Canonical Allele Identifier: CA10187142
Gene: MORC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 542290
dbSNP Id: rs764379949

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30940823G>A , CM000684.2:g.30940823G>A GRCh38
NC_000022.10:g.31336810G>A , CM000684.1:g.31336810G>A GRCh37
NC_000022.9:g.29666810G>A NCBI36
NG_046752.1:g.32675C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000397641.8:c.839C>T MANE Select ENSP00000380763.2:p.Thr280Met
ENST00000675601.1:n.681C>T
ENST00000676215.1:n.15C>T
ENST00000215862.8:c.653C>T ENSP00000215862.4:p.Thr218Met
ENST00000397641.7:c.839C>T ENSP00000380763.2:p.Thr280Met
ENST00000469915.1:n.393C>T
NM_001303256.1:c.839C>T NP_001290185.1:p.Thr280Met
NM_001303257.1:c.839C>T NP_001290186.1:p.Thr280Met
NM_014941.2:c.653C>T NP_055756.1:p.Thr218Met
XM_011530003.1:c.863C>T XP_011528305.1:p.Thr288Met
XM_011530004.1:c.854C>T XP_011528306.1:p.Thr285Met
XM_011530005.1:c.863C>T XP_011528307.1:p.Thr288Met
XM_011530006.1:c.704C>T XP_011528308.1:p.Thr235Met
NM_001303256.2:c.839C>T NP_001290185.1:p.Thr280Met
NM_001303257.2:c.839C>T NP_001290186.1:p.Thr280Met
NM_014941.3:c.653C>T NP_055756.1:p.Thr218Met
XM_011530004.2:c.854C>T XP_011528306.1:p.Thr285Met
XM_017028667.2:c.854C>T XP_016884156.1:p.Thr285Met
NM_001303256.3:c.839C>T MANE Select NP_001290185.1:p.Thr280Met