Canonical Allele Identifier: CA2347744826

Gene: MCM8

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.5967554A= , CM000682.2:g.5967554A=	GRCh38
NC_000020.10:g.5948200A= , CM000682.1:g.5948200A=	GRCh37
NC_000020.9:g.5896200A=	NCBI36
NG_042869.1:g.21903A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652720.1:c.994A=	ENSP00000498784.1:p.Thr332=
ENST00000265187.4:c.994A=	ENSP00000265187.4:p.Thr332=
ENST00000378883.5:c.994A=	ENSP00000368161.1:p.Thr332=
ENST00000378886.6:c.994A=	ENSP00000368164.2:p.Thr332=
ENST00000378896.7:c.994A=	ENSP00000368174.3:p.Thr332=
ENST00000610722.4:c.994A= MANE Select	ENSP00000478141.1:p.Thr332=
NM_001281520.1:c.994A=	NP_001268449.1:p.Thr332=
NM_001281521.1:c.994A=	NP_001268450.1:p.Thr332=
NM_001281522.1:c.994A=	NP_001268451.1:p.Thr332=
NM_032485.5:c.994A=	NP_115874.3:p.Thr332=
NM_182802.2:c.994A=	NP_877954.1:p.Thr332=
XM_011529387.1:c.994A=	XP_011527689.1:p.Thr332=
XR_937169.1:n.1334A=
XM_011529387.2:c.994A=	XP_011527689.1:p.Thr332=
XM_017028105.1:c.994A=	XP_016883594.1:p.Thr332=
XM_017028106.1:c.802A=	XP_016883595.1:p.Thr268=
XM_017028107.1:c.145A=	XP_016883596.1:p.Thr49=
XR_001754422.1:n.1334A=
XR_001754423.1:n.1334A=
NM_032485.6:c.994A= MANE Select	NP_115874.3:p.Thr332=
NM_182802.3:c.994A=	NP_877954.1:p.Thr332=
NM_001281520.2:c.994A=	NP_001268449.1:p.Thr332=
NM_001281521.2:c.994A=	NP_001268450.1:p.Thr332=
NM_001281522.2:c.994A=	NP_001268451.1:p.Thr332=