Canonical Allele Identifier: CA10843855

Gene: CDC7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91500888A>G , CM000663.2:g.91500888A>G	GRCh38
NC_000001.10:g.91966445A>G , CM000663.1:g.91966445A>G	GRCh37
NC_000001.9:g.91739033A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234626.11:c.-124A>G MANE Select	ENSP00000234626.6:n.-124A>G
NM_001134419.1:c.-90A>G	NP_001127891.1:n.-90A>G
NM_003503.3:c.-124A>G	NP_003494.1:n.-124A>G
XM_005271241.2:c.-64+11A>G	XP_005271298.1:n.-64+11A>G
XM_005271244.2:c.-124A>G	XP_005271301.1:n.-124A>G
XM_005271245.3:c.-124A>G	XP_005271302.1:n.-124A>G
XM_005271244.3:c.-124A>G	XP_005271301.1:n.-124A>G
XM_017002425.2:c.-64+11A>G	XP_016857914.1:n.-64+11A>G
XM_017002426.1:c.-90A>G	XP_016857915.1:n.-90A>G
XM_017002427.2:c.-297A>G	XP_016857916.1:n.-297A>G
XM_024450089.1:c.-63-766A>G	XP_024305857.1:n.-63-766A>G
XR_001737461.1:n.42A>G
XR_001737462.1:n.64+11A>G
NM_003503.4:c.-124A>G MANE Select	NP_003494.1:n.-124A>G
NM_001134419.2:c.-90A>G	NP_001127891.1:n.-90A>G