Canonical Allele Identifier: CA2347744833
Gene: MCM8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5967581G= , CM000682.2:g.5967581G= GRCh38
NC_000020.10:g.5948227G= , CM000682.1:g.5948227G= GRCh37
NC_000020.9:g.5896227G= NCBI36
NG_042869.1:g.21930G=

Transcript Alleles

HGVS Amino-acid change
ENST00000652720.1:c.1021G= ENSP00000498784.1:p.Glu341=
ENST00000265187.4:c.1021G= ENSP00000265187.4:p.Glu341=
ENST00000378883.5:c.1021G= ENSP00000368161.1:p.Glu341=
ENST00000378886.6:c.1021G= ENSP00000368164.2:p.Glu341=
ENST00000378896.7:c.1021G= ENSP00000368174.3:p.Glu341=
ENST00000610722.4:c.1021G= MANE Select ENSP00000478141.1:p.Glu341=
NM_001281520.1:c.1021G= NP_001268449.1:p.Glu341=
NM_001281521.1:c.1021G= NP_001268450.1:p.Glu341=
NM_001281522.1:c.1021G= NP_001268451.1:p.Glu341=
NM_032485.5:c.1021G= NP_115874.3:p.Glu341=
NM_182802.2:c.1021G= NP_877954.1:p.Glu341=
XM_011529387.1:c.1021G= XP_011527689.1:p.Glu341=
XR_937169.1:n.1361G=
XM_011529387.2:c.1021G= XP_011527689.1:p.Glu341=
XM_017028105.1:c.1021G= XP_016883594.1:p.Glu341=
XM_017028106.1:c.829G= XP_016883595.1:p.Glu277=
XM_017028107.1:c.172G= XP_016883596.1:p.Glu58=
XR_001754422.1:n.1361G=
XR_001754423.1:n.1361G=
NM_032485.6:c.1021G= MANE Select NP_115874.3:p.Glu341=
NM_182802.3:c.1021G= NP_877954.1:p.Glu341=
NM_001281520.2:c.1021G= NP_001268449.1:p.Glu341=
NM_001281521.2:c.1021G= NP_001268450.1:p.Glu341=
NM_001281522.2:c.1021G= NP_001268451.1:p.Glu341=