Canonical Allele Identifier: CA501032127

Gene: MKS1

Linked Data

• MyVariant Identifiers: chr17:g.56290364C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58213003C>G , CM000679.2:g.58213003C>G	GRCh38
NC_000017.10:g.56290364C>G , CM000679.1:g.56290364C>G	GRCh37
NC_000017.9:g.53645363C>G	NCBI36
NG_013032.1:g.11603G>C , LRG_687:g.11603G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313863.11:c.837G>C	ENSP00000316631.6:p.Arg279=
ENST00000393119.7:c.837G>C MANE Select	ENSP00000376827.2:p.Arg279=
ENST00000537529.7:c.408G>C	ENSP00000442096.3:p.Arg136=
ENST00000580127.6:c.837G>C	ENSP00000462423.2:p.Arg279=
ENST00000581761.6:c.837G>C	ENSP00000462129.2:p.Arg279=
ENST00000585134.2:c.837G>C	ENSP00000463826.2:p.Arg279=
ENST00000675753.2:c.*456G>C	ENSP00000502156.1:n.*456G>C
ENST00000676787.1:c.708G>C	ENSP00000503999.1:p.Arg236=
ENST00000676975.1:c.702G>C	ENSP00000503970.1:n.702G>C
ENST00000677076.1:n.2111G>C
ENST00000677111.1:c.837G>C	ENSP00000504282.1:p.Arg279=
ENST00000677160.1:n.2111G>C
ENST00000677416.1:n.862G>C
ENST00000677475.1:n.2788G>C
ENST00000677486.1:c.*181G>C	ENSP00000503852.1:n.*181G>C
ENST00000677546.1:c.*181G>C	ENSP00000504043.1:n.*181G>C
ENST00000677709.1:n.862G>C
ENST00000678011.1:n.862G>C
ENST00000678211.1:n.2886G>C
ENST00000678432.1:c.*456G>C	ENSP00000504452.1:n.*456G>C
ENST00000678463.1:c.837G>C	ENSP00000502984.1:p.Arg279=
ENST00000678481.1:n.638G>C
ENST00000678568.1:c.*244G>C	ENSP00000504754.1:n.*244G>C
ENST00000678641.1:c.*181G>C	ENSP00000503159.1:n.*181G>C
ENST00000678928.1:n.2464G>C
ENST00000679081.1:n.2853G>C
ENST00000313863.10:c.837G>C	ENSP00000316631.6:p.Arg279=
ENST00000393119.6:c.837G>C	ENSP00000376827.2:p.Arg279=
ENST00000393120.6:c.*244G>C	ENSP00000376828.2:n.*244G>C
ENST00000537529.6:c.807G>C	ENSP00000442096.2:p.Arg269=
ENST00000577824.5:c.314G>C
ENST00000581761.5:c.*244G>C	ENSP00000462129.1:n.*244G>C
ENST00000585134.1:c.60G>C	ENSP00000463826.1:p.Arg20=
NM_001165927.1:c.807G>C , LRG_687t2:c.807G>C	NP_001159399.1:p.Arg269=
NM_017777.3:c.837G>C , LRG_687t1:c.837G>C	NP_060247.2:p.Arg279=
XM_005257483.3:c.837G>C	XP_005257540.1:p.Arg279=
XM_005257485.3:c.408G>C	XP_005257542.1:p.Arg136=
XM_005257486.3:c.228G>C	XP_005257543.1:p.Arg76=
XM_006721965.2:c.228G>C	XP_006722028.1:p.Arg76=
XM_011524957.1:c.846G>C	XP_011523259.1:p.Arg282=
XM_011524958.1:c.846G>C	XP_011523260.1:p.Arg282=
XM_011524959.1:c.846G>C	XP_011523261.1:p.Arg282=
XM_011524960.1:c.846G>C	XP_011523262.1:p.Arg282=
XR_934494.1:n.894G>C
NM_001321268.1:c.228G>C	NP_001308197.1:p.Arg76=
NM_001321269.1:c.837G>C	NP_001308198.1:p.Arg279=
NM_001330397.1:c.837G>C	NP_001317326.1:p.Arg279=
XM_005257485.4:c.408G>C	XP_005257542.1:p.Arg136=
XM_006721965.3:c.228G>C	XP_006722028.1:p.Arg76=
XM_011524957.2:c.846G>C	XP_011523259.1:p.Arg282=
XM_011524958.2:c.846G>C	XP_011523260.1:p.Arg282=
XM_011524959.2:c.846G>C	XP_011523261.1:p.Arg282=
XM_011524960.2:c.846G>C	XP_011523262.1:p.Arg282=
XM_017024804.2:c.837G>C	XP_016880293.1:p.Arg279=
XM_017024805.1:c.408G>C	XP_016880294.1:p.Arg136=
XR_002958042.1:n.891G>C
NM_001321268.2:c.228G>C	NP_001308197.1:p.Arg76=
NM_001321269.2:c.837G>C	NP_001308198.1:p.Arg279=
NM_001330397.2:c.837G>C	NP_001317326.1:p.Arg279=
NM_017777.4:c.837G>C MANE Select	NP_060247.2:p.Arg279=