Canonical Allele Identifier: CA8669067

Gene: MKS1

Linked Data

• dbSNP Id: rs751294519
• ExAC: 17:56283528 G / C
• gnomAD v2: 17-56283528-G-C
• gnomAD v4: 17-58206167-G-C
• MyVariant Identifiers: chr17:g.56283528G>C (hg19) ; chr17:g.58206167G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58206167G>C , CM000679.2:g.58206167G>C	GRCh38
NC_000017.10:g.56283528G>C , CM000679.1:g.56283528G>C	GRCh37
NC_000017.9:g.53638527G>C	NCBI36
NG_013020.1:g.18440G>C
NG_013032.1:g.18439C>G , LRG_687:g.18439C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000313863.11:c.*4C>G	ENSP00000316631.6:n.*4C>G
ENST00000393119.7:c.1592C>G MANE Select	ENSP00000376827.2:p.Ala531Gly
ENST00000537529.7:c.1163C>G	ENSP00000442096.3:p.Ala388Gly
ENST00000675753.2:c.*1211C>G	ENSP00000502156.1:n.*1211C>G
ENST00000676787.1:c.1463C>G	ENSP00000503999.1:p.Ala488Gly
ENST00000677111.1:c.*1066C>G	ENSP00000504282.1:n.*1066C>G
ENST00000677160.1:n.2866C>G
ENST00000677416.1:n.2913C>G
ENST00000677486.1:c.*936C>G	ENSP00000503852.1:n.*936C>G
ENST00000677709.1:n.2292C>G
ENST00000678011.1:n.2492C>G
ENST00000678432.1:c.*1366C>G	ENSP00000504452.1:n.*1366C>G
ENST00000678463.1:c.1509C>G	ENSP00000502984.1:p.Gly503=
ENST00000678568.1:c.*916C>G	ENSP00000504754.1:n.*916C>G
ENST00000678641.1:c.*936C>G	ENSP00000503159.1:n.*936C>G
ENST00000678763.1:n.1907C>G
ENST00000313863.10:c.*4C>G	ENSP00000316631.6:n.*4C>G
ENST00000393119.6:c.1592C>G	ENSP00000376827.2:p.Ala531Gly
ENST00000393120.6:c.*999C>G	ENSP00000376828.2:n.*999C>G
ENST00000537529.6:c.1562C>G	ENSP00000442096.2:p.Ala521Gly
ENST00000583577.1:n.418C>G
NM_001165927.1:c.1562C>G , LRG_687t2:c.1562C>G	NP_001159399.1:p.Ala521Gly
NM_017777.3:c.1592C>G , LRG_687t1:c.1592C>G	NP_060247.2:p.Ala531Gly
XM_005257483.3:c.1509C>G	XP_005257540.1:p.Gly503=
XM_005257485.3:c.1080C>G	XP_005257542.1:p.Gly360=
XM_005257486.3:c.983C>G	XP_005257543.1:p.Ala328Gly
XM_006721965.2:c.900C>G	XP_006722028.1:p.Gly300=
XM_011524957.1:c.1518C>G	XP_011523259.1:p.Gly506=
XM_011524958.1:c.1601C>G	XP_011523260.1:p.Ala534Gly
XM_011524959.1:c.*4C>G	XP_011523261.1:n.*4C>G
NM_001321268.1:c.983C>G	NP_001308197.1:p.Ala328Gly
NM_001321269.1:c.1509C>G	NP_001308198.1:p.Gly503=
NM_001330397.1:c.*4C>G	NP_001317326.1:n.*4C>G
XM_005257485.4:c.1080C>G	XP_005257542.1:p.Gly360=
XM_006721965.3:c.900C>G	XP_006722028.1:p.Gly300=
XM_011524957.2:c.1518C>G	XP_011523259.1:p.Gly506=
XM_011524958.2:c.1601C>G	XP_011523260.1:p.Ala534Gly
XM_011524959.2:c.*4C>G	XP_011523261.1:n.*4C>G
XM_017024805.1:c.1163C>G	XP_016880294.1:p.Ala388Gly
XR_002958042.1:n.1520C>G
NM_001321268.2:c.983C>G	NP_001308197.1:p.Ala328Gly
NM_001321269.2:c.1509C>G	NP_001308198.1:p.Gly503=
NM_001330397.2:c.*4C>G	NP_001317326.1:n.*4C>G
NM_017777.4:c.1592C>G MANE Select	NP_060247.2:p.Ala531Gly