Canonical Allele Identifier: CA10186464
Community Standard Title: NM_001303256.3(MORC2):c.3031-4C>G
Gene: MORC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30926875G>C , CM000684.2:g.30926875G>C GRCh38
NC_000022.10:g.31322862G>C , CM000684.1:g.31322862G>C GRCh37
NC_000022.9:g.29652862G>C NCBI36
NG_046752.1:g.46623C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001303256.3:c.3031-4C>G MANE Select NP_001290185.1:n.3031-4C>G
ENST00000397641.8:c.3031-4C>G MANE Select ENSP00000380763.2:n.3031-4C>G
NM_001303256.1:c.3031-4C>G NP_001290185.1:n.3031-4C>G
NM_001303256.2:c.3031-4C>G NP_001290185.1:n.3031-4C>G
NM_001303257.1:c.3022-4C>G NP_001290186.1:n.3022-4C>G
NM_001303257.2:c.3022-4C>G NP_001290186.1:n.3022-4C>G
NM_014941.2:c.2845-4C>G NP_055756.1:n.2845-4C>G
NM_014941.3:c.2845-4C>G NP_055756.1:n.2845-4C>G
ENST00000215862.8:c.2845-4C>G ENSP00000215862.4:n.2845-4C>G
ENST00000397641.7:c.3031-4C>G ENSP00000380763.2:n.3031-4C>G
ENST00000429468.5:c.202-4C>G ENSP00000412685.1:n.202-4C>G
ENST00000445980.5:c.506-4C>G
ENST00000674576.1:n.4477-4C>G
ENST00000674585.1:n.707-4C>G
ENST00000675027.1:n.1564C>G
ENST00000675317.1:n.1443-4C>G
ENST00000675402.1:n.663-4C>G
ENST00000675570.1:c.878-4C>G
ENST00000675601.1:n.2873-4C>G
ENST00000675779.1:c.653-4C>G ENSP00000502216.1:n.653-4C>G
ENST00000675798.1:n.783-4C>G
ENST00000676215.1:n.3874-4C>G
ENST00000676263.1:n.1276-4C>G
XM_011530003.1:c.3055-4C>G XP_011528305.1:n.3055-4C>G
XM_011530004.1:c.3046-4C>G XP_011528306.1:n.3046-4C>G
XM_011530004.2:c.3046-4C>G XP_011528306.1:n.3046-4C>G
XM_011530005.1:c.3046-4C>G XP_011528307.1:n.3046-4C>G
XM_011530006.1:c.2896-4C>G XP_011528308.1:n.2896-4C>G
XM_017028667.2:c.3037-4C>G XP_016884156.1:n.3037-4C>G