Canonical Allele Identifier: CA10187299
Community Standard Title: NM_001303256.3(MORC2):c.286C>G (p.Gln96Glu)
Gene: MORC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.30949783G>C , CM000684.2:g.30949783G>C GRCh38
NC_000022.10:g.31345769G>C , CM000684.1:g.31345769G>C GRCh37
NC_000022.9:g.29675769G>C NCBI36
NG_046752.1:g.23715C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001303256.3:c.286C>G MANE Select NP_001290185.1:p.Gln96Glu
ENST00000397641.8:c.286C>G MANE Select ENSP00000380763.2:p.Gln96Glu
NM_001303256.1:c.286C>G NP_001290185.1:p.Gln96Glu
NM_001303256.2:c.286C>G NP_001290185.1:p.Gln96Glu
NM_001303257.1:c.286C>G NP_001290186.1:p.Gln96Glu
NM_001303257.2:c.286C>G NP_001290186.1:p.Gln96Glu
NM_014941.2:c.100C>G NP_055756.1:p.Gln34Glu
NM_014941.3:c.100C>G NP_055756.1:p.Gln34Glu
ENST00000215862.8:c.100C>G ENSP00000215862.4:p.Gln34Glu
ENST00000397641.7:c.286C>G ENSP00000380763.2:p.Gln96Glu
ENST00000476152.2:n.408C>G
XM_011530003.1:c.310C>G XP_011528305.1:p.Gln104Glu
XM_011530004.1:c.301C>G XP_011528306.1:p.Gln101Glu
XM_011530004.2:c.301C>G XP_011528306.1:p.Gln101Glu
XM_011530005.1:c.310C>G XP_011528307.1:p.Gln104Glu
XM_011530006.1:c.151C>G XP_011528308.1:p.Gln51Glu
XM_017028667.2:c.301C>G XP_016884156.1:p.Gln101Glu