP_203698.1:n.318+2845G>A
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