Canonical Allele Identifier: CA501036549

Gene: MKS1

Linked Data

• MyVariant Identifiers: chr17:g.56293488A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58216127A>G , CM000679.2:g.58216127A>G	GRCh38
NC_000017.10:g.56293488A>G , CM000679.1:g.56293488A>G	GRCh37
NC_000017.9:g.53648487A>G	NCBI36
NG_013032.1:g.8479T>C , LRG_687:g.8479T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313863.11:c.378T>C	ENSP00000316631.6:p.Phe126=
ENST00000393119.7:c.378T>C MANE Select	ENSP00000376827.2:p.Phe126=
ENST00000537529.7:c.-52T>C	ENSP00000442096.3:n.-52T>C
ENST00000580127.6:c.378T>C	ENSP00000462423.2:p.Phe126=
ENST00000581180.2:c.378T>C	ENSP00000502288.1:p.Phe126=
ENST00000581761.6:c.378T>C	ENSP00000462129.2:p.Phe126=
ENST00000585134.2:c.378T>C	ENSP00000463826.2:p.Phe126=
ENST00000675753.2:c.378T>C	ENSP00000502156.1:p.Phe126=
ENST00000676787.1:c.378T>C	ENSP00000503999.1:p.Phe126=
ENST00000676975.1:c.39T>C	ENSP00000503970.1:p.Phe13=
ENST00000677076.1:n.403T>C
ENST00000677111.1:c.378T>C	ENSP00000504282.1:p.Phe126=
ENST00000677160.1:n.403T>C
ENST00000677416.1:n.403T>C
ENST00000677475.1:n.406T>C
ENST00000677486.1:c.261+539T>C	ENSP00000503852.1:n.261+539T>C
ENST00000677546.1:c.378T>C	ENSP00000504043.1:p.Phe126=
ENST00000677709.1:n.403T>C
ENST00000677791.1:n.406T>C
ENST00000678011.1:n.403T>C
ENST00000678211.1:n.825T>C
ENST00000678432.1:c.378T>C	ENSP00000504452.1:p.Phe126=
ENST00000678463.1:c.378T>C	ENSP00000502984.1:p.Phe126=
ENST00000678481.1:n.406T>C
ENST00000678568.1:c.191-1289T>C	ENSP00000504754.1:n.191-1289T>C
ENST00000678641.1:c.378T>C	ENSP00000503159.1:p.Phe126=
ENST00000678928.1:n.403T>C
ENST00000679081.1:n.403T>C
ENST00000313863.10:c.378T>C	ENSP00000316631.6:p.Phe126=
ENST00000393119.6:c.378T>C	ENSP00000376827.2:p.Phe126=
ENST00000393120.6:c.378T>C	ENSP00000376828.2:p.Phe126=
ENST00000537529.6:c.348T>C	ENSP00000442096.2:p.Phe116=
ENST00000578789.1:c.*121T>C	ENSP00000462411.1:n.*121T>C
ENST00000580127.5:c.378T>C	ENSP00000462423.1:p.Phe126=
ENST00000581180.1:n.378T>C
ENST00000581761.5:c.191-1289T>C	ENSP00000462129.1:n.191-1289T>C
NM_001165927.1:c.348T>C , LRG_687t2:c.348T>C	NP_001159399.1:p.Phe116=
NM_017777.3:c.378T>C , LRG_687t1:c.378T>C	NP_060247.2:p.Phe126=
XM_005257483.3:c.378T>C	XP_005257540.1:p.Phe126=
XM_005257485.3:c.-112T>C	XP_005257542.1:n.-112T>C
XM_005257486.3:c.-134T>C	XP_005257543.1:n.-134T>C
XM_006721965.2:c.-134T>C	XP_006722028.1:n.-134T>C
XM_011524957.1:c.387T>C	XP_011523259.1:p.Phe129=
XM_011524958.1:c.387T>C	XP_011523260.1:p.Phe129=
XM_011524959.1:c.387T>C	XP_011523261.1:p.Phe129=
XM_011524960.1:c.387T>C	XP_011523262.1:p.Phe129=
XR_934494.1:n.435T>C
NM_001321268.1:c.-134T>C	NP_001308197.1:n.-134T>C
NM_001321269.1:c.378T>C	NP_001308198.1:p.Phe126=
NM_001330397.1:c.378T>C	NP_001317326.1:p.Phe126=
XM_005257485.4:c.-112T>C	XP_005257542.1:n.-112T>C
XM_006721965.3:c.-134T>C	XP_006722028.1:n.-134T>C
XM_011524957.2:c.387T>C	XP_011523259.1:p.Phe129=
XM_011524958.2:c.387T>C	XP_011523260.1:p.Phe129=
XM_011524959.2:c.387T>C	XP_011523261.1:p.Phe129=
XM_011524960.2:c.387T>C	XP_011523262.1:p.Phe129=
XM_017024804.2:c.378T>C	XP_016880293.1:p.Phe126=
XM_017024805.1:c.-112T>C	XP_016880294.1:n.-112T>C
XR_002958042.1:n.432T>C
NM_001321268.2:c.-134T>C	NP_001308197.1:n.-134T>C
NM_001321269.2:c.378T>C	NP_001308198.1:p.Phe126=
NM_001330397.2:c.378T>C	NP_001317326.1:p.Phe126=
NM_017777.4:c.378T>C MANE Select	NP_060247.2:p.Phe126=