Canonical Allele Identifier: CA2573154370
Gene: MKS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1480979
ClinVar RCV Id: RCV001988198

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58206121_58206349del , CM000679.2:g.58206121_58206349del GRCh38
NC_000017.10:g.56283482_56283710del , CM000679.1:g.56283482_56283710del GRCh37
NC_000017.9:g.53638481_53638709del NCBI36
NG_013020.1:g.18394_18622del
NG_013032.1:g.18257_18485del , LRG_687:g.18257_18485del

Transcript Alleles

HGVS Amino-acid change
ENST00000313863.11:c.1305_*50del
ENST00000393119.7:c.1522_1638del
ENST00000537529.7:c.1093_1209del
ENST00000675753.2:c.*1141_*1257del
ENST00000676787.1:c.1393_1509del
ENST00000677111.1:c.*996_*1112del
ENST00000677160.1:n.2796_2912del
ENST00000677416.1:n.2843_2959del
ENST00000677486.1:c.*866_*982del
ENST00000677709.1:n.2222_2338del
ENST00000678011.1:n.2422_2538del
ENST00000678432.1:c.*1296_*1412del
ENST00000678463.1:c.1439_1555del
ENST00000678568.1:c.*846_*962del
ENST00000678641.1:c.*866_*982del
ENST00000678763.1:n.1837_1953del
ENST00000313863.10:c.1305_*50del
ENST00000393119.6:c.1522_1638del
ENST00000393120.6:c.*929_*1045del
ENST00000537529.6:c.1492_1608del
ENST00000583577.1:n.348_464del
NM_001165927.1:c.1492_1608del , LRG_687t2:c.1492_1608del
NM_017777.3:c.1522_1638del , LRG_687t1:c.1522_1638del
XM_005257483.3:c.1439_1555del
XM_005257485.3:c.1010_1126del
XM_005257486.3:c.913_1029del
XM_006721965.2:c.830_946del
XM_011524957.1:c.1448_1564del
XM_011524958.1:c.1531_1647del
XM_011524959.1:c.1314_*50del
NM_001321268.1:c.913_1029del
NM_001321269.1:c.1439_1555del
NM_001330397.1:c.1305_*50del
XM_005257485.4:c.1010_1126del
XM_006721965.3:c.830_946del
XM_011524957.2:c.1448_1564del
XM_011524958.2:c.1531_1647del
XM_011524959.2:c.1314_*50del
XM_017024805.1:c.1093_1209del
XR_002958042.1:n.1450_1566del
NM_001321268.2:c.913_1029del
NM_001321269.2:c.1439_1555del
NM_001330397.2:c.1305_*50del
NM_017777.4:c.1522_1638del