Canonical Allele Identifier: CA411245171

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30949806G>A , CM000684.2:g.30949806G>A	GRCh38
NC_000022.10:g.31345792G>A , CM000684.1:g.31345792G>A	GRCh37
NC_000022.9:g.29675792G>A	NCBI36
NG_046752.1:g.23692C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.263C>T MANE Select	NP_001290185.1:p.Ala88Val
ENST00000397641.8:c.263C>T MANE Select	ENSP00000380763.2:p.Ala88Val
NM_001303256.1:c.263C>T	NP_001290185.1:p.Ala88Val
NM_001303256.2:c.263C>T	NP_001290185.1:p.Ala88Val
NM_001303257.1:c.263C>T	NP_001290186.1:p.Ala88Val
NM_001303257.2:c.263C>T	NP_001290186.1:p.Ala88Val
NM_014941.2:c.77C>T	NP_055756.1:p.Ala26Val
NM_014941.3:c.77C>T	NP_055756.1:p.Ala26Val
ENST00000215862.8:c.77C>T	ENSP00000215862.4:p.Ala26Val
ENST00000397641.7:c.263C>T	ENSP00000380763.2:p.Ala88Val
ENST00000476152.2:n.385C>T
XM_011530003.1:c.287C>T	XP_011528305.1:p.Ala96Val
XM_011530004.1:c.278C>T	XP_011528306.1:p.Ala93Val
XM_011530004.2:c.278C>T	XP_011528306.1:p.Ala93Val
XM_011530005.1:c.287C>T	XP_011528307.1:p.Ala96Val
XM_011530006.1:c.128C>T	XP_011528308.1:p.Ala43Val
XM_017028667.2:c.278C>T	XP_016884156.1:p.Ala93Val