Canonical Allele Identifier: CA400326504

Gene: MKS1

Linked Data

• MyVariant Identifiers: chr17:g.56290427C>G (hg19) ; chr17:g.58213066C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58213066C>G , CM000679.2:g.58213066C>G	GRCh38
NC_000017.10:g.56290427C>G , CM000679.1:g.56290427C>G	GRCh37
NC_000017.9:g.53645426C>G	NCBI36
NG_013032.1:g.11540G>C , LRG_687:g.11540G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313863.11:c.774G>C	ENSP00000316631.6:p.Gln258His
ENST00000393119.7:c.774G>C MANE Select	ENSP00000376827.2:p.Gln258His
ENST00000537529.7:c.345G>C	ENSP00000442096.3:p.Gln115His
ENST00000580127.6:c.774G>C	ENSP00000462423.2:p.Gln258His
ENST00000581761.6:c.774G>C	ENSP00000462129.2:p.Gln258His
ENST00000585134.2:c.774G>C	ENSP00000463826.2:p.Gln258His
ENST00000675753.2:c.*393G>C	ENSP00000502156.1:n.*393G>C
ENST00000676787.1:c.645G>C	ENSP00000503999.1:p.Gln215His
ENST00000676975.1:c.639G>C	ENSP00000503970.1:n.639G>C
ENST00000677076.1:n.2048G>C
ENST00000677111.1:c.774G>C	ENSP00000504282.1:p.Gln258His
ENST00000677160.1:n.2048G>C
ENST00000677416.1:n.799G>C
ENST00000677475.1:n.2725G>C
ENST00000677486.1:c.*118G>C	ENSP00000503852.1:n.*118G>C
ENST00000677546.1:c.*118G>C	ENSP00000504043.1:n.*118G>C
ENST00000677709.1:n.799G>C
ENST00000678011.1:n.799G>C
ENST00000678211.1:n.2823G>C
ENST00000678432.1:c.*393G>C	ENSP00000504452.1:n.*393G>C
ENST00000678463.1:c.774G>C	ENSP00000502984.1:p.Gln258His
ENST00000678481.1:n.575G>C
ENST00000678568.1:c.*181G>C	ENSP00000504754.1:n.*181G>C
ENST00000678641.1:c.*118G>C	ENSP00000503159.1:n.*118G>C
ENST00000678928.1:n.2401G>C
ENST00000679081.1:n.2790G>C
ENST00000313863.10:c.774G>C	ENSP00000316631.6:p.Gln258His
ENST00000393119.6:c.774G>C	ENSP00000376827.2:p.Gln258His
ENST00000393120.6:c.*181G>C	ENSP00000376828.2:n.*181G>C
ENST00000537529.6:c.744G>C	ENSP00000442096.2:p.Gln248His
ENST00000577824.5:c.251G>C
ENST00000581761.5:c.*181G>C	ENSP00000462129.1:n.*181G>C
NM_001165927.1:c.744G>C , LRG_687t2:c.744G>C	NP_001159399.1:p.Gln248His
NM_017777.3:c.774G>C , LRG_687t1:c.774G>C	NP_060247.2:p.Gln258His
XM_005257483.3:c.774G>C	XP_005257540.1:p.Gln258His
XM_005257485.3:c.345G>C	XP_005257542.1:p.Gln115His
XM_005257486.3:c.165G>C	XP_005257543.1:p.Gln55His
XM_006721965.2:c.165G>C	XP_006722028.1:p.Gln55His
XM_011524957.1:c.783G>C	XP_011523259.1:p.Gln261His
XM_011524958.1:c.783G>C	XP_011523260.1:p.Gln261His
XM_011524959.1:c.783G>C	XP_011523261.1:p.Gln261His
XM_011524960.1:c.783G>C	XP_011523262.1:p.Gln261His
XR_934494.1:n.831G>C
NM_001321268.1:c.165G>C	NP_001308197.1:p.Gln55His
NM_001321269.1:c.774G>C	NP_001308198.1:p.Gln258His
NM_001330397.1:c.774G>C	NP_001317326.1:p.Gln258His
XM_005257485.4:c.345G>C	XP_005257542.1:p.Gln115His
XM_006721965.3:c.165G>C	XP_006722028.1:p.Gln55His
XM_011524957.2:c.783G>C	XP_011523259.1:p.Gln261His
XM_011524958.2:c.783G>C	XP_011523260.1:p.Gln261His
XM_011524959.2:c.783G>C	XP_011523261.1:p.Gln261His
XM_011524960.2:c.783G>C	XP_011523262.1:p.Gln261His
XM_017024804.2:c.774G>C	XP_016880293.1:p.Gln258His
XM_017024805.1:c.345G>C	XP_016880294.1:p.Gln115His
XR_002958042.1:n.828G>C
NM_001321268.2:c.165G>C	NP_001308197.1:p.Gln55His
NM_001321269.2:c.774G>C	NP_001308198.1:p.Gln258His
NM_001330397.2:c.774G>C	NP_001317326.1:p.Gln258His
NM_017777.4:c.774G>C MANE Select	NP_060247.2:p.Gln258His