Canonical Allele Identifier: CA2347744786
Gene: MCM8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5967485C= , CM000682.2:g.5967485C= GRCh38
NC_000020.10:g.5948131C= , CM000682.1:g.5948131C= GRCh37
NC_000020.9:g.5896131C= NCBI36
NG_042869.1:g.21834C=

Transcript Alleles

HGVS Amino-acid change
ENST00000652720.1:c.925C= ENSP00000498784.1:p.Arg309=
ENST00000265187.4:c.925C= ENSP00000265187.4:p.Arg309=
ENST00000378883.5:c.925C= ENSP00000368161.1:p.Arg309=
ENST00000378886.6:c.925C= ENSP00000368164.2:p.Arg309=
ENST00000378896.7:c.925C= ENSP00000368174.3:p.Arg309=
ENST00000610722.4:c.925C= MANE Select ENSP00000478141.1:p.Arg309=
NM_001281520.1:c.925C= NP_001268449.1:p.Arg309=
NM_001281521.1:c.925C= NP_001268450.1:p.Arg309=
NM_001281522.1:c.925C= NP_001268451.1:p.Arg309=
NM_032485.5:c.925C= NP_115874.3:p.Arg309=
NM_182802.2:c.925C= NP_877954.1:p.Arg309=
XM_011529387.1:c.925C= XP_011527689.1:p.Arg309=
XR_937169.1:n.1265C=
XM_011529387.2:c.925C= XP_011527689.1:p.Arg309=
XM_017028105.1:c.925C= XP_016883594.1:p.Arg309=
XM_017028106.1:c.733C= XP_016883595.1:p.Arg245=
XM_017028107.1:c.76C= XP_016883596.1:p.Arg26=
XR_001754422.1:n.1265C=
XR_001754423.1:n.1265C=
NM_032485.6:c.925C= MANE Select NP_115874.3:p.Arg309=
NM_182802.3:c.925C= NP_877954.1:p.Arg309=
NM_001281520.2:c.925C= NP_001268449.1:p.Arg309=
NM_001281521.2:c.925C= NP_001268450.1:p.Arg309=
NM_001281522.2:c.925C= NP_001268451.1:p.Arg309=