Canonical Allele Identifier: CA10187136

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30940768T>C , CM000684.2:g.30940768T>C	GRCh38
NC_000022.10:g.31336755T>C , CM000684.1:g.31336755T>C	GRCh37
NC_000022.9:g.29666755T>C	NCBI36
NG_046752.1:g.32730A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.894A>G MANE Select	NP_001290185.1:p.Val298=
ENST00000397641.8:c.894A>G MANE Select	ENSP00000380763.2:p.Val298=
NM_001303256.1:c.894A>G	NP_001290185.1:p.Val298=
NM_001303256.2:c.894A>G	NP_001290185.1:p.Val298=
NM_001303257.1:c.894A>G	NP_001290186.1:p.Val298=
NM_001303257.2:c.894A>G	NP_001290186.1:p.Val298=
NM_014941.2:c.708A>G	NP_055756.1:p.Val236=
NM_014941.3:c.708A>G	NP_055756.1:p.Val236=
ENST00000215862.8:c.708A>G	ENSP00000215862.4:p.Val236=
ENST00000397641.7:c.894A>G	ENSP00000380763.2:p.Val298=
ENST00000469915.1:n.448A>G
ENST00000675601.1:n.736A>G
ENST00000676215.1:n.70A>G
XM_011530003.1:c.918A>G	XP_011528305.1:p.Val306=
XM_011530004.1:c.909A>G	XP_011528306.1:p.Val303=
XM_011530004.2:c.909A>G	XP_011528306.1:p.Val303=
XM_011530005.1:c.918A>G	XP_011528307.1:p.Val306=
XM_011530006.1:c.759A>G	XP_011528308.1:p.Val253=
XM_017028667.2:c.909A>G	XP_016884156.1:p.Val303=