Canonical Allele Identifier: CA326621490

Gene: MID1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.10469363dup , CM000685.2:g.10469363dup	GRCh38
NC_000023.10:g.10437403dup , CM000685.1:g.10437403dup	GRCh37
NC_000023.9:g.10397403dup	NCBI36
NG_008197.1:g.369329dup
NG_008197.2:g.369329dup

Transcript Alleles

HGVS	Amino-acid Change
NM_000381.4:c.1285+335dup MANE Select	NP_000372.1:n.1285+335dup
ENST00000317552.9:c.1285+335dup MANE Select	ENSP00000312678.4:n.1285+335dup
NM_000381.3:c.1285+335dup	NP_000372.1:n.1285+335dup
NM_001098624.2:c.1285+335dup	NP_001092094.1:n.1285+335dup
NM_001193277.1:c.1285+335dup	NP_001180206.1:n.1285+335dup
NM_001193278.1:c.*150dup	NP_001180207.1:n.*150dup
NM_001193279.1:c.*150dup	NP_001180208.1:n.*150dup
NM_001193280.1:c.*150dup	NP_001180209.1:n.*150dup
NM_001347733.1:c.1285+335dup	NP_001334662.1:n.1285+335dup
NM_001347733.2:c.1285+335dup	NP_001334662.1:n.1285+335dup
NM_033289.1:c.1171+335dup	NP_150631.1:n.1171+335dup
NM_033289.2:c.1171+335dup	NP_150631.1:n.1171+335dup
NM_033290.3:c.1285+335dup	NP_150632.1:n.1285+335dup
NM_033290.4:c.1285+335dup	NP_150632.1:n.1285+335dup
ENST00000317552.8:c.1285+335dup	ENSP00000312678.4:n.1285+335dup
ENST00000380779.5:c.1285+335dup	ENSP00000370156.1:n.1285+335dup
ENST00000380780.5:c.1285+335dup	ENSP00000370157.1:n.1285+335dup
ENST00000380782.6:c.1285+335dup	ENSP00000370159.1:n.1285+335dup
ENST00000380785.5:c.1285+335dup	ENSP00000370162.1:n.1285+335dup
ENST00000380787.5:c.1285+335dup	ENSP00000370164.1:n.1285+335dup
ENST00000413894.5:c.1285+335dup	ENSP00000391154.1:n.1285+335dup
ENST00000413894.6:c.1285+335dup	ENSP00000391154.2:n.1285+335dup
ENST00000453318.6:c.1285+335dup	ENSP00000414521.2:n.1285+335dup
ENST00000616003.4:c.*150dup	ENSP00000484712.1:n.*150dup
ENST00000616003.5:c.*150dup	ENSP00000484712.1:n.*150dup
ENST00000674917.1:c.418+335dup	ENSP00000502171.1:n.418+335dup
ENST00000675073.1:c.1438+335dup	ENSP00000501707.1:n.1438+335dup
ENST00000687008.1:c.1620dup	ENSP00000508734.1:n.1620dup
ENST00000689773.1:c.1171+335dup	ENSP00000509925.1:n.1171+335dup
ENST00000690004.1:c.1171+335dup	ENSP00000509730.1:n.1171+335dup
ENST00000691913.1:n.1018dup
ENST00000691943.1:c.1177+335dup	ENSP00000508663.1:n.1177+335dup
XM_005274536.1:c.1438+335dup	XP_005274593.1:n.1438+335dup
XM_005274537.1:c.1438+335dup	XP_005274594.1:n.1438+335dup
XM_005274538.3:c.*150dup	XP_005274595.1:n.*150dup
XM_006724492.2:c.1438+335dup	XP_006724555.1:n.1438+335dup
XM_006724493.2:c.1324+335dup	XP_006724556.1:n.1324+335dup
XM_011545525.1:c.1438+335dup	XP_011543827.1:n.1438+335dup
XM_011545526.1:c.1438+335dup	XP_011543828.1:n.1438+335dup
XM_011545527.1:c.1438+335dup	XP_011543829.1:n.1438+335dup