Canonical Allele Identifier: CA2267606132
Gene: MKS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58216126T= , CM000679.2:g.58216126T= GRCh38
NC_000017.10:g.56293487T= , CM000679.1:g.56293487T= GRCh37
NC_000017.9:g.53648486T= NCBI36
NG_013032.1:g.8480A= , LRG_687:g.8480A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313863.11:c.379A= ENSP00000316631.6:p.Thr127=
ENST00000393119.7:c.379A= MANE Select ENSP00000376827.2:p.Thr127=
ENST00000537529.7:c.-51A= ENSP00000442096.3:n.-51A=
ENST00000580127.6:c.379A= ENSP00000462423.2:p.Thr127=
ENST00000581180.2:c.379A= ENSP00000502288.1:p.Thr127=
ENST00000581761.6:c.379A= ENSP00000462129.2:p.Thr127=
ENST00000585134.2:c.379A= ENSP00000463826.2:p.Thr127=
ENST00000675753.2:c.379A= ENSP00000502156.1:p.Thr127=
ENST00000676787.1:c.379A= ENSP00000503999.1:p.Thr127=
ENST00000676975.1:c.40A= ENSP00000503970.1:p.Thr14=
ENST00000677076.1:n.404A=
ENST00000677111.1:c.379A= ENSP00000504282.1:p.Thr127=
ENST00000677160.1:n.404A=
ENST00000677416.1:n.404A=
ENST00000677475.1:n.407A=
ENST00000677486.1:c.261+540A= ENSP00000503852.1:n.261+540A=
ENST00000677546.1:c.379A= ENSP00000504043.1:p.Thr127=
ENST00000677709.1:n.404A=
ENST00000677791.1:n.407A=
ENST00000678011.1:n.404A=
ENST00000678211.1:n.826A=
ENST00000678432.1:c.379A= ENSP00000504452.1:p.Thr127=
ENST00000678463.1:c.379A= ENSP00000502984.1:p.Thr127=
ENST00000678481.1:n.407A=
ENST00000678568.1:c.191-1288A= ENSP00000504754.1:n.191-1288A=
ENST00000678641.1:c.379A= ENSP00000503159.1:p.Thr127=
ENST00000678928.1:n.404A=
ENST00000679081.1:n.404A=
ENST00000313863.10:c.379A= ENSP00000316631.6:p.Thr127=
ENST00000393119.6:c.379A= ENSP00000376827.2:p.Thr127=
ENST00000393120.6:c.379A= ENSP00000376828.2:p.Thr127=
ENST00000537529.6:c.349A= ENSP00000442096.2:p.Thr117=
ENST00000578789.1:c.*122A= ENSP00000462411.1:n.*122A=
ENST00000580127.5:c.379A= ENSP00000462423.1:p.Thr127=
ENST00000581180.1:n.379A=
ENST00000581761.5:c.191-1288A= ENSP00000462129.1:n.191-1288A=
NM_001165927.1:c.349A= , LRG_687t2:c.349A= NP_001159399.1:p.Thr117=
NM_017777.3:c.379A= , LRG_687t1:c.379A= NP_060247.2:p.Thr127=
XM_005257483.3:c.379A= XP_005257540.1:p.Thr127=
XM_005257485.3:c.-111A= XP_005257542.1:n.-111A=
XM_005257486.3:c.-133A= XP_005257543.1:n.-133A=
XM_006721965.2:c.-133A= XP_006722028.1:n.-133A=
XM_011524957.1:c.388A= XP_011523259.1:p.Thr130=
XM_011524958.1:c.388A= XP_011523260.1:p.Thr130=
XM_011524959.1:c.388A= XP_011523261.1:p.Thr130=
XM_011524960.1:c.388A= XP_011523262.1:p.Thr130=
XR_934494.1:n.436A=
NM_001321268.1:c.-133A= NP_001308197.1:n.-133A=
NM_001321269.1:c.379A= NP_001308198.1:p.Thr127=
NM_001330397.1:c.379A= NP_001317326.1:p.Thr127=
XM_005257485.4:c.-111A= XP_005257542.1:n.-111A=
XM_006721965.3:c.-133A= XP_006722028.1:n.-133A=
XM_011524957.2:c.388A= XP_011523259.1:p.Thr130=
XM_011524958.2:c.388A= XP_011523260.1:p.Thr130=
XM_011524959.2:c.388A= XP_011523261.1:p.Thr130=
XM_011524960.2:c.388A= XP_011523262.1:p.Thr130=
XM_017024804.2:c.379A= XP_016880293.1:p.Thr127=
XM_017024805.1:c.-111A= XP_016880294.1:n.-111A=
XR_002958042.1:n.433A=
NM_001321268.2:c.-133A= NP_001308197.1:n.-133A=
NM_001321269.2:c.379A= NP_001308198.1:p.Thr127=
NM_001330397.2:c.379A= NP_001317326.1:p.Thr127=
NM_017777.4:c.379A= MANE Select NP_060247.2:p.Thr127=