Canonical Allele Identifier: CA10186519

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30928161T>C , CM000684.2:g.30928161T>C	GRCh38
NC_000022.10:g.31324148T>C , CM000684.1:g.31324148T>C	GRCh37
NC_000022.9:g.29654148T>C	NCBI36
NG_046752.1:g.45337A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.2888A>G MANE Select	NP_001290185.1:p.Asn963Ser
ENST00000397641.8:c.2888A>G MANE Select	ENSP00000380763.2:p.Asn963Ser
NM_001303256.1:c.2888A>G	NP_001290185.1:p.Asn963Ser
NM_001303256.2:c.2888A>G	NP_001290185.1:p.Asn963Ser
NM_001303257.1:c.2888A>G	NP_001290186.1:p.Asn963Ser
NM_001303257.2:c.2888A>G	NP_001290186.1:p.Asn963Ser
NM_014941.2:c.2702A>G	NP_055756.1:p.Asn901Ser
NM_014941.3:c.2702A>G	NP_055756.1:p.Asn901Ser
ENST00000215862.8:c.2702A>G	ENSP00000215862.4:p.Asn901Ser
ENST00000397641.7:c.2888A>G	ENSP00000380763.2:p.Asn963Ser
ENST00000429468.5:c.68A>G	ENSP00000412685.1:p.Asn23Ser
ENST00000445980.5:c.372A>G
ENST00000674576.1:n.4334A>G
ENST00000674585.1:n.573A>G
ENST00000675027.1:n.278A>G
ENST00000675317.1:n.1309A>G
ENST00000675402.1:n.520A>G
ENST00000675570.1:c.744A>G
ENST00000675601.1:n.2730A>G
ENST00000675779.1:c.236A>G	ENSP00000502216.1:p.Asn79Ser
ENST00000675798.1:n.640A>G
ENST00000676215.1:n.3731A>G
ENST00000676263.1:n.1133A>G
XM_011530003.1:c.2912A>G	XP_011528305.1:p.Asn971Ser
XM_011530004.1:c.2903A>G	XP_011528306.1:p.Asn968Ser
XM_011530004.2:c.2903A>G	XP_011528306.1:p.Asn968Ser
XM_011530005.1:c.2912A>G	XP_011528307.1:p.Asn971Ser
XM_011530006.1:c.2753A>G	XP_011528308.1:p.Asn918Ser
XM_017028667.2:c.2903A>G	XP_016884156.1:p.Asn968Ser