Canonical Allele Identifier: CA10186593

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30932615G>A , CM000684.2:g.30932615G>A	GRCh38
NC_000022.10:g.31328602G>A , CM000684.1:g.31328602G>A	GRCh37
NC_000022.9:g.29658602G>A	NCBI36
NG_046752.1:g.40883C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.2677C>T MANE Select	NP_001290185.1:p.Arg893Cys
ENST00000397641.8:c.2677C>T MANE Select	ENSP00000380763.2:p.Arg893Cys
NM_001303256.1:c.2677C>T	NP_001290185.1:p.Arg893Cys
NM_001303256.2:c.2677C>T	NP_001290185.1:p.Arg893Cys
NM_001303257.1:c.2677C>T	NP_001290186.1:p.Arg893Cys
NM_001303257.2:c.2677C>T	NP_001290186.1:p.Arg893Cys
NM_014941.2:c.2491C>T	NP_055756.1:p.Arg831Cys
NM_014941.3:c.2491C>T	NP_055756.1:p.Arg831Cys
ENST00000215862.8:c.2491C>T	ENSP00000215862.4:p.Arg831Cys
ENST00000397641.7:c.2677C>T	ENSP00000380763.2:p.Arg893Cys
ENST00000445980.5:c.161C>T
ENST00000674576.1:n.4123C>T
ENST00000674585.1:n.362C>T
ENST00000675027.1:n.67C>T
ENST00000675317.1:n.1098C>T
ENST00000675402.1:n.309C>T
ENST00000675570.1:c.533C>T
ENST00000675601.1:n.2519C>T
ENST00000675779.1:c.25C>T	ENSP00000502216.1:p.Arg9Cys
ENST00000675798.1:n.429C>T
ENST00000676215.1:n.3520C>T
ENST00000676263.1:n.922C>T
XM_011530003.1:c.2701C>T	XP_011528305.1:p.Arg901Cys
XM_011530004.1:c.2692C>T	XP_011528306.1:p.Arg898Cys
XM_011530004.2:c.2692C>T	XP_011528306.1:p.Arg898Cys
XM_011530005.1:c.2701C>T	XP_011528307.1:p.Arg901Cys
XM_011530006.1:c.2542C>T	XP_011528308.1:p.Arg848Cys
XM_017028667.2:c.2692C>T	XP_016884156.1:p.Arg898Cys