Canonical Allele Identifier: CA10187306
Community Standard Title: NM_001303256.3(MORC2):c.227-5T>C
Gene: MORC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30949847A>G , CM000684.2:g.30949847A>G GRCh38
NC_000022.10:g.31345833A>G , CM000684.1:g.31345833A>G GRCh37
NC_000022.9:g.29675833A>G NCBI36
NG_046752.1:g.23651T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001303256.3:c.227-5T>C MANE Select NP_001290185.1:n.227-5T>C
ENST00000397641.8:c.227-5T>C MANE Select ENSP00000380763.2:n.227-5T>C
NM_001303256.1:c.227-5T>C NP_001290185.1:n.227-5T>C
NM_001303256.2:c.227-5T>C NP_001290185.1:n.227-5T>C
NM_001303257.1:c.227-5T>C NP_001290186.1:n.227-5T>C
NM_001303257.2:c.227-5T>C NP_001290186.1:n.227-5T>C
NM_014941.2:c.41-5T>C NP_055756.1:n.41-5T>C
NM_014941.3:c.41-5T>C NP_055756.1:n.41-5T>C
ENST00000215862.8:c.41-5T>C ENSP00000215862.4:n.41-5T>C
ENST00000397641.7:c.227-5T>C ENSP00000380763.2:n.227-5T>C
ENST00000476152.2:n.349-5T>C
XM_011530003.1:c.251-5T>C XP_011528305.1:n.251-5T>C
XM_011530004.1:c.242-5T>C XP_011528306.1:n.242-5T>C
XM_011530004.2:c.242-5T>C XP_011528306.1:n.242-5T>C
XM_011530005.1:c.251-5T>C XP_011528307.1:n.251-5T>C
XM_011530006.1:c.92-5T>C XP_011528308.1:n.92-5T>C
XM_017028667.2:c.242-5T>C XP_016884156.1:n.242-5T>C