Canonical Allele Identifier: CA452341396

Gene: AHI1

Linked Data

• MyVariant Identifiers: chr6:g.135611606C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135290468C>A , CM000668.2:g.135290468C>A	GRCh38
NC_000006.11:g.135611606C>A , CM000668.1:g.135611606C>A	GRCh37
NC_000006.10:g.135653299C>A	NCBI36
NG_008643.1:g.212298G>T
NG_008643.2:g.212298G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265602.11:c.3543G>T MANE Select	ENSP00000265602.6:p.Arg1181=
ENST00000498558.6:n.584G>T
ENST00000527681.2:c.1212G>T
ENST00000679434.1:c.5159G>T	ENSP00000505592.1:n.5159G>T
ENST00000679450.1:c.3282G>T	ENSP00000506494.1:p.Arg1094=
ENST00000679490.1:n.2918G>T
ENST00000679502.1:n.2361-4821G>T
ENST00000679589.1:c.*3571G>T	ENSP00000506644.1:n.*3571G>T
ENST00000679668.1:c.5075G>T	ENSP00000505364.1:n.5075G>T
ENST00000679672.1:c.*1518G>T	ENSP00000505697.1:n.*1518G>T
ENST00000679711.1:c.1837G>T
ENST00000679742.1:c.4896-4821G>T	ENSP00000504890.1:n.4896-4821G>T
ENST00000679890.1:n.2034G>T
ENST00000679925.1:c.3486-4821G>T	ENSP00000505502.1:n.3486-4821G>T
ENST00000679943.1:c.3604G>T	ENSP00000505663.1:n.3604G>T
ENST00000680071.1:n.4316G>T
ENST00000680119.1:c.3768G>T	ENSP00000506403.1:n.3768G>T
ENST00000680328.1:n.652G>T
ENST00000680337.1:c.944-4821G>T
ENST00000680561.1:n.6229-4821G>T
ENST00000680826.1:c.3728G>T	ENSP00000505224.1:n.3728G>T
ENST00000680840.1:c.3771G>T	ENSP00000505809.1:n.3771G>T
ENST00000680965.1:c.*997G>T	ENSP00000505398.1:n.*997G>T
ENST00000681022.1:c.3543G>T	ENSP00000505121.1:p.Arg1181=
ENST00000681057.1:n.2744-4821G>T
ENST00000681196.1:n.4259-4821G>T
ENST00000681301.1:c.3390G>T	ENSP00000505093.1:p.Arg1130=
ENST00000681331.1:n.1272G>T
ENST00000681332.1:n.4060G>T
ENST00000681340.1:c.3543G>T	ENSP00000505666.1:p.Arg1181=
ENST00000681365.1:c.3543G>T	ENSP00000506604.1:p.Arg1181=
ENST00000681488.1:c.3412G>T	ENSP00000505884.1:n.3412G>T
ENST00000681522.1:c.3543G>T	ENSP00000506005.1:p.Arg1181=
ENST00000681556.1:n.3677G>T
ENST00000681718.1:c.*2030G>T	ENSP00000505266.1:n.*2030G>T
ENST00000681754.1:n.4231G>T
ENST00000681828.1:c.5099G>T	ENSP00000505608.1:n.5099G>T
ENST00000681841.1:c.3543G>T	ENSP00000504965.1:p.Arg1181=
ENST00000681860.1:c.3359G>T	ENSP00000506250.1:n.3359G>T
ENST00000265602.10:c.3543G>T	ENSP00000265602.6:p.Arg1181=
ENST00000367799.6:c.1985-4821G>T
ENST00000367800.8:c.3543G>T	ENSP00000356774.4:p.Arg1181=
ENST00000457866.6:c.3543G>T	ENSP00000388650.2:p.Arg1181=
ENST00000475846.6:c.1973G>T
ENST00000487135.1:n.155-4821G>T
ENST00000498558.5:n.392G>T
ENST00000527681.1:c.152G>T
NM_001134830.1:c.3543G>T	NP_001128302.1:p.Arg1181=
NM_001134831.1:c.3543G>T	NP_001128303.1:p.Arg1181=
NM_017651.4:c.3543G>T	NP_060121.3:p.Arg1181=
XM_011535910.1:c.3543G>T	XP_011534212.1:p.Arg1181=
XM_011535911.1:c.3543G>T	XP_011534213.1:p.Arg1181=
XM_011535914.1:c.*64G>T	XP_011534216.1:n.*64G>T
XM_011535915.1:c.3486-4821G>T	XP_011534217.1:n.3486-4821G>T
XR_942488.1:n.5385G>T
XR_942490.1:n.5328-4821G>T
XR_942493.1:n.5246G>T
XR_942494.1:n.5083G>T
NM_001350503.1:c.3543G>T	NP_001337432.1:p.Arg1181=
NM_001350504.1:c.3486-4821G>T	NP_001337433.1:n.3486-4821G>T
XM_011535910.3:c.3543G>T	XP_011534212.1:p.Arg1181=
XM_011535911.3:c.3543G>T	XP_011534213.1:p.Arg1181=
XM_017010980.2:c.*64G>T	XP_016866469.1:n.*64G>T
XM_017010981.2:c.3489G>T	XP_016866470.1:p.Arg1163=
XM_024446479.1:c.3489G>T	XP_024302247.1:p.Arg1163=
XR_001743479.2:n.5482G>T
XR_001743480.2:n.4310G>T
XR_001743481.2:n.4275G>T
XR_001743482.2:n.4178G>T
XR_001743483.2:n.5425-4821G>T
XR_001743484.2:n.5343G>T
XR_001743485.2:n.4039G>T
XR_001743486.2:n.5286-4821G>T
XR_001743487.2:n.5465G>T
XR_001743488.1:n.5707G>T
XR_001743489.2:n.5180G>T
XR_001743490.2:n.4161G>T
XR_002956286.1:n.3814G>T
XR_002956287.1:n.3757-4821G>T
NM_001134831.2:c.3543G>T MANE Select	NP_001128303.1:p.Arg1181=
NM_001134830.2:c.3543G>T	NP_001128302.1:p.Arg1181=
NM_001350503.2:c.3543G>T	NP_001337432.1:p.Arg1181=
NM_001350504.2:c.3486-4821G>T	NP_001337433.1:n.3486-4821G>T
NM_017651.5:c.3543G>T	NP_060121.3:p.Arg1181=