Canonical Allele Identifier: CA323270057

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30933494G>A , CM000684.2:g.30933494G>A	GRCh38
NC_000022.10:g.31329481G>A , CM000684.1:g.31329481G>A	GRCh37
NC_000022.9:g.29659481G>A	NCBI36
NG_046752.1:g.40004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397641.8:c.2352C>T MANE Select	ENSP00000380763.2:p.Asp784=
ENST00000674576.1:n.3798C>T
ENST00000675317.1:n.773C>T
ENST00000675570.1:c.208C>T
ENST00000675601.1:n.2194C>T
ENST00000675798.1:n.104C>T
ENST00000676215.1:n.3195C>T
ENST00000676263.1:n.597C>T
ENST00000215862.8:c.2166C>T	ENSP00000215862.4:p.Asp722=
ENST00000397641.7:c.2352C>T	ENSP00000380763.2:p.Asp784=
NM_001303256.1:c.2352C>T	NP_001290185.1:p.Asp784=
NM_001303257.1:c.2352C>T	NP_001290186.1:p.Asp784=
NM_014941.2:c.2166C>T	NP_055756.1:p.Asp722=
XM_011530003.1:c.2376C>T	XP_011528305.1:p.Asp792=
XM_011530004.1:c.2367C>T	XP_011528306.1:p.Asp789=
XM_011530005.1:c.2376C>T	XP_011528307.1:p.Asp792=
XM_011530006.1:c.2217C>T	XP_011528308.1:p.Asp739=
NM_001303256.2:c.2352C>T	NP_001290185.1:p.Asp784=
NM_001303257.2:c.2352C>T	NP_001290186.1:p.Asp784=
NM_014941.3:c.2166C>T	NP_055756.1:p.Asp722=
XM_011530004.2:c.2367C>T	XP_011528306.1:p.Asp789=
XM_017028667.2:c.2367C>T	XP_016884156.1:p.Asp789=
NM_001303256.3:c.2352C>T MANE Select	NP_001290185.1:p.Asp784=