Canonical Allele Identifier: CA2267604862
Gene: MKS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58213005G= , CM000679.2:g.58213005G= GRCh38
NC_000017.10:g.56290366G= , CM000679.1:g.56290366G= GRCh37
NC_000017.9:g.53645365G= NCBI36
NG_013032.1:g.11601C= , LRG_687:g.11601C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313863.11:c.835C= ENSP00000316631.6:p.Arg279=
ENST00000393119.7:c.835C= MANE Select ENSP00000376827.2:p.Arg279=
ENST00000537529.7:c.406C= ENSP00000442096.3:p.Arg136=
ENST00000580127.6:c.835C= ENSP00000462423.2:p.Arg279=
ENST00000581761.6:c.835C= ENSP00000462129.2:p.Arg279=
ENST00000585134.2:c.835C= ENSP00000463826.2:p.Arg279=
ENST00000675753.2:c.*454C= ENSP00000502156.1:n.*454C=
ENST00000676787.1:c.706C= ENSP00000503999.1:p.Arg236=
ENST00000676975.1:c.700C= ENSP00000503970.1:n.700C=
ENST00000677076.1:n.2109C=
ENST00000677111.1:c.835C= ENSP00000504282.1:p.Arg279=
ENST00000677160.1:n.2109C=
ENST00000677416.1:n.860C=
ENST00000677475.1:n.2786C=
ENST00000677486.1:c.*179C= ENSP00000503852.1:n.*179C=
ENST00000677546.1:c.*179C= ENSP00000504043.1:n.*179C=
ENST00000677709.1:n.860C=
ENST00000678011.1:n.860C=
ENST00000678211.1:n.2884C=
ENST00000678432.1:c.*454C= ENSP00000504452.1:n.*454C=
ENST00000678463.1:c.835C= ENSP00000502984.1:p.Arg279=
ENST00000678481.1:n.636C=
ENST00000678568.1:c.*242C= ENSP00000504754.1:n.*242C=
ENST00000678641.1:c.*179C= ENSP00000503159.1:n.*179C=
ENST00000678928.1:n.2462C=
ENST00000679081.1:n.2851C=
ENST00000313863.10:c.835C= ENSP00000316631.6:p.Arg279=
ENST00000393119.6:c.835C= ENSP00000376827.2:p.Arg279=
ENST00000393120.6:c.*242C= ENSP00000376828.2:n.*242C=
ENST00000537529.6:c.805C= ENSP00000442096.2:p.Arg269=
ENST00000577824.5:c.312C=
ENST00000581761.5:c.*242C= ENSP00000462129.1:n.*242C=
ENST00000585134.1:c.58C= ENSP00000463826.1:p.Arg20=
NM_001165927.1:c.805C= , LRG_687t2:c.805C= NP_001159399.1:p.Arg269=
NM_017777.3:c.835C= , LRG_687t1:c.835C= NP_060247.2:p.Arg279=
XM_005257483.3:c.835C= XP_005257540.1:p.Arg279=
XM_005257485.3:c.406C= XP_005257542.1:p.Arg136=
XM_005257486.3:c.226C= XP_005257543.1:p.Arg76=
XM_006721965.2:c.226C= XP_006722028.1:p.Arg76=
XM_011524957.1:c.844C= XP_011523259.1:p.Arg282=
XM_011524958.1:c.844C= XP_011523260.1:p.Arg282=
XM_011524959.1:c.844C= XP_011523261.1:p.Arg282=
XM_011524960.1:c.844C= XP_011523262.1:p.Arg282=
XR_934494.1:n.892C=
NM_001321268.1:c.226C= NP_001308197.1:p.Arg76=
NM_001321269.1:c.835C= NP_001308198.1:p.Arg279=
NM_001330397.1:c.835C= NP_001317326.1:p.Arg279=
XM_005257485.4:c.406C= XP_005257542.1:p.Arg136=
XM_006721965.3:c.226C= XP_006722028.1:p.Arg76=
XM_011524957.2:c.844C= XP_011523259.1:p.Arg282=
XM_011524958.2:c.844C= XP_011523260.1:p.Arg282=
XM_011524959.2:c.844C= XP_011523261.1:p.Arg282=
XM_011524960.2:c.844C= XP_011523262.1:p.Arg282=
XM_017024804.2:c.835C= XP_016880293.1:p.Arg279=
XM_017024805.1:c.406C= XP_016880294.1:p.Arg136=
XR_002958042.1:n.889C=
NM_001321268.2:c.226C= NP_001308197.1:p.Arg76=
NM_001321269.2:c.835C= NP_001308198.1:p.Arg279=
NM_001330397.2:c.835C= NP_001317326.1:p.Arg279=
NM_017777.4:c.835C= MANE Select NP_060247.2:p.Arg279=