Canonical Allele Identifier: CA10186604

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30932648C>T , CM000684.2:g.30932648C>T	GRCh38
NC_000022.10:g.31328635C>T , CM000684.1:g.31328635C>T	GRCh37
NC_000022.9:g.29658635C>T	NCBI36
NG_046752.1:g.40850G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.2644G>A MANE Select	NP_001290185.1:p.Ala882Thr
ENST00000397641.8:c.2644G>A MANE Select	ENSP00000380763.2:p.Ala882Thr
NM_001303256.1:c.2644G>A	NP_001290185.1:p.Ala882Thr
NM_001303256.2:c.2644G>A	NP_001290185.1:p.Ala882Thr
NM_001303257.1:c.2644G>A	NP_001290186.1:p.Ala882Thr
NM_001303257.2:c.2644G>A	NP_001290186.1:p.Ala882Thr
NM_014941.2:c.2458G>A	NP_055756.1:p.Ala820Thr
NM_014941.3:c.2458G>A	NP_055756.1:p.Ala820Thr
ENST00000215862.8:c.2458G>A	ENSP00000215862.4:p.Ala820Thr
ENST00000397641.7:c.2644G>A	ENSP00000380763.2:p.Ala882Thr
ENST00000445980.5:c.128G>A
ENST00000674576.1:n.4090G>A
ENST00000674585.1:n.329G>A
ENST00000675027.1:n.34G>A
ENST00000675317.1:n.1065G>A
ENST00000675402.1:n.276G>A
ENST00000675570.1:c.500G>A
ENST00000675601.1:n.2486G>A
ENST00000675798.1:n.396G>A
ENST00000676215.1:n.3487G>A
ENST00000676263.1:n.889G>A
XM_011530003.1:c.2668G>A	XP_011528305.1:p.Ala890Thr
XM_011530004.1:c.2659G>A	XP_011528306.1:p.Ala887Thr
XM_011530004.2:c.2659G>A	XP_011528306.1:p.Ala887Thr
XM_011530005.1:c.2668G>A	XP_011528307.1:p.Ala890Thr
XM_011530006.1:c.2509G>A	XP_011528308.1:p.Ala837Thr
XM_017028667.2:c.2659G>A	XP_016884156.1:p.Ala887Thr