Canonical Allele Identifier: CA400324322

Gene: MKS1

Linked Data

• MyVariant Identifiers: chr17:g.56283529C>A (hg19) ; chr17:g.58206168C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58206168C>A , CM000679.2:g.58206168C>A	GRCh38
NC_000017.10:g.56283529C>A , CM000679.1:g.56283529C>A	GRCh37
NC_000017.9:g.53638528C>A	NCBI36
NG_013020.1:g.18441C>A
NG_013032.1:g.18438G>T , LRG_687:g.18438G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313863.11:c.*3G>T	ENSP00000316631.6:n.*3G>T
ENST00000393119.7:c.1591G>T MANE Select	ENSP00000376827.2:p.Ala531Ser
ENST00000537529.7:c.1162G>T	ENSP00000442096.3:p.Ala388Ser
ENST00000675753.2:c.*1210G>T	ENSP00000502156.1:n.*1210G>T
ENST00000676787.1:c.1462G>T	ENSP00000503999.1:p.Ala488Ser
ENST00000677111.1:c.*1065G>T	ENSP00000504282.1:n.*1065G>T
ENST00000677160.1:n.2865G>T
ENST00000677416.1:n.2912G>T
ENST00000677486.1:c.*935G>T	ENSP00000503852.1:n.*935G>T
ENST00000677709.1:n.2291G>T
ENST00000678011.1:n.2491G>T
ENST00000678432.1:c.*1365G>T	ENSP00000504452.1:n.*1365G>T
ENST00000678463.1:c.1508G>T	ENSP00000502984.1:p.Gly503Val
ENST00000678568.1:c.*915G>T	ENSP00000504754.1:n.*915G>T
ENST00000678641.1:c.*935G>T	ENSP00000503159.1:n.*935G>T
ENST00000678763.1:n.1906G>T
ENST00000313863.10:c.*3G>T	ENSP00000316631.6:n.*3G>T
ENST00000393119.6:c.1591G>T	ENSP00000376827.2:p.Ala531Ser
ENST00000393120.6:c.*998G>T	ENSP00000376828.2:n.*998G>T
ENST00000537529.6:c.1561G>T	ENSP00000442096.2:p.Ala521Ser
ENST00000583577.1:n.417G>T
NM_001165927.1:c.1561G>T , LRG_687t2:c.1561G>T	NP_001159399.1:p.Ala521Ser
NM_017777.3:c.1591G>T , LRG_687t1:c.1591G>T	NP_060247.2:p.Ala531Ser
XM_005257483.3:c.1508G>T	XP_005257540.1:p.Gly503Val
XM_005257485.3:c.1079G>T	XP_005257542.1:p.Gly360Val
XM_005257486.3:c.982G>T	XP_005257543.1:p.Ala328Ser
XM_006721965.2:c.899G>T	XP_006722028.1:p.Gly300Val
XM_011524957.1:c.1517G>T	XP_011523259.1:p.Gly506Val
XM_011524958.1:c.1600G>T	XP_011523260.1:p.Ala534Ser
XM_011524959.1:c.*3G>T	XP_011523261.1:n.*3G>T
NM_001321268.1:c.982G>T	NP_001308197.1:p.Ala328Ser
NM_001321269.1:c.1508G>T	NP_001308198.1:p.Gly503Val
NM_001330397.1:c.*3G>T	NP_001317326.1:n.*3G>T
XM_005257485.4:c.1079G>T	XP_005257542.1:p.Gly360Val
XM_006721965.3:c.899G>T	XP_006722028.1:p.Gly300Val
XM_011524957.2:c.1517G>T	XP_011523259.1:p.Gly506Val
XM_011524958.2:c.1600G>T	XP_011523260.1:p.Ala534Ser
XM_011524959.2:c.*3G>T	XP_011523261.1:n.*3G>T
XM_017024805.1:c.1162G>T	XP_016880294.1:p.Ala388Ser
XR_002958042.1:n.1519G>T
NM_001321268.2:c.982G>T	NP_001308197.1:p.Ala328Ser
NM_001321269.2:c.1508G>T	NP_001308198.1:p.Gly503Val
NM_001330397.2:c.*3G>T	NP_001317326.1:n.*3G>T
NM_017777.4:c.1591G>T MANE Select	NP_060247.2:p.Ala531Ser