Canonical Allele Identifier: CA10187355

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30950427C>T , CM000684.2:g.30950427C>T	GRCh38
NC_000022.10:g.31346413C>T , CM000684.1:g.31346413C>T	GRCh37
NC_000022.9:g.29676413C>T	NCBI36
NG_046752.1:g.23071G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.176G>A MANE Select	NP_001290185.1:p.Arg59Gln
ENST00000397641.8:c.176G>A MANE Select	ENSP00000380763.2:p.Arg59Gln
NM_001303256.1:c.176G>A	NP_001290185.1:p.Arg59Gln
NM_001303256.2:c.176G>A	NP_001290185.1:p.Arg59Gln
NM_001303257.1:c.176G>A	NP_001290186.1:p.Arg59Gln
NM_001303257.2:c.176G>A	NP_001290186.1:p.Arg59Gln
NM_014941.2:c.-11G>A	NP_055756.1:n.-11G>A
NM_014941.3:c.-11G>A	NP_055756.1:n.-11G>A
ENST00000215862.8:c.-11G>A	ENSP00000215862.4:n.-11G>A
ENST00000397641.7:c.176G>A	ENSP00000380763.2:p.Arg59Gln
ENST00000476152.2:n.298G>A
XM_011530003.1:c.200G>A	XP_011528305.1:p.Arg67Gln
XM_011530004.1:c.191G>A	XP_011528306.1:p.Arg64Gln
XM_011530004.2:c.191G>A	XP_011528306.1:p.Arg64Gln
XM_011530005.1:c.200G>A	XP_011528307.1:p.Arg67Gln
XM_011530006.1:c.41G>A	XP_011528308.1:p.Arg14Gln
XM_017028667.2:c.191G>A	XP_016884156.1:p.Arg64Gln