Canonical Allele Identifier: CA411238829

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30937892G>A , CM000684.2:g.30937892G>A	GRCh38
NC_000022.10:g.31333879G>A , CM000684.1:g.31333879G>A	GRCh37
NC_000022.9:g.29663879G>A	NCBI36
NG_046752.1:g.35606C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.1292C>T MANE Select	NP_001290185.1:p.Ala431Val
ENST00000397641.8:c.1292C>T MANE Select	ENSP00000380763.2:p.Ala431Val
NM_001303256.1:c.1292C>T	NP_001290185.1:p.Ala431Val
NM_001303256.2:c.1292C>T	NP_001290185.1:p.Ala431Val
NM_001303257.1:c.1292C>T	NP_001290186.1:p.Ala431Val
NM_001303257.2:c.1292C>T	NP_001290186.1:p.Ala431Val
NM_014941.2:c.1106C>T	NP_055756.1:p.Ala369Val
NM_014941.3:c.1106C>T	NP_055756.1:p.Ala369Val
ENST00000215862.8:c.1106C>T	ENSP00000215862.4:p.Ala369Val
ENST00000397641.7:c.1292C>T	ENSP00000380763.2:p.Ala431Val
ENST00000469915.1:n.459-890C>T
ENST00000674576.1:n.2738C>T
ENST00000675601.1:n.1134C>T
ENST00000676215.1:n.2135C>T
XM_011530003.1:c.1316C>T	XP_011528305.1:p.Ala439Val
XM_011530004.1:c.1307C>T	XP_011528306.1:p.Ala436Val
XM_011530004.2:c.1307C>T	XP_011528306.1:p.Ala436Val
XM_011530005.1:c.1316C>T	XP_011528307.1:p.Ala439Val
XM_011530006.1:c.1157C>T	XP_011528308.1:p.Ala386Val
XM_017028667.2:c.1307C>T	XP_016884156.1:p.Ala436Val