Canonical Allele Identifier: CA411238937

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30937914T>C , CM000684.2:g.30937914T>C	GRCh38
NC_000022.10:g.31333901T>C , CM000684.1:g.31333901T>C	GRCh37
NC_000022.9:g.29663901T>C	NCBI36
NG_046752.1:g.35584A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.1270A>G MANE Select	NP_001290185.1:p.Thr424Ala
ENST00000397641.8:c.1270A>G MANE Select	ENSP00000380763.2:p.Thr424Ala
NM_001303256.1:c.1270A>G	NP_001290185.1:p.Thr424Ala
NM_001303256.2:c.1270A>G	NP_001290185.1:p.Thr424Ala
NM_001303257.1:c.1270A>G	NP_001290186.1:p.Thr424Ala
NM_001303257.2:c.1270A>G	NP_001290186.1:p.Thr424Ala
NM_014941.2:c.1084A>G	NP_055756.1:p.Thr362Ala
NM_014941.3:c.1084A>G	NP_055756.1:p.Thr362Ala
ENST00000215862.8:c.1084A>G	ENSP00000215862.4:p.Thr362Ala
ENST00000397641.7:c.1270A>G	ENSP00000380763.2:p.Thr424Ala
ENST00000469915.1:n.459-912A>G
ENST00000674576.1:n.2716A>G
ENST00000675601.1:n.1112A>G
ENST00000676215.1:n.2113A>G
XM_011530003.1:c.1294A>G	XP_011528305.1:p.Thr432Ala
XM_011530004.1:c.1285A>G	XP_011528306.1:p.Thr429Ala
XM_011530004.2:c.1285A>G	XP_011528306.1:p.Thr429Ala
XM_011530005.1:c.1294A>G	XP_011528307.1:p.Thr432Ala
XM_011530006.1:c.1135A>G	XP_011528308.1:p.Thr379Ala
XM_017028667.2:c.1285A>G	XP_016884156.1:p.Thr429Ala