Canonical Allele Identifier: CA275425
Gene: MID1 HGNC NCBI

Linked Data

ClinVar Variation Id: 198721
ClinVar RCV Id: RCV000180149
dbSNP Id: rs797044786

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.10459649_10459652dup , CM000685.2:g.10459649_10459652dup GRCh38
NC_000023.10:g.10427689_10427692dup , CM000685.1:g.10427689_10427692dup GRCh37
NC_000023.9:g.10387689_10387692dup NCBI36
NG_008197.1:g.379042_379045dup
NG_008197.2:g.379042_379045dup

Transcript Alleles

HGVS Amino-acid change
ENST00000413894.6:c.1444_1447dup ENSP00000391154.2:p.Ser483LysfsTer6
ENST00000689773.1:c.1330_1333dup ENSP00000509925.1:p.Ser445LysfsTer6
ENST00000690004.1:c.1330_1333dup ENSP00000509730.1:p.Ser445LysfsTer6
ENST00000691943.1:c.1336_1339dup ENSP00000508663.1:p.Ser447LysfsTer6
ENST00000317552.9:c.1444_1447dup MANE Select ENSP00000312678.4:p.Ser483LysfsTer6
ENST00000674917.1:c.577_580dup ENSP00000502171.1:p.Ser194LysfsTer6
ENST00000675073.1:c.1597_1600dup ENSP00000501707.1:p.Ser534LysfsTer6
ENST00000317552.8:c.1444_1447dup ENSP00000312678.4:p.Ser483LysfsTer6
ENST00000380779.5:c.1444_1447dup ENSP00000370156.1:p.Ser483LysfsTer6
ENST00000380780.5:c.1444_1447dup ENSP00000370157.1:p.Ser483LysfsTer6
ENST00000380782.6:c.1444_1447dup ENSP00000370159.1:p.Ser483LysfsTer6
ENST00000380785.5:c.1444_1447dup ENSP00000370162.1:p.Ser483LysfsTer6
ENST00000380787.5:c.1444_1447dup ENSP00000370164.1:p.Ser483LysfsTer6
ENST00000413894.5:c.1444_1447dup ENSP00000391154.1:p.Ser483LysfsTer?
ENST00000453318.6:c.1444_1447dup ENSP00000414521.2:p.Ser483LysfsTer6
ENST00000479925.1:n.394_397dup
NM_000381.3:c.1444_1447dup NP_000372.1:p.Ser483LysfsTer6
NM_001098624.2:c.1444_1447dup NP_001092094.1:p.Ser483LysfsTer6
NM_001193277.1:c.1444_1447dup NP_001180206.1:p.Ser483LysfsTer6
NM_033289.1:c.1330_1333dup NP_150631.1:p.Ser445LysfsTer6
NM_033290.3:c.1444_1447dup NP_150632.1:p.Ser483LysfsTer6
XM_005274536.1:c.1597_1600dup XP_005274593.1:p.Ser534LysfsTer6
XM_005274537.1:c.1597_1600dup XP_005274594.1:p.Ser534LysfsTer6
XM_006724492.2:c.1597_1600dup XP_006724555.1:p.Ser534LysfsTer6
XM_006724493.2:c.1483_1486dup XP_006724556.1:p.Ser496LysfsTer6
XM_011545525.1:c.1597_1600dup XP_011543827.1:p.Ser534LysfsTer6
XM_011545526.1:c.1597_1600dup XP_011543828.1:p.Ser534LysfsTer6
XM_011545527.1:c.1597_1600dup XP_011543829.1:p.Ser534LysfsTer6
NM_001347733.1:c.1444_1447dup NP_001334662.1:p.Ser483LysfsTer6
NM_000381.4:c.1444_1447dup MANE Select NP_000372.1:p.Ser483LysfsTer6
NM_001347733.2:c.1444_1447dup NP_001334662.1:p.Ser483LysfsTer6
NM_033289.2:c.1330_1333dup NP_150631.1:p.Ser445LysfsTer6
NM_033290.4:c.1444_1447dup NP_150632.1:p.Ser483LysfsTer6