Canonical Allele Identifier: CA514239547

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30941492G>A , CM000684.2:g.30941492G>A	GRCh38
NC_000022.10:g.31337479G>A , CM000684.1:g.31337479G>A	GRCh37
NC_000022.9:g.29667479G>A	NCBI36
NG_046752.1:g.32006C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397641.8:c.765C>T MANE Select	ENSP00000380763.2:p.Ile255=
ENST00000675601.1:n.607C>T
ENST00000215862.8:c.579C>T	ENSP00000215862.4:p.Ile193=
ENST00000397641.7:c.765C>T	ENSP00000380763.2:p.Ile255=
ENST00000469915.1:n.319C>T
NM_001303256.1:c.765C>T	NP_001290185.1:p.Ile255=
NM_001303257.1:c.765C>T	NP_001290186.1:p.Ile255=
NM_014941.2:c.579C>T	NP_055756.1:p.Ile193=
XM_011530003.1:c.789C>T	XP_011528305.1:p.Ile263=
XM_011530004.1:c.780C>T	XP_011528306.1:p.Ile260=
XM_011530005.1:c.789C>T	XP_011528307.1:p.Ile263=
XM_011530006.1:c.630C>T	XP_011528308.1:p.Ile210=
NM_001303256.2:c.765C>T	NP_001290185.1:p.Ile255=
NM_001303257.2:c.765C>T	NP_001290186.1:p.Ile255=
NM_014941.3:c.579C>T	NP_055756.1:p.Ile193=
XM_011530004.2:c.780C>T	XP_011528306.1:p.Ile260=
XM_017028667.2:c.780C>T	XP_016884156.1:p.Ile260=
NM_001303256.3:c.765C>T MANE Select	NP_001290185.1:p.Ile255=