Canonical Allele Identifier: CA514238850

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30932341A>T , CM000684.2:g.30932341A>T	GRCh38
NC_000022.10:g.31328328A>T , CM000684.1:g.31328328A>T	GRCh37
NC_000022.9:g.29658328A>T	NCBI36
NG_046752.1:g.41157T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397641.8:c.2841+18T>A MANE Select	ENSP00000380763.2:n.2841+18T>A
ENST00000674576.1:n.4287+18T>A
ENST00000674585.1:n.526+18T>A
ENST00000675027.1:n.231+18T>A
ENST00000675317.1:n.1262+18T>A
ENST00000675402.1:n.473+18T>A
ENST00000675570.1:c.697+18T>A
ENST00000675601.1:n.2683+18T>A
ENST00000675779.1:c.189+18T>A	ENSP00000502216.1:n.189+18T>A
ENST00000675798.1:n.593+18T>A
ENST00000676215.1:n.3684+18T>A
ENST00000676263.1:n.1086+18T>A
ENST00000215862.8:c.2655+18T>A	ENSP00000215862.4:n.2655+18T>A
ENST00000397641.7:c.2841+18T>A	ENSP00000380763.2:n.2841+18T>A
ENST00000445980.5:c.325+18T>A
NM_001303256.1:c.2841+18T>A	NP_001290185.1:n.2841+18T>A
NM_001303257.1:c.2841+18T>A	NP_001290186.1:n.2841+18T>A
NM_014941.2:c.2655+18T>A	NP_055756.1:n.2655+18T>A
XM_011530003.1:c.2865+18T>A	XP_011528305.1:n.2865+18T>A
XM_011530004.1:c.2856+18T>A	XP_011528306.1:n.2856+18T>A
XM_011530005.1:c.2865+18T>A	XP_011528307.1:n.2865+18T>A
XM_011530006.1:c.2706+18T>A	XP_011528308.1:n.2706+18T>A
NM_001303256.2:c.2841+18T>A	NP_001290185.1:n.2841+18T>A
NM_001303257.2:c.2841+18T>A	NP_001290186.1:n.2841+18T>A
NM_014941.3:c.2655+18T>A	NP_055756.1:n.2655+18T>A
XM_011530004.2:c.2856+18T>A	XP_011528306.1:n.2856+18T>A
XM_017028667.2:c.2856+18T>A	XP_016884156.1:n.2856+18T>A
NM_001303256.3:c.2841+18T>A MANE Select	NP_001290185.1:n.2841+18T>A