Canonical Allele Identifier: CA10186553
Community Standard Title: NM_001303256.3(MORC2):c.2776A>G (p.Ser926Gly)
Gene: MORC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30932424T>C , CM000684.2:g.30932424T>C GRCh38
NC_000022.10:g.31328411T>C , CM000684.1:g.31328411T>C GRCh37
NC_000022.9:g.29658411T>C NCBI36
NG_046752.1:g.41074A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001303256.3:c.2776A>G MANE Select NP_001290185.1:p.Ser926Gly
ENST00000397641.8:c.2776A>G MANE Select ENSP00000380763.2:p.Ser926Gly
NM_001303256.1:c.2776A>G NP_001290185.1:p.Ser926Gly
NM_001303256.2:c.2776A>G NP_001290185.1:p.Ser926Gly
NM_001303257.1:c.2776A>G NP_001290186.1:p.Ser926Gly
NM_001303257.2:c.2776A>G NP_001290186.1:p.Ser926Gly
NM_014941.2:c.2590A>G NP_055756.1:p.Ser864Gly
NM_014941.3:c.2590A>G NP_055756.1:p.Ser864Gly
ENST00000215862.8:c.2590A>G ENSP00000215862.4:p.Ser864Gly
ENST00000397641.7:c.2776A>G ENSP00000380763.2:p.Ser926Gly
ENST00000445980.5:c.260A>G
ENST00000674576.1:n.4222A>G
ENST00000674585.1:n.461A>G
ENST00000675027.1:n.166A>G
ENST00000675317.1:n.1197A>G
ENST00000675402.1:n.408A>G
ENST00000675570.1:c.632A>G
ENST00000675601.1:n.2618A>G
ENST00000675779.1:c.124A>G ENSP00000502216.1:p.Ser42Gly
ENST00000675798.1:n.528A>G
ENST00000676215.1:n.3619A>G
ENST00000676263.1:n.1021A>G
XM_011530003.1:c.2800A>G XP_011528305.1:p.Ser934Gly
XM_011530004.1:c.2791A>G XP_011528306.1:p.Ser931Gly
XM_011530004.2:c.2791A>G XP_011528306.1:p.Ser931Gly
XM_011530005.1:c.2800A>G XP_011528307.1:p.Ser934Gly
XM_011530006.1:c.2641A>G XP_011528308.1:p.Ser881Gly
XM_017028667.2:c.2791A>G XP_016884156.1:p.Ser931Gly