Canonical Allele Identifier: CA8669223

Gene: MKS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58207934A>G , CM000679.2:g.58207934A>G	GRCh38
NC_000017.10:g.56285295A>G , CM000679.1:g.56285295A>G	GRCh37
NC_000017.9:g.53640294A>G	NCBI36
NG_013032.1:g.16672T>C , LRG_687:g.16672T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313863.11:c.1233T>C	ENSP00000316631.6:p.Arg411=
ENST00000393119.7:c.1233T>C MANE Select	ENSP00000376827.2:p.Arg411=
ENST00000537529.7:c.804T>C	ENSP00000442096.3:p.Arg268=
ENST00000580127.6:c.1233T>C	ENSP00000462423.2:p.Arg411=
ENST00000585134.2:c.1233T>C	ENSP00000463826.2:p.Arg411=
ENST00000675753.2:c.*852T>C	ENSP00000502156.1:n.*852T>C
ENST00000676787.1:c.1104T>C	ENSP00000503999.1:p.Arg368=
ENST00000677111.1:c.*170T>C	ENSP00000504282.1:n.*170T>C
ENST00000677160.1:n.2507T>C
ENST00000677416.1:n.1258T>C
ENST00000677486.1:c.*577T>C	ENSP00000503852.1:n.*577T>C
ENST00000677709.1:n.1258T>C
ENST00000678011.1:n.1596T>C
ENST00000678432.1:c.*852T>C	ENSP00000504452.1:n.*852T>C
ENST00000678463.1:c.1233T>C	ENSP00000502984.1:p.Arg411=
ENST00000678568.1:c.*640T>C	ENSP00000504754.1:n.*640T>C
ENST00000678641.1:c.*577T>C	ENSP00000503159.1:n.*577T>C
ENST00000678763.1:n.1011T>C
ENST00000313863.10:c.1233T>C	ENSP00000316631.6:p.Arg411=
ENST00000393119.6:c.1233T>C	ENSP00000376827.2:p.Arg411=
ENST00000393120.6:c.*640T>C	ENSP00000376828.2:n.*640T>C
ENST00000537529.6:c.1203T>C	ENSP00000442096.2:p.Arg401=
ENST00000577315.5:c.286T>C
ENST00000577824.5:c.786T>C
ENST00000585134.1:c.456T>C	ENSP00000463826.1:p.Arg152=
NM_001165927.1:c.1203T>C , LRG_687t2:c.1203T>C	NP_001159399.1:p.Arg401=
NM_017777.3:c.1233T>C , LRG_687t1:c.1233T>C	NP_060247.2:p.Arg411=
XM_005257483.3:c.1233T>C	XP_005257540.1:p.Arg411=
XM_005257485.3:c.804T>C	XP_005257542.1:p.Arg268=
XM_005257486.3:c.624T>C	XP_005257543.1:p.Arg208=
XM_006721965.2:c.624T>C	XP_006722028.1:p.Arg208=
XM_011524957.1:c.1242T>C	XP_011523259.1:p.Arg414=
XM_011524958.1:c.1242T>C	XP_011523260.1:p.Arg414=
XM_011524959.1:c.1242T>C	XP_011523261.1:p.Arg414=
XM_011524960.1:c.1242T>C	XP_011523262.1:p.Arg414=
XR_934494.1:n.1247T>C
NM_001321268.1:c.624T>C	NP_001308197.1:p.Arg208=
NM_001321269.1:c.1233T>C	NP_001308198.1:p.Arg411=
NM_001330397.1:c.1233T>C	NP_001317326.1:p.Arg411=
XM_005257485.4:c.804T>C	XP_005257542.1:p.Arg268=
XM_006721965.3:c.624T>C	XP_006722028.1:p.Arg208=
XM_011524957.2:c.1242T>C	XP_011523259.1:p.Arg414=
XM_011524958.2:c.1242T>C	XP_011523260.1:p.Arg414=
XM_011524959.2:c.1242T>C	XP_011523261.1:p.Arg414=
XM_011524960.2:c.1242T>C	XP_011523262.1:p.Arg414=
XM_017024804.2:c.1233T>C	XP_016880293.1:p.Arg411=
XM_017024805.1:c.804T>C	XP_016880294.1:p.Arg268=
XR_002958042.1:n.1244T>C
NM_001321268.2:c.624T>C	NP_001308197.1:p.Arg208=
NM_001321269.2:c.1233T>C	NP_001308198.1:p.Arg411=
NM_001330397.2:c.1233T>C	NP_001317326.1:p.Arg411=
NM_017777.4:c.1233T>C MANE Select	NP_060247.2:p.Arg411=