Canonical Allele Identifier: CA2651839783

Gene: MCM8

Linked Data

• gnomAD v4: 20-5967645-TTTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.5967647_5967650del , CM000682.2:g.5967647_5967650del	GRCh38
NC_000020.10:g.5948293_5948296del , CM000682.1:g.5948293_5948296del	GRCh37
NC_000020.9:g.5896293_5896296del	NCBI36
NG_042869.1:g.21996_21999del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652720.1:c.1027+60_1027+63del	ENSP00000498784.1:n.1027+60_1027+63del
ENST00000265187.4:c.1027+60_1027+63del	ENSP00000265187.4:n.1027+60_1027+63del
ENST00000378883.5:c.1027+60_1027+63del	ENSP00000368161.1:n.1027+60_1027+63del
ENST00000378886.6:c.1027+60_1027+63del	ENSP00000368164.2:n.1027+60_1027+63del
ENST00000378896.7:c.1027+60_1027+63del	ENSP00000368174.3:n.1027+60_1027+63del
ENST00000610722.4:c.1027+60_1027+63del MANE Select	ENSP00000478141.1:n.1027+60_1027+63del
NM_001281520.1:c.1027+60_1027+63del	NP_001268449.1:n.1027+60_1027+63del
NM_001281521.1:c.1027+60_1027+63del	NP_001268450.1:n.1027+60_1027+63del
NM_001281522.1:c.1027+60_1027+63del	NP_001268451.1:n.1027+60_1027+63del
NM_032485.5:c.1027+60_1027+63del	NP_115874.3:n.1027+60_1027+63del
NM_182802.2:c.1027+60_1027+63del	NP_877954.1:n.1027+60_1027+63del
XM_011529387.1:c.1027+60_1027+63del	XP_011527689.1:n.1027+60_1027+63del
XR_937169.1:n.1367+60_1367+63del
XM_011529387.2:c.1027+60_1027+63del	XP_011527689.1:n.1027+60_1027+63del
XM_017028105.1:c.1027+60_1027+63del	XP_016883594.1:n.1027+60_1027+63del
XM_017028106.1:c.835+60_835+63del	XP_016883595.1:n.835+60_835+63del
XM_017028107.1:c.178+60_178+63del	XP_016883596.1:n.178+60_178+63del
XR_001754422.1:n.1367+60_1367+63del
XR_001754423.1:n.1367+60_1367+63del
NM_032485.6:c.1027+60_1027+63del MANE Select	NP_115874.3:n.1027+60_1027+63del
NM_182802.3:c.1027+60_1027+63del	NP_877954.1:n.1027+60_1027+63del
NM_001281520.2:c.1027+60_1027+63del	NP_001268449.1:n.1027+60_1027+63del
NM_001281521.2:c.1027+60_1027+63del	NP_001268450.1:n.1027+60_1027+63del
NM_001281522.2:c.1027+60_1027+63del	NP_001268451.1:n.1027+60_1027+63del