Canonical Allele Identifier: CA411245055

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30949777C>T , CM000684.2:g.30949777C>T	GRCh38
NC_000022.10:g.31345763C>T , CM000684.1:g.31345763C>T	GRCh37
NC_000022.9:g.29675763C>T	NCBI36
NG_046752.1:g.23721G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.292G>A MANE Select	NP_001290185.1:p.Gly98Arg
ENST00000397641.8:c.292G>A MANE Select	ENSP00000380763.2:p.Gly98Arg
NM_001303256.1:c.292G>A	NP_001290185.1:p.Gly98Arg
NM_001303256.2:c.292G>A	NP_001290185.1:p.Gly98Arg
NM_001303257.1:c.292G>A	NP_001290186.1:p.Gly98Arg
NM_001303257.2:c.292G>A	NP_001290186.1:p.Gly98Arg
NM_014941.2:c.106G>A	NP_055756.1:p.Gly36Arg
NM_014941.3:c.106G>A	NP_055756.1:p.Gly36Arg
ENST00000215862.8:c.106G>A	ENSP00000215862.4:p.Gly36Arg
ENST00000397641.7:c.292G>A	ENSP00000380763.2:p.Gly98Arg
ENST00000476152.2:n.414G>A
XM_011530003.1:c.316G>A	XP_011528305.1:p.Gly106Arg
XM_011530004.1:c.307G>A	XP_011528306.1:p.Gly103Arg
XM_011530004.2:c.307G>A	XP_011528306.1:p.Gly103Arg
XM_011530005.1:c.316G>A	XP_011528307.1:p.Gly106Arg
XM_011530006.1:c.157G>A	XP_011528308.1:p.Gly53Arg
XM_017028667.2:c.307G>A	XP_016884156.1:p.Gly103Arg