Canonical Allele Identifier: CA2740091839

Gene: MIDN

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1254164dup , CM000681.2:g.1254164dup	GRCh38
NC_000019.9:g.1254163dup , CM000681.1:g.1254163dup	GRCh37
NC_000019.8:g.1205163dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001388306.1:c.514-3dup MANE Select	NP_001375235.1:n.514-3dup
ENST00000682408.1:c.514-3dup MANE Select	ENSP00000507955.1:n.514-3dup
NM_001388307.1:c.385-3dup	NP_001375236.1:n.385-3dup
NM_001388474.1:c.385-3dup	NP_001375403.1:n.385-3dup
NM_177401.4:c.385-3dup	NP_796375.3:n.385-3dup
NM_177401.5:c.385-3dup	NP_796375.3:n.385-3dup
ENST00000300952.6:c.385-3dup	ENSP00000300952.2:n.385-3dup
ENST00000300952.7:c.385-3dup	ENSP00000300952.2:n.385-3dup
ENST00000586757.5:c.385-3dup	ENSP00000466895.2:n.385-3dup
ENST00000586843.2:c.281-3dup
ENST00000590136.1:n.400-3dup
ENST00000591302.1:n.453-3dup
ENST00000591446.6:c.385-3dup	ENSP00000467679.1:n.385-3dup
ENST00000591446.7:c.385-3dup	ENSP00000467679.1:n.385-3dup
XM_005259671.2:c.514-3dup	XP_005259728.1:n.514-3dup
XM_005259671.3:c.514-3dup	XP_005259728.1:n.514-3dup
XM_005259672.2:c.514-3dup	XP_005259729.1:n.514-3dup
XM_005259672.3:c.514-3dup	XP_005259729.1:n.514-3dup
XM_024451753.1:c.514-3dup	XP_024307521.1:n.514-3dup
XM_024451754.1:c.385-3dup	XP_024307522.1:n.385-3dup