Canonical Allele Identifier: CA2267604878

Gene: MKS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58213034G= , CM000679.2:g.58213034G=	GRCh38
NC_000017.10:g.56290395G= , CM000679.1:g.56290395G=	GRCh37
NC_000017.9:g.53645394G=	NCBI36
NG_013032.1:g.11572C= , LRG_687:g.11572C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313863.11:c.806C=	ENSP00000316631.6:p.Ser269=
ENST00000393119.7:c.806C= MANE Select	ENSP00000376827.2:p.Ser269=
ENST00000537529.7:c.377C=	ENSP00000442096.3:p.Ser126=
ENST00000580127.6:c.806C=	ENSP00000462423.2:p.Ser269=
ENST00000581761.6:c.806C=	ENSP00000462129.2:p.Ser269=
ENST00000585134.2:c.806C=	ENSP00000463826.2:p.Ser269=
ENST00000675753.2:c.*425C=	ENSP00000502156.1:n.*425C=
ENST00000676787.1:c.677C=	ENSP00000503999.1:p.Ser226=
ENST00000676975.1:c.671C=	ENSP00000503970.1:n.671C=
ENST00000677076.1:n.2080C=
ENST00000677111.1:c.806C=	ENSP00000504282.1:p.Ser269=
ENST00000677160.1:n.2080C=
ENST00000677416.1:n.831C=
ENST00000677475.1:n.2757C=
ENST00000677486.1:c.*150C=	ENSP00000503852.1:n.*150C=
ENST00000677546.1:c.*150C=	ENSP00000504043.1:n.*150C=
ENST00000677709.1:n.831C=
ENST00000678011.1:n.831C=
ENST00000678211.1:n.2855C=
ENST00000678432.1:c.*425C=	ENSP00000504452.1:n.*425C=
ENST00000678463.1:c.806C=	ENSP00000502984.1:p.Ser269=
ENST00000678481.1:n.607C=
ENST00000678568.1:c.*213C=	ENSP00000504754.1:n.*213C=
ENST00000678641.1:c.*150C=	ENSP00000503159.1:n.*150C=
ENST00000678928.1:n.2433C=
ENST00000679081.1:n.2822C=
ENST00000313863.10:c.806C=	ENSP00000316631.6:p.Ser269=
ENST00000393119.6:c.806C=	ENSP00000376827.2:p.Ser269=
ENST00000393120.6:c.*213C=	ENSP00000376828.2:n.*213C=
ENST00000537529.6:c.776C=	ENSP00000442096.2:p.Ser259=
ENST00000577824.5:c.283C=
ENST00000581761.5:c.*213C=	ENSP00000462129.1:n.*213C=
ENST00000585134.1:c.29C=	ENSP00000463826.1:p.Ser10=
NM_001165927.1:c.776C= , LRG_687t2:c.776C=	NP_001159399.1:p.Ser259=
NM_017777.3:c.806C= , LRG_687t1:c.806C=	NP_060247.2:p.Ser269=
XM_005257483.3:c.806C=	XP_005257540.1:p.Ser269=
XM_005257485.3:c.377C=	XP_005257542.1:p.Ser126=
XM_005257486.3:c.197C=	XP_005257543.1:p.Ser66=
XM_006721965.2:c.197C=	XP_006722028.1:p.Ser66=
XM_011524957.1:c.815C=	XP_011523259.1:p.Ser272=
XM_011524958.1:c.815C=	XP_011523260.1:p.Ser272=
XM_011524959.1:c.815C=	XP_011523261.1:p.Ser272=
XM_011524960.1:c.815C=	XP_011523262.1:p.Ser272=
XR_934494.1:n.863C=
NM_001321268.1:c.197C=	NP_001308197.1:p.Ser66=
NM_001321269.1:c.806C=	NP_001308198.1:p.Ser269=
NM_001330397.1:c.806C=	NP_001317326.1:p.Ser269=
XM_005257485.4:c.377C=	XP_005257542.1:p.Ser126=
XM_006721965.3:c.197C=	XP_006722028.1:p.Ser66=
XM_011524957.2:c.815C=	XP_011523259.1:p.Ser272=
XM_011524958.2:c.815C=	XP_011523260.1:p.Ser272=
XM_011524959.2:c.815C=	XP_011523261.1:p.Ser272=
XM_011524960.2:c.815C=	XP_011523262.1:p.Ser272=
XM_017024804.2:c.806C=	XP_016880293.1:p.Ser269=
XM_017024805.1:c.377C=	XP_016880294.1:p.Ser126=
XR_002958042.1:n.860C=
NM_001321268.2:c.197C=	NP_001308197.1:p.Ser66=
NM_001321269.2:c.806C=	NP_001308198.1:p.Ser269=
NM_001330397.2:c.806C=	NP_001317326.1:p.Ser269=
NM_017777.4:c.806C= MANE Select	NP_060247.2:p.Ser269=