Canonical Allele Identifier: CA8669392

Gene: MKS1

Linked Data

• dbSNP Id: rs746105434
• ExAC: 17:56290352 C / T
• gnomAD v2: 17-56290352-C-T
• gnomAD v3: 17-58212991-C-T
• gnomAD v4: 17-58212991-C-T
• MyVariant Identifiers: chr17:g.56290352C>T (hg19) ; chr17:g.58212991C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58212991C>T , CM000679.2:g.58212991C>T	GRCh38
NC_000017.10:g.56290352C>T , CM000679.1:g.56290352C>T	GRCh37
NC_000017.9:g.53645351C>T	NCBI36
NG_013032.1:g.11615G>A , LRG_687:g.11615G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313863.11:c.849G>A	ENSP00000316631.6:p.Val283=
ENST00000393119.7:c.849G>A MANE Select	ENSP00000376827.2:p.Val283=
ENST00000537529.7:c.420G>A	ENSP00000442096.3:p.Val140=
ENST00000580127.6:c.849G>A	ENSP00000462423.2:p.Val283=
ENST00000581761.6:c.849G>A	ENSP00000462129.2:p.Val283=
ENST00000585134.2:c.849G>A	ENSP00000463826.2:p.Val283=
ENST00000675753.2:c.*468G>A	ENSP00000502156.1:n.*468G>A
ENST00000676787.1:c.720G>A	ENSP00000503999.1:p.Val240=
ENST00000676975.1:c.714G>A	ENSP00000503970.1:n.714G>A
ENST00000677076.1:n.2123G>A
ENST00000677111.1:c.849G>A	ENSP00000504282.1:p.Val283=
ENST00000677160.1:n.2123G>A
ENST00000677416.1:n.874G>A
ENST00000677475.1:n.2800G>A
ENST00000677486.1:c.*193G>A	ENSP00000503852.1:n.*193G>A
ENST00000677546.1:c.*193G>A	ENSP00000504043.1:n.*193G>A
ENST00000677709.1:n.874G>A
ENST00000678011.1:n.874G>A
ENST00000678211.1:n.2898G>A
ENST00000678432.1:c.*468G>A	ENSP00000504452.1:n.*468G>A
ENST00000678463.1:c.849G>A	ENSP00000502984.1:p.Val283=
ENST00000678481.1:n.650G>A
ENST00000678568.1:c.*256G>A	ENSP00000504754.1:n.*256G>A
ENST00000678641.1:c.*193G>A	ENSP00000503159.1:n.*193G>A
ENST00000678928.1:n.2476G>A
ENST00000679081.1:n.2865G>A
ENST00000313863.10:c.849G>A	ENSP00000316631.6:p.Val283=
ENST00000393119.6:c.849G>A	ENSP00000376827.2:p.Val283=
ENST00000393120.6:c.*256G>A	ENSP00000376828.2:n.*256G>A
ENST00000537529.6:c.819G>A	ENSP00000442096.2:p.Val273=
ENST00000577824.5:c.326G>A
ENST00000581761.5:c.*256G>A	ENSP00000462129.1:n.*256G>A
ENST00000585134.1:c.72G>A	ENSP00000463826.1:p.Val24=
NM_001165927.1:c.819G>A , LRG_687t2:c.819G>A	NP_001159399.1:p.Val273=
NM_017777.3:c.849G>A , LRG_687t1:c.849G>A	NP_060247.2:p.Val283=
XM_005257483.3:c.849G>A	XP_005257540.1:p.Val283=
XM_005257485.3:c.420G>A	XP_005257542.1:p.Val140=
XM_005257486.3:c.240G>A	XP_005257543.1:p.Val80=
XM_006721965.2:c.240G>A	XP_006722028.1:p.Val80=
XM_011524957.1:c.858G>A	XP_011523259.1:p.Val286=
XM_011524958.1:c.858G>A	XP_011523260.1:p.Val286=
XM_011524959.1:c.858G>A	XP_011523261.1:p.Val286=
XM_011524960.1:c.858G>A	XP_011523262.1:p.Val286=
XR_934494.1:n.906G>A
NM_001321268.1:c.240G>A	NP_001308197.1:p.Val80=
NM_001321269.1:c.849G>A	NP_001308198.1:p.Val283=
NM_001330397.1:c.849G>A	NP_001317326.1:p.Val283=
XM_005257485.4:c.420G>A	XP_005257542.1:p.Val140=
XM_006721965.3:c.240G>A	XP_006722028.1:p.Val80=
XM_011524957.2:c.858G>A	XP_011523259.1:p.Val286=
XM_011524958.2:c.858G>A	XP_011523260.1:p.Val286=
XM_011524959.2:c.858G>A	XP_011523261.1:p.Val286=
XM_011524960.2:c.858G>A	XP_011523262.1:p.Val286=
XM_017024804.2:c.849G>A	XP_016880293.1:p.Val283=
XM_017024805.1:c.420G>A	XP_016880294.1:p.Val140=
XR_002958042.1:n.903G>A
NM_001321268.2:c.240G>A	NP_001308197.1:p.Val80=
NM_001321269.2:c.849G>A	NP_001308198.1:p.Val283=
NM_001330397.2:c.849G>A	NP_001317326.1:p.Val283=
NM_017777.4:c.849G>A MANE Select	NP_060247.2:p.Val283=