Canonical Allele Identifier: CA9040709

Gene: MIDN

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1254464A>G , CM000681.2:g.1254464A>G	GRCh38
NC_000019.9:g.1254463A>G , CM000681.1:g.1254463A>G	GRCh37
NC_000019.8:g.1205463A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001388306.1:c.811A>G MANE Select	NP_001375235.1:p.Thr271Ala
ENST00000682408.1:c.811A>G MANE Select	ENSP00000507955.1:p.Thr271Ala
NM_001388307.1:c.682A>G	NP_001375236.1:p.Thr228Ala
NM_001388474.1:c.682A>G	NP_001375403.1:p.Thr228Ala
NM_177401.4:c.682A>G	NP_796375.3:p.Thr228Ala
NM_177401.5:c.682A>G	NP_796375.3:p.Thr228Ala
ENST00000300952.6:c.682A>G	ENSP00000300952.2:p.Thr228Ala
ENST00000300952.7:c.682A>G	ENSP00000300952.2:p.Thr228Ala
ENST00000591446.6:c.682A>G	ENSP00000467679.1:p.Thr228Ala
ENST00000591446.7:c.682A>G	ENSP00000467679.1:p.Thr228Ala
XM_005259671.2:c.811A>G	XP_005259728.1:p.Thr271Ala
XM_005259671.3:c.811A>G	XP_005259728.1:p.Thr271Ala
XM_005259672.2:c.811A>G	XP_005259729.1:p.Thr271Ala
XM_005259672.3:c.811A>G	XP_005259729.1:p.Thr271Ala
XM_024451753.1:c.811A>G	XP_024307521.1:p.Thr271Ala
XM_024451754.1:c.682A>G	XP_024307522.1:p.Thr228Ala