Canonical Allele Identifier: CA10186994

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30937810A>T , CM000684.2:g.30937810A>T	GRCh38
NC_000022.10:g.31333797A>T , CM000684.1:g.31333797A>T	GRCh37
NC_000022.9:g.29663797A>T	NCBI36
NG_046752.1:g.35688T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.1369+5T>A MANE Select	NP_001290185.1:n.1369+5T>A
ENST00000397641.8:c.1369+5T>A MANE Select	ENSP00000380763.2:n.1369+5T>A
NM_001303256.1:c.1369+5T>A	NP_001290185.1:n.1369+5T>A
NM_001303256.2:c.1369+5T>A	NP_001290185.1:n.1369+5T>A
NM_001303257.1:c.1369+5T>A	NP_001290186.1:n.1369+5T>A
NM_001303257.2:c.1369+5T>A	NP_001290186.1:n.1369+5T>A
NM_014941.2:c.1183+5T>A	NP_055756.1:n.1183+5T>A
NM_014941.3:c.1183+5T>A	NP_055756.1:n.1183+5T>A
ENST00000215862.8:c.1183+5T>A	ENSP00000215862.4:n.1183+5T>A
ENST00000397641.7:c.1369+5T>A	ENSP00000380763.2:n.1369+5T>A
ENST00000469915.1:n.459-808T>A
ENST00000674576.1:n.2815+5T>A
ENST00000675601.1:n.1211+5T>A
ENST00000676215.1:n.2212+5T>A
XM_011530003.1:c.1393+5T>A	XP_011528305.1:n.1393+5T>A
XM_011530004.1:c.1384+5T>A	XP_011528306.1:n.1384+5T>A
XM_011530004.2:c.1384+5T>A	XP_011528306.1:n.1384+5T>A
XM_011530005.1:c.1393+5T>A	XP_011528307.1:n.1393+5T>A
XM_011530006.1:c.1234+5T>A	XP_011528308.1:n.1234+5T>A
XM_017028667.2:c.1384+5T>A	XP_016884156.1:n.1384+5T>A