Canonical Allele Identifier: CA2651839750
Gene: MCM8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5967524_5967525insAAAAT , CM000682.2:g.5967524_5967525insAAAAT GRCh38
NC_000020.10:g.5948170_5948171insAAAAT , CM000682.1:g.5948170_5948171insAAAAT GRCh37
NC_000020.9:g.5896170_5896171insAAAAT NCBI36
NG_042869.1:g.21873_21874insAAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000652720.1:c.964_965insAAAAT ENSP00000498784.1:p.Ser322LysfsTer10
ENST00000265187.4:c.964_965insAAAAT ENSP00000265187.4:p.Ser322LysfsTer10
ENST00000378883.5:c.964_965insAAAAT ENSP00000368161.1:p.Ser322LysfsTer10
ENST00000378886.6:c.964_965insAAAAT ENSP00000368164.2:p.Ser322LysfsTer10
ENST00000378896.7:c.964_965insAAAAT ENSP00000368174.3:p.Ser322LysfsTer10
ENST00000610722.4:c.964_965insAAAAT MANE Select ENSP00000478141.1:p.Ser322LysfsTer10
NM_001281520.1:c.964_965insAAAAT NP_001268449.1:p.Ser322LysfsTer10
NM_001281521.1:c.964_965insAAAAT NP_001268450.1:p.Ser322LysfsTer10
NM_001281522.1:c.964_965insAAAAT NP_001268451.1:p.Ser322LysfsTer10
NM_032485.5:c.964_965insAAAAT NP_115874.3:p.Ser322LysfsTer10
NM_182802.2:c.964_965insAAAAT NP_877954.1:p.Ser322LysfsTer10
XM_011529387.1:c.964_965insAAAAT XP_011527689.1:p.Ser322LysfsTer10
XR_937169.1:n.1304_1305insAAAAT
XM_011529387.2:c.964_965insAAAAT XP_011527689.1:p.Ser322LysfsTer10
XM_017028105.1:c.964_965insAAAAT XP_016883594.1:p.Ser322LysfsTer10
XM_017028106.1:c.772_773insAAAAT XP_016883595.1:p.Ser258LysfsTer10
XM_017028107.1:c.115_116insAAAAT XP_016883596.1:p.Ser39LysfsTer10
XR_001754422.1:n.1304_1305insAAAAT
XR_001754423.1:n.1304_1305insAAAAT
NM_032485.6:c.964_965insAAAAT MANE Select NP_115874.3:p.Ser322LysfsTer10
NM_182802.3:c.964_965insAAAAT NP_877954.1:p.Ser322LysfsTer10
NM_001281520.2:c.964_965insAAAAT NP_001268449.1:p.Ser322LysfsTer10
NM_001281521.2:c.964_965insAAAAT NP_001268450.1:p.Ser322LysfsTer10
NM_001281522.2:c.964_965insAAAAT NP_001268451.1:p.Ser322LysfsTer10