Canonical Allele Identifier: CA10187307

Gene: MORC2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30949850G>A , CM000684.2:g.30949850G>A	GRCh38
NC_000022.10:g.31345836G>A , CM000684.1:g.31345836G>A	GRCh37
NC_000022.9:g.29675836G>A	NCBI36
NG_046752.1:g.23648C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397641.8:c.227-8C>T MANE Select	ENSP00000380763.2:n.227-8C>T
ENST00000215862.8:c.41-8C>T	ENSP00000215862.4:n.41-8C>T
ENST00000397641.7:c.227-8C>T	ENSP00000380763.2:n.227-8C>T
ENST00000476152.2:n.349-8C>T
NM_001303256.1:c.227-8C>T	NP_001290185.1:n.227-8C>T
NM_001303257.1:c.227-8C>T	NP_001290186.1:n.227-8C>T
NM_014941.2:c.41-8C>T	NP_055756.1:n.41-8C>T
XM_011530003.1:c.251-8C>T	XP_011528305.1:n.251-8C>T
XM_011530004.1:c.242-8C>T	XP_011528306.1:n.242-8C>T
XM_011530005.1:c.251-8C>T	XP_011528307.1:n.251-8C>T
XM_011530006.1:c.92-8C>T	XP_011528308.1:n.92-8C>T
NM_001303256.2:c.227-8C>T	NP_001290185.1:n.227-8C>T
NM_001303257.2:c.227-8C>T	NP_001290186.1:n.227-8C>T
NM_014941.3:c.41-8C>T	NP_055756.1:n.41-8C>T
XM_011530004.2:c.242-8C>T	XP_011528306.1:n.242-8C>T
XM_017028667.2:c.242-8C>T	XP_016884156.1:n.242-8C>T
NM_001303256.3:c.227-8C>T MANE Select	NP_001290185.1:n.227-8C>T