Canonical Allele Identifier: CA2740093821

Gene: MKS1

Linked Data

• ClinVar Variation Id: 2946493
• ClinVar RCV Id: RCV003808731

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58206397C>A , CM000679.2:g.58206397C>A	GRCh38
NC_000017.10:g.56283758C>A , CM000679.1:g.56283758C>A	GRCh37
NC_000017.9:g.53638757C>A	NCBI36
NG_013020.1:g.18670C>A
NG_013032.1:g.18209G>T , LRG_687:g.18209G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313863.11:c.1274-17G>T	ENSP00000316631.6:n.1274-17G>T
ENST00000393119.7:c.1491-17G>T MANE Select	ENSP00000376827.2:n.1491-17G>T
ENST00000537529.7:c.1062-17G>T	ENSP00000442096.3:n.1062-17G>T
ENST00000675753.2:c.*1110-17G>T	ENSP00000502156.1:n.*1110-17G>T
ENST00000676787.1:c.1362-17G>T	ENSP00000503999.1:n.1362-17G>T
ENST00000677111.1:c.*965-17G>T	ENSP00000504282.1:n.*965-17G>T
ENST00000677160.1:n.2765-17G>T
ENST00000677416.1:n.2795G>T
ENST00000677486.1:c.*835-17G>T	ENSP00000503852.1:n.*835-17G>T
ENST00000677709.1:n.2191-17G>T
ENST00000678011.1:n.2391-17G>T
ENST00000678432.1:c.*1265-17G>T	ENSP00000504452.1:n.*1265-17G>T
ENST00000678463.1:c.1408-17G>T	ENSP00000502984.1:n.1408-17G>T
ENST00000678568.1:c.*815-17G>T	ENSP00000504754.1:n.*815-17G>T
ENST00000678641.1:c.*835-17G>T	ENSP00000503159.1:n.*835-17G>T
ENST00000678763.1:n.1806-17G>T
ENST00000313863.10:c.1274-17G>T	ENSP00000316631.6:n.1274-17G>T
ENST00000393119.6:c.1491-17G>T	ENSP00000376827.2:n.1491-17G>T
ENST00000393120.6:c.*898-17G>T	ENSP00000376828.2:n.*898-17G>T
ENST00000537529.6:c.1461-17G>T	ENSP00000442096.2:n.1461-17G>T
ENST00000583577.1:n.317-17G>T
NM_001165927.1:c.1461-17G>T , LRG_687t2:c.1461-17G>T	NP_001159399.1:n.1461-17G>T
NM_017777.3:c.1491-17G>T , LRG_687t1:c.1491-17G>T	NP_060247.2:n.1491-17G>T
XM_005257483.3:c.1408-17G>T	XP_005257540.1:n.1408-17G>T
XM_005257485.3:c.979-17G>T	XP_005257542.1:n.979-17G>T
XM_005257486.3:c.882-17G>T	XP_005257543.1:n.882-17G>T
XM_006721965.2:c.799-17G>T	XP_006722028.1:n.799-17G>T
XM_011524957.1:c.1417-17G>T	XP_011523259.1:n.1417-17G>T
XM_011524958.1:c.1500-17G>T	XP_011523260.1:n.1500-17G>T
XM_011524959.1:c.1283-17G>T	XP_011523261.1:n.1283-17G>T
NM_001321268.1:c.882-17G>T	NP_001308197.1:n.882-17G>T
NM_001321269.1:c.1408-17G>T	NP_001308198.1:n.1408-17G>T
NM_001330397.1:c.1274-17G>T	NP_001317326.1:n.1274-17G>T
XM_005257485.4:c.979-17G>T	XP_005257542.1:n.979-17G>T
XM_006721965.3:c.799-17G>T	XP_006722028.1:n.799-17G>T
XM_011524957.2:c.1417-17G>T	XP_011523259.1:n.1417-17G>T
XM_011524958.2:c.1500-17G>T	XP_011523260.1:n.1500-17G>T
XM_011524959.2:c.1283-17G>T	XP_011523261.1:n.1283-17G>T
XM_017024805.1:c.1062-17G>T	XP_016880294.1:n.1062-17G>T
XR_002958042.1:n.1419-17G>T
NM_001321268.2:c.882-17G>T	NP_001308197.1:n.882-17G>T
NM_001321269.2:c.1408-17G>T	NP_001308198.1:n.1408-17G>T
NM_001330397.2:c.1274-17G>T	NP_001317326.1:n.1274-17G>T
NM_017777.4:c.1491-17G>T MANE Select	NP_060247.2:n.1491-17G>T