Canonical Allele Identifier: CA10187267

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30946362A>G , CM000684.2:g.30946362A>G	GRCh38
NC_000022.10:g.31342349A>G , CM000684.1:g.31342349A>G	GRCh37
NC_000022.9:g.29672349A>G	NCBI36
NG_046752.1:g.27136T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001303256.3:c.405T>C MANE Select	NP_001290185.1:p.His135=
ENST00000397641.8:c.405T>C MANE Select	ENSP00000380763.2:p.His135=
NM_001303256.1:c.405T>C	NP_001290185.1:p.His135=
NM_001303256.2:c.405T>C	NP_001290185.1:p.His135=
NM_001303257.1:c.405T>C	NP_001290186.1:p.His135=
NM_001303257.2:c.405T>C	NP_001290186.1:p.His135=
NM_014941.2:c.219T>C	NP_055756.1:p.His73=
NM_014941.3:c.219T>C	NP_055756.1:p.His73=
ENST00000215862.8:c.219T>C	ENSP00000215862.4:p.His73=
ENST00000397641.7:c.405T>C	ENSP00000380763.2:p.His135=
ENST00000476152.2:n.527T>C
ENST00000675601.1:n.247T>C
XM_011530003.1:c.429T>C	XP_011528305.1:p.His143=
XM_011530004.1:c.420T>C	XP_011528306.1:p.His140=
XM_011530004.2:c.420T>C	XP_011528306.1:p.His140=
XM_011530005.1:c.429T>C	XP_011528307.1:p.His143=
XM_011530006.1:c.270T>C	XP_011528308.1:p.His90=
XM_017028667.2:c.420T>C	XP_016884156.1:p.His140=