Canonical Allele Identifier: CA408196857
Gene: MCM8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5967473G>A , CM000682.2:g.5967473G>A GRCh38
NC_000020.10:g.5948119G>A , CM000682.1:g.5948119G>A GRCh37
NC_000020.9:g.5896119G>A NCBI36
NG_042869.1:g.21822G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652720.1:c.913G>A ENSP00000498784.1:p.Gly305Ser
ENST00000265187.4:c.913G>A ENSP00000265187.4:p.Gly305Ser
ENST00000378883.5:c.913G>A ENSP00000368161.1:p.Gly305Ser
ENST00000378886.6:c.913G>A ENSP00000368164.2:p.Gly305Ser
ENST00000378896.7:c.913G>A ENSP00000368174.3:p.Gly305Ser
ENST00000610722.4:c.913G>A MANE Select ENSP00000478141.1:p.Gly305Ser
NM_001281520.1:c.913G>A NP_001268449.1:p.Gly305Ser
NM_001281521.1:c.913G>A NP_001268450.1:p.Gly305Ser
NM_001281522.1:c.913G>A NP_001268451.1:p.Gly305Ser
NM_032485.5:c.913G>A NP_115874.3:p.Gly305Ser
NM_182802.2:c.913G>A NP_877954.1:p.Gly305Ser
XM_011529387.1:c.913G>A XP_011527689.1:p.Gly305Ser
XR_937169.1:n.1253G>A
XM_011529387.2:c.913G>A XP_011527689.1:p.Gly305Ser
XM_017028105.1:c.913G>A XP_016883594.1:p.Gly305Ser
XM_017028106.1:c.721G>A XP_016883595.1:p.Gly241Ser
XM_017028107.1:c.64G>A XP_016883596.1:p.Gly22Ser
XR_001754422.1:n.1253G>A
XR_001754423.1:n.1253G>A
NM_032485.6:c.913G>A MANE Select NP_115874.3:p.Gly305Ser
NM_182802.3:c.913G>A NP_877954.1:p.Gly305Ser
NM_001281520.2:c.913G>A NP_001268449.1:p.Gly305Ser
NM_001281521.2:c.913G>A NP_001268450.1:p.Gly305Ser
NM_001281522.2:c.913G>A NP_001268451.1:p.Gly305Ser