Canonical Allele Identifier: CA411228892
Community Standard Title: NM_001303256.3(MORC2):c.3031G>A (p.Asp1011Asn)
Gene: MORC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30926871C>T , CM000684.2:g.30926871C>T GRCh38
NC_000022.10:g.31322858C>T , CM000684.1:g.31322858C>T GRCh37
NC_000022.9:g.29652858C>T NCBI36
NG_046752.1:g.46627G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001303256.3:c.3031G>A MANE Select NP_001290185.1:p.Asp1011Asn
ENST00000397641.8:c.3031G>A MANE Select ENSP00000380763.2:p.Asp1011Asn
NM_001303256.1:c.3031G>A NP_001290185.1:p.Asp1011Asn
NM_001303256.2:c.3031G>A NP_001290185.1:p.Asp1011Asn
NM_001303257.1:c.3022G>A NP_001290186.1:p.Asp1008Asn
NM_001303257.2:c.3022G>A NP_001290186.1:p.Asp1008Asn
NM_014941.2:c.2845G>A NP_055756.1:p.Asp949Asn
NM_014941.3:c.2845G>A NP_055756.1:p.Asp949Asn
ENST00000215862.8:c.2845G>A ENSP00000215862.4:p.Asp949Asn
ENST00000397641.7:c.3031G>A ENSP00000380763.2:p.Asp1011Asn
ENST00000429468.5:c.202G>A ENSP00000412685.1:p.Asp68Asn
ENST00000445980.5:c.506G>A
ENST00000674576.1:n.4477G>A
ENST00000674585.1:n.707G>A
ENST00000675027.1:n.1568G>A
ENST00000675317.1:n.1443G>A
ENST00000675402.1:n.663G>A
ENST00000675570.1:c.878G>A
ENST00000675601.1:n.2873G>A
ENST00000675779.1:c.653G>A ENSP00000502216.1:n.653G>A
ENST00000675798.1:n.783G>A
ENST00000676215.1:n.3874G>A
ENST00000676263.1:n.1276G>A
XM_011530003.1:c.3055G>A XP_011528305.1:p.Asp1019Asn
XM_011530004.1:c.3046G>A XP_011528306.1:p.Asp1016Asn
XM_011530004.2:c.3046G>A XP_011528306.1:p.Asp1016Asn
XM_011530005.1:c.3046G>A XP_011528307.1:p.Asp1016Asn
XM_011530006.1:c.2896G>A XP_011528308.1:p.Asp966Asn
XM_017028667.2:c.3037G>A XP_016884156.1:p.Asp1013Asn