Canonical Allele Identifier: CA408197447

Gene: MCM8

Linked Data

• gnomAD v4: 20-5967560-A-T
• MyVariant Identifiers: chr20:g.5948206A>T (hg19) ; chr20:g.5967560A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.5967560A>T , CM000682.2:g.5967560A>T	GRCh38
NC_000020.10:g.5948206A>T , CM000682.1:g.5948206A>T	GRCh37
NC_000020.9:g.5896206A>T	NCBI36
NG_042869.1:g.21909A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652720.1:c.1000A>T	ENSP00000498784.1:p.Ile334Phe
ENST00000265187.4:c.1000A>T	ENSP00000265187.4:p.Ile334Phe
ENST00000378883.5:c.1000A>T	ENSP00000368161.1:p.Ile334Phe
ENST00000378886.6:c.1000A>T	ENSP00000368164.2:p.Ile334Phe
ENST00000378896.7:c.1000A>T	ENSP00000368174.3:p.Ile334Phe
ENST00000610722.4:c.1000A>T MANE Select	ENSP00000478141.1:p.Ile334Phe
NM_001281520.1:c.1000A>T	NP_001268449.1:p.Ile334Phe
NM_001281521.1:c.1000A>T	NP_001268450.1:p.Ile334Phe
NM_001281522.1:c.1000A>T	NP_001268451.1:p.Ile334Phe
NM_032485.5:c.1000A>T	NP_115874.3:p.Ile334Phe
NM_182802.2:c.1000A>T	NP_877954.1:p.Ile334Phe
XM_011529387.1:c.1000A>T	XP_011527689.1:p.Ile334Phe
XR_937169.1:n.1340A>T
XM_011529387.2:c.1000A>T	XP_011527689.1:p.Ile334Phe
XM_017028105.1:c.1000A>T	XP_016883594.1:p.Ile334Phe
XM_017028106.1:c.808A>T	XP_016883595.1:p.Ile270Phe
XM_017028107.1:c.151A>T	XP_016883596.1:p.Ile51Phe
XR_001754422.1:n.1340A>T
XR_001754423.1:n.1340A>T
NM_032485.6:c.1000A>T MANE Select	NP_115874.3:p.Ile334Phe
NM_182802.3:c.1000A>T	NP_877954.1:p.Ile334Phe
NM_001281520.2:c.1000A>T	NP_001268449.1:p.Ile334Phe
NM_001281521.2:c.1000A>T	NP_001268450.1:p.Ile334Phe
NM_001281522.2:c.1000A>T	NP_001268451.1:p.Ile334Phe