Canonical Allele Identifier: CA946818

Gene: CDC7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91513109A>G , CM000663.2:g.91513109A>G	GRCh38
NC_000001.10:g.91978666A>G , CM000663.1:g.91978666A>G	GRCh37
NC_000001.9:g.91751254A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234626.11:c.624A>G MANE Select	ENSP00000234626.6:p.Ile208Met
ENST00000234626.10:c.624A>G	ENSP00000234626.6:p.Ile208Met
ENST00000428239.5:c.624A>G	ENSP00000393139.1:p.Ile208Met
NM_001134419.1:c.624A>G	NP_001127891.1:p.Ile208Met
NM_001134420.1:c.624A>G	NP_001127892.1:p.Ile208Met
NM_003503.3:c.624A>G	NP_003494.1:p.Ile208Met
XM_005271241.2:c.624A>G	XP_005271298.1:p.Ile208Met
XM_005271244.2:c.624A>G	XP_005271301.1:p.Ile208Met
XM_005271245.3:c.624A>G	XP_005271302.1:p.Ile208Met
XM_011542226.1:c.624A>G	XP_011540528.1:p.Ile208Met
XM_011542227.1:c.273A>G	XP_011540529.1:p.Ile91Met
XM_005271244.3:c.624A>G	XP_005271301.1:p.Ile208Met
XM_017002425.2:c.624A>G	XP_016857914.1:p.Ile208Met
XM_017002426.1:c.624A>G	XP_016857915.1:p.Ile208Met
XM_017002427.2:c.273A>G	XP_016857916.1:p.Ile91Met
XM_024450089.1:c.624A>G	XP_024305857.1:p.Ile208Met
XM_024450090.1:c.624A>G	XP_024305858.1:p.Ile208Met
XR_001737461.1:n.789A>G
XR_001737462.1:n.751A>G
NM_003503.4:c.624A>G MANE Select	NP_003494.1:p.Ile208Met
NM_001134419.2:c.624A>G	NP_001127891.1:p.Ile208Met
NM_001134420.2:c.624A>G	NP_001127892.1:p.Ile208Met