Canonical Allele Identifier: CA400326772
Community Standard Title: NM_017777.4(MKS1):c.658A>T (p.Lys220Ter)
Gene: MKS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58213856T>A , CM000679.2:g.58213856T>A GRCh38
NC_000017.10:g.56291217T>A , CM000679.1:g.56291217T>A GRCh37
NC_000017.9:g.53646216T>A NCBI36
NG_013032.1:g.10750A>T , LRG_687:g.10750A>T

Transcript Alleles

HGVS Amino-acid Change
NM_017777.4:c.658A>T MANE Select NP_060247.2:p.Lys220Ter
ENST00000393119.7:c.658A>T MANE Select ENSP00000376827.2:p.Lys220Ter
NM_001165927.1:c.628A>T , LRG_687t2:c.628A>T NP_001159399.1:p.Lys210Ter
NM_001321268.1:c.49A>T NP_001308197.1:p.Lys17Ter
NM_001321268.2:c.49A>T NP_001308197.1:p.Lys17Ter
NM_001321269.1:c.658A>T NP_001308198.1:p.Lys220Ter
NM_001321269.2:c.658A>T NP_001308198.1:p.Lys220Ter
NM_001330397.1:c.658A>T NP_001317326.1:p.Lys220Ter
NM_001330397.2:c.658A>T NP_001317326.1:p.Lys220Ter
NM_017777.3:c.658A>T , LRG_687t1:c.658A>T NP_060247.2:p.Lys220Ter
ENST00000313863.10:c.658A>T ENSP00000316631.6:p.Lys220Ter
ENST00000313863.11:c.658A>T ENSP00000316631.6:p.Lys220Ter
ENST00000393119.6:c.658A>T ENSP00000376827.2:p.Lys220Ter
ENST00000393120.6:c.*65A>T ENSP00000376828.2:n.*65A>T
ENST00000537529.6:c.628A>T ENSP00000442096.2:p.Lys210Ter
ENST00000537529.7:c.229A>T ENSP00000442096.3:p.Lys77Ter
ENST00000577824.5:c.135A>T
ENST00000580127.5:c.*277A>T ENSP00000462423.1:n.*277A>T
ENST00000580127.6:c.658A>T ENSP00000462423.2:p.Lys220Ter
ENST00000581761.5:c.*65A>T ENSP00000462129.1:n.*65A>T
ENST00000581761.6:c.658A>T ENSP00000462129.2:p.Lys220Ter
ENST00000585134.2:c.658A>T ENSP00000463826.2:p.Lys220Ter
ENST00000675753.2:c.*277A>T ENSP00000502156.1:n.*277A>T
ENST00000676787.1:c.529A>T ENSP00000503999.1:p.Lys177Ter
ENST00000676975.1:c.523A>T ENSP00000503970.1:n.523A>T
ENST00000677076.1:n.1932A>T
ENST00000677111.1:c.658A>T ENSP00000504282.1:p.Lys220Ter
ENST00000677160.1:n.1932A>T
ENST00000677416.1:n.683A>T
ENST00000677475.1:n.1935A>T
ENST00000677486.1:c.*2A>T ENSP00000503852.1:n.*2A>T
ENST00000677546.1:c.*2A>T ENSP00000504043.1:n.*2A>T
ENST00000677709.1:n.683A>T
ENST00000678011.1:n.683A>T
ENST00000678211.1:n.2707A>T
ENST00000678432.1:c.*277A>T ENSP00000504452.1:n.*277A>T
ENST00000678463.1:c.658A>T ENSP00000502984.1:p.Lys220Ter
ENST00000678481.1:n.459A>T
ENST00000678568.1:c.*65A>T ENSP00000504754.1:n.*65A>T
ENST00000678641.1:c.*2A>T ENSP00000503159.1:n.*2A>T
ENST00000678928.1:n.2285A>T
ENST00000679081.1:n.2674A>T
XM_005257483.3:c.658A>T XP_005257540.1:p.Lys220Ter
XM_005257485.3:c.229A>T XP_005257542.1:p.Lys77Ter
XM_005257485.4:c.229A>T XP_005257542.1:p.Lys77Ter
XM_005257486.3:c.49A>T XP_005257543.1:p.Lys17Ter
XM_006721965.2:c.49A>T XP_006722028.1:p.Lys17Ter
XM_006721965.3:c.49A>T XP_006722028.1:p.Lys17Ter
XM_011524957.1:c.667A>T XP_011523259.1:p.Lys223Ter
XM_011524957.2:c.667A>T XP_011523259.1:p.Lys223Ter
XM_011524958.1:c.667A>T XP_011523260.1:p.Lys223Ter
XM_011524958.2:c.667A>T XP_011523260.1:p.Lys223Ter
XM_011524959.1:c.667A>T XP_011523261.1:p.Lys223Ter
XM_011524959.2:c.667A>T XP_011523261.1:p.Lys223Ter
XM_011524960.1:c.667A>T XP_011523262.1:p.Lys223Ter
XM_011524960.2:c.667A>T XP_011523262.1:p.Lys223Ter
XM_017024804.2:c.658A>T XP_016880293.1:p.Lys220Ter
XM_017024805.1:c.229A>T XP_016880294.1:p.Lys77Ter
XR_002958042.1:n.712A>T
XR_934494.1:n.715A>T