Canonical Allele Identifier: CA746116716
Gene: MCM8 HGNC NCBI

Linked Data

dbSNP Id: rs1299109993

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5968796_5968799del , CM000682.2:g.5968796_5968799del GRCh38
NC_000020.10:g.5949442_5949445del , CM000682.1:g.5949442_5949445del GRCh37
NC_000020.9:g.5897442_5897445del NCBI36
NG_042869.1:g.23145_23148del

Transcript Alleles

HGVS Amino-acid Change
ENST00000652720.1:c.1223+771_1223+774del ENSP00000498784.1:n.1223+771_1223+774del
ENST00000265187.4:c.1175+771_1175+774del ENSP00000265187.4:n.1175+771_1175+774del
ENST00000378883.5:c.1223+771_1223+774del ENSP00000368161.1:n.1223+771_1223+774del
ENST00000378886.6:c.1223+771_1223+774del ENSP00000368164.2:n.1223+771_1223+774del
ENST00000378896.7:c.1223+771_1223+774del ENSP00000368174.3:n.1223+771_1223+774del
ENST00000610722.4:c.1223+771_1223+774del MANE Select ENSP00000478141.1:n.1223+771_1223+774del
NM_001281520.1:c.1223+771_1223+774del NP_001268449.1:n.1223+771_1223+774del
NM_001281521.1:c.1223+771_1223+774del NP_001268450.1:n.1223+771_1223+774del
NM_001281522.1:c.1223+771_1223+774del NP_001268451.1:n.1223+771_1223+774del
NM_032485.5:c.1223+771_1223+774del NP_115874.3:n.1223+771_1223+774del
NM_182802.2:c.1175+771_1175+774del NP_877954.1:n.1175+771_1175+774del
XM_011529387.1:c.1223+771_1223+774del XP_011527689.1:n.1223+771_1223+774del
XR_937169.1:n.1563+771_1563+774del
XM_011529387.2:c.1223+771_1223+774del XP_011527689.1:n.1223+771_1223+774del
XM_017028105.1:c.1223+771_1223+774del XP_016883594.1:n.1223+771_1223+774del
XM_017028106.1:c.1031+771_1031+774del XP_016883595.1:n.1031+771_1031+774del
XM_017028107.1:c.374+771_374+774del XP_016883596.1:n.374+771_374+774del
XR_001754422.1:n.1563+771_1563+774del
XR_001754423.1:n.1563+771_1563+774del
NM_032485.6:c.1223+771_1223+774del MANE Select NP_115874.3:n.1223+771_1223+774del
NM_182802.3:c.1175+771_1175+774del NP_877954.1:n.1175+771_1175+774del
NM_001281520.2:c.1223+771_1223+774del NP_001268449.1:n.1223+771_1223+774del
NM_001281521.2:c.1223+771_1223+774del NP_001268450.1:n.1223+771_1223+774del
NM_001281522.2:c.1223+771_1223+774del NP_001268451.1:n.1223+771_1223+774del