Canonical Allele Identifier: CA2837143710

Gene: MCM8

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.5968796T>C , CM000682.2:g.5968796T>C	GRCh38
NC_000020.10:g.5949442T>C , CM000682.1:g.5949442T>C	GRCh37
NC_000020.9:g.5897442T>C	NCBI36
NG_042869.1:g.23145T>C

Transcript Alleles

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