Canonical Allele Identifier: CA411246232

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30950416T>C , CM000684.2:g.30950416T>C	GRCh38
NC_000022.10:g.31346402T>C , CM000684.1:g.31346402T>C	GRCh37
NC_000022.9:g.29676402T>C	NCBI36
NG_046752.1:g.23082A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.187A>G MANE Select	NP_001290185.1:p.Met63Val
ENST00000397641.8:c.187A>G MANE Select	ENSP00000380763.2:p.Met63Val
NM_001303256.1:c.187A>G	NP_001290185.1:p.Met63Val
NM_001303256.2:c.187A>G	NP_001290185.1:p.Met63Val
NM_001303257.1:c.187A>G	NP_001290186.1:p.Met63Val
NM_001303257.2:c.187A>G	NP_001290186.1:p.Met63Val
NM_014941.2:c.1A>G	NP_055756.1:p.Met1Val
NM_014941.3:c.1A>G	NP_055756.1:p.Met1Val
ENST00000215862.8:c.1A>G	ENSP00000215862.4:p.Met1Val
ENST00000397641.7:c.187A>G	ENSP00000380763.2:p.Met63Val
ENST00000476152.2:n.309A>G
XM_011530003.1:c.211A>G	XP_011528305.1:p.Met71Val
XM_011530004.1:c.202A>G	XP_011528306.1:p.Met68Val
XM_011530004.2:c.202A>G	XP_011528306.1:p.Met68Val
XM_011530005.1:c.211A>G	XP_011528307.1:p.Met71Val
XM_011530006.1:c.52A>G	XP_011528308.1:p.Met18Val
XM_017028667.2:c.202A>G	XP_016884156.1:p.Met68Val