Canonical Allele Identifier: CA408197115
Gene: MCM8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.5967519T>C , CM000682.2:g.5967519T>C GRCh38
NC_000020.10:g.5948165T>C , CM000682.1:g.5948165T>C GRCh37
NC_000020.9:g.5896165T>C NCBI36
NG_042869.1:g.21868T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000652720.1:c.959T>C ENSP00000498784.1:p.Val320Ala
ENST00000265187.4:c.959T>C ENSP00000265187.4:p.Val320Ala
ENST00000378883.5:c.959T>C ENSP00000368161.1:p.Val320Ala
ENST00000378886.6:c.959T>C ENSP00000368164.2:p.Val320Ala
ENST00000378896.7:c.959T>C ENSP00000368174.3:p.Val320Ala
ENST00000610722.4:c.959T>C MANE Select ENSP00000478141.1:p.Val320Ala
NM_001281520.1:c.959T>C NP_001268449.1:p.Val320Ala
NM_001281521.1:c.959T>C NP_001268450.1:p.Val320Ala
NM_001281522.1:c.959T>C NP_001268451.1:p.Val320Ala
NM_032485.5:c.959T>C NP_115874.3:p.Val320Ala
NM_182802.2:c.959T>C NP_877954.1:p.Val320Ala
XM_011529387.1:c.959T>C XP_011527689.1:p.Val320Ala
XR_937169.1:n.1299T>C
XM_011529387.2:c.959T>C XP_011527689.1:p.Val320Ala
XM_017028105.1:c.959T>C XP_016883594.1:p.Val320Ala
XM_017028106.1:c.767T>C XP_016883595.1:p.Val256Ala
XM_017028107.1:c.110T>C XP_016883596.1:p.Val37Ala
XR_001754422.1:n.1299T>C
XR_001754423.1:n.1299T>C
NM_032485.6:c.959T>C MANE Select NP_115874.3:p.Val320Ala
NM_182802.3:c.959T>C NP_877954.1:p.Val320Ala
NM_001281520.2:c.959T>C NP_001268449.1:p.Val320Ala
NM_001281521.2:c.959T>C NP_001268450.1:p.Val320Ala
NM_001281522.2:c.959T>C NP_001268451.1:p.Val320Ala