Canonical Allele Identifier: CA365840856

Gene: AHI1

Linked Data

• MyVariant Identifiers: chr6:g.135611636A>C (hg19) ; chr6:g.135290498A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135290498A>C , CM000668.2:g.135290498A>C	GRCh38
NC_000006.11:g.135611636A>C , CM000668.1:g.135611636A>C	GRCh37
NC_000006.10:g.135653329A>C	NCBI36
NG_008643.1:g.212268T>G
NG_008643.2:g.212268T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265602.11:c.3513T>G MANE Select	ENSP00000265602.6:p.His1171Gln
ENST00000498558.6:n.554T>G
ENST00000527681.2:c.1182T>G
ENST00000679434.1:c.5129T>G	ENSP00000505592.1:n.5129T>G
ENST00000679450.1:c.3252T>G	ENSP00000506494.1:p.His1084Gln
ENST00000679490.1:n.2888T>G
ENST00000679502.1:n.2361-4851T>G
ENST00000679589.1:c.*3541T>G	ENSP00000506644.1:n.*3541T>G
ENST00000679668.1:c.5045T>G	ENSP00000505364.1:n.5045T>G
ENST00000679672.1:c.*1488T>G	ENSP00000505697.1:n.*1488T>G
ENST00000679711.1:c.1807T>G
ENST00000679742.1:c.4896-4851T>G	ENSP00000504890.1:n.4896-4851T>G
ENST00000679890.1:n.2004T>G
ENST00000679925.1:c.3486-4851T>G	ENSP00000505502.1:n.3486-4851T>G
ENST00000679943.1:c.3574T>G	ENSP00000505663.1:n.3574T>G
ENST00000680071.1:n.4286T>G
ENST00000680119.1:c.3738T>G	ENSP00000506403.1:n.3738T>G
ENST00000680328.1:n.622T>G
ENST00000680337.1:c.944-4851T>G
ENST00000680561.1:n.6229-4851T>G
ENST00000680826.1:c.3698T>G	ENSP00000505224.1:n.3698T>G
ENST00000680840.1:c.3741T>G	ENSP00000505809.1:n.3741T>G
ENST00000680965.1:c.*967T>G	ENSP00000505398.1:n.*967T>G
ENST00000681022.1:c.3513T>G	ENSP00000505121.1:p.His1171Gln
ENST00000681057.1:n.2744-4851T>G
ENST00000681196.1:n.4259-4851T>G
ENST00000681301.1:c.3360T>G	ENSP00000505093.1:p.His1120Gln
ENST00000681331.1:n.1242T>G
ENST00000681332.1:n.4030T>G
ENST00000681340.1:c.3513T>G	ENSP00000505666.1:p.His1171Gln
ENST00000681365.1:c.3513T>G	ENSP00000506604.1:p.His1171Gln
ENST00000681488.1:c.3382T>G	ENSP00000505884.1:n.3382T>G
ENST00000681522.1:c.3513T>G	ENSP00000506005.1:p.His1171Gln
ENST00000681556.1:n.3647T>G
ENST00000681718.1:c.*2000T>G	ENSP00000505266.1:n.*2000T>G
ENST00000681754.1:n.4201T>G
ENST00000681828.1:c.5069T>G	ENSP00000505608.1:n.5069T>G
ENST00000681841.1:c.3513T>G	ENSP00000504965.1:p.His1171Gln
ENST00000681860.1:c.3329T>G	ENSP00000506250.1:n.3329T>G
ENST00000265602.10:c.3513T>G	ENSP00000265602.6:p.His1171Gln
ENST00000367799.6:c.1985-4851T>G
ENST00000367800.8:c.3513T>G	ENSP00000356774.4:p.His1171Gln
ENST00000457866.6:c.3513T>G	ENSP00000388650.2:p.His1171Gln
ENST00000475846.6:c.1943T>G
ENST00000487135.1:n.155-4851T>G
ENST00000498558.5:n.362T>G
ENST00000527681.1:c.122T>G
NM_001134830.1:c.3513T>G	NP_001128302.1:p.His1171Gln
NM_001134831.1:c.3513T>G	NP_001128303.1:p.His1171Gln
NM_017651.4:c.3513T>G	NP_060121.3:p.His1171Gln
XM_011535910.1:c.3513T>G	XP_011534212.1:p.His1171Gln
XM_011535911.1:c.3513T>G	XP_011534213.1:p.His1171Gln
XM_011535914.1:c.*34T>G	XP_011534216.1:n.*34T>G
XM_011535915.1:c.3486-4851T>G	XP_011534217.1:n.3486-4851T>G
XR_942488.1:n.5355T>G
XR_942490.1:n.5328-4851T>G
XR_942493.1:n.5216T>G
XR_942494.1:n.5053T>G
NM_001350503.1:c.3513T>G	NP_001337432.1:p.His1171Gln
NM_001350504.1:c.3486-4851T>G	NP_001337433.1:n.3486-4851T>G
XM_011535910.3:c.3513T>G	XP_011534212.1:p.His1171Gln
XM_011535911.3:c.3513T>G	XP_011534213.1:p.His1171Gln
XM_017010980.2:c.*34T>G	XP_016866469.1:n.*34T>G
XM_017010981.2:c.3459T>G	XP_016866470.1:p.His1153Gln
XM_024446479.1:c.3459T>G	XP_024302247.1:p.His1153Gln
XR_001743479.2:n.5452T>G
XR_001743480.2:n.4280T>G
XR_001743481.2:n.4245T>G
XR_001743482.2:n.4148T>G
XR_001743483.2:n.5425-4851T>G
XR_001743484.2:n.5313T>G
XR_001743485.2:n.4009T>G
XR_001743486.2:n.5286-4851T>G
XR_001743487.2:n.5435T>G
XR_001743488.1:n.5677T>G
XR_001743489.2:n.5150T>G
XR_001743490.2:n.4131T>G
XR_002956286.1:n.3784T>G
XR_002956287.1:n.3757-4851T>G
NM_001134831.2:c.3513T>G MANE Select	NP_001128303.1:p.His1171Gln
NM_001134830.2:c.3513T>G	NP_001128302.1:p.His1171Gln
NM_001350503.2:c.3513T>G	NP_001337432.1:p.His1171Gln
NM_001350504.2:c.3486-4851T>G	NP_001337433.1:n.3486-4851T>G
NM_017651.5:c.3513T>G	NP_060121.3:p.His1171Gln