Canonical Allele Identifier: CA10186600

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30932642C>T , CM000684.2:g.30932642C>T	GRCh38
NC_000022.10:g.31328629C>T , CM000684.1:g.31328629C>T	GRCh37
NC_000022.9:g.29658629C>T	NCBI36
NG_046752.1:g.40856G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.2650G>A MANE Select	NP_001290185.1:p.Ala884Thr
ENST00000397641.8:c.2650G>A MANE Select	ENSP00000380763.2:p.Ala884Thr
NM_001303256.1:c.2650G>A	NP_001290185.1:p.Ala884Thr
NM_001303256.2:c.2650G>A	NP_001290185.1:p.Ala884Thr
NM_001303257.1:c.2650G>A	NP_001290186.1:p.Ala884Thr
NM_001303257.2:c.2650G>A	NP_001290186.1:p.Ala884Thr
NM_014941.2:c.2464G>A	NP_055756.1:p.Ala822Thr
NM_014941.3:c.2464G>A	NP_055756.1:p.Ala822Thr
ENST00000215862.8:c.2464G>A	ENSP00000215862.4:p.Ala822Thr
ENST00000397641.7:c.2650G>A	ENSP00000380763.2:p.Ala884Thr
ENST00000445980.5:c.134G>A
ENST00000674576.1:n.4096G>A
ENST00000674585.1:n.335G>A
ENST00000675027.1:n.40G>A
ENST00000675317.1:n.1071G>A
ENST00000675402.1:n.282G>A
ENST00000675570.1:c.506G>A
ENST00000675601.1:n.2492G>A
ENST00000675798.1:n.402G>A
ENST00000676215.1:n.3493G>A
ENST00000676263.1:n.895G>A
XM_011530003.1:c.2674G>A	XP_011528305.1:p.Ala892Thr
XM_011530004.1:c.2665G>A	XP_011528306.1:p.Ala889Thr
XM_011530004.2:c.2665G>A	XP_011528306.1:p.Ala889Thr
XM_011530005.1:c.2674G>A	XP_011528307.1:p.Ala892Thr
XM_011530006.1:c.2515G>A	XP_011528308.1:p.Ala839Thr
XM_017028667.2:c.2665G>A	XP_016884156.1:p.Ala889Thr