Canonical Allele Identifier: CA365840787

Gene: AHI1

Linked Data

• MyVariant Identifiers: chr6:g.135611623G>C (hg19) ; chr6:g.135290485G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135290485G>C , CM000668.2:g.135290485G>C	GRCh38
NC_000006.11:g.135611623G>C , CM000668.1:g.135611623G>C	GRCh37
NC_000006.10:g.135653316G>C	NCBI36
NG_008643.1:g.212281C>G
NG_008643.2:g.212281C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265602.11:c.3526C>G MANE Select	ENSP00000265602.6:p.His1176Asp
ENST00000498558.6:n.567C>G
ENST00000527681.2:c.1195C>G
ENST00000679434.1:c.5142C>G	ENSP00000505592.1:n.5142C>G
ENST00000679450.1:c.3265C>G	ENSP00000506494.1:p.His1089Asp
ENST00000679490.1:n.2901C>G
ENST00000679502.1:n.2361-4838C>G
ENST00000679589.1:c.*3554C>G	ENSP00000506644.1:n.*3554C>G
ENST00000679668.1:c.5058C>G	ENSP00000505364.1:n.5058C>G
ENST00000679672.1:c.*1501C>G	ENSP00000505697.1:n.*1501C>G
ENST00000679711.1:c.1820C>G
ENST00000679742.1:c.4896-4838C>G	ENSP00000504890.1:n.4896-4838C>G
ENST00000679890.1:n.2017C>G
ENST00000679925.1:c.3486-4838C>G	ENSP00000505502.1:n.3486-4838C>G
ENST00000679943.1:c.3587C>G	ENSP00000505663.1:n.3587C>G
ENST00000680071.1:n.4299C>G
ENST00000680119.1:c.3751C>G	ENSP00000506403.1:n.3751C>G
ENST00000680328.1:n.635C>G
ENST00000680337.1:c.944-4838C>G
ENST00000680561.1:n.6229-4838C>G
ENST00000680826.1:c.3711C>G	ENSP00000505224.1:n.3711C>G
ENST00000680840.1:c.3754C>G	ENSP00000505809.1:n.3754C>G
ENST00000680965.1:c.*980C>G	ENSP00000505398.1:n.*980C>G
ENST00000681022.1:c.3526C>G	ENSP00000505121.1:p.His1176Asp
ENST00000681057.1:n.2744-4838C>G
ENST00000681196.1:n.4259-4838C>G
ENST00000681301.1:c.3373C>G	ENSP00000505093.1:p.His1125Asp
ENST00000681331.1:n.1255C>G
ENST00000681332.1:n.4043C>G
ENST00000681340.1:c.3526C>G	ENSP00000505666.1:p.His1176Asp
ENST00000681365.1:c.3526C>G	ENSP00000506604.1:p.His1176Asp
ENST00000681488.1:c.3395C>G	ENSP00000505884.1:n.3395C>G
ENST00000681522.1:c.3526C>G	ENSP00000506005.1:p.His1176Asp
ENST00000681556.1:n.3660C>G
ENST00000681718.1:c.*2013C>G	ENSP00000505266.1:n.*2013C>G
ENST00000681754.1:n.4214C>G
ENST00000681828.1:c.5082C>G	ENSP00000505608.1:n.5082C>G
ENST00000681841.1:c.3526C>G	ENSP00000504965.1:p.His1176Asp
ENST00000681860.1:c.3342C>G	ENSP00000506250.1:n.3342C>G
ENST00000265602.10:c.3526C>G	ENSP00000265602.6:p.His1176Asp
ENST00000367799.6:c.1985-4838C>G
ENST00000367800.8:c.3526C>G	ENSP00000356774.4:p.His1176Asp
ENST00000457866.6:c.3526C>G	ENSP00000388650.2:p.His1176Asp
ENST00000475846.6:c.1956C>G
ENST00000487135.1:n.155-4838C>G
ENST00000498558.5:n.375C>G
ENST00000527681.1:c.135C>G
NM_001134830.1:c.3526C>G	NP_001128302.1:p.His1176Asp
NM_001134831.1:c.3526C>G	NP_001128303.1:p.His1176Asp
NM_017651.4:c.3526C>G	NP_060121.3:p.His1176Asp
XM_011535910.1:c.3526C>G	XP_011534212.1:p.His1176Asp
XM_011535911.1:c.3526C>G	XP_011534213.1:p.His1176Asp
XM_011535914.1:c.*47C>G	XP_011534216.1:n.*47C>G
XM_011535915.1:c.3486-4838C>G	XP_011534217.1:n.3486-4838C>G
XR_942488.1:n.5368C>G
XR_942490.1:n.5328-4838C>G
XR_942493.1:n.5229C>G
XR_942494.1:n.5066C>G
NM_001350503.1:c.3526C>G	NP_001337432.1:p.His1176Asp
NM_001350504.1:c.3486-4838C>G	NP_001337433.1:n.3486-4838C>G
XM_011535910.3:c.3526C>G	XP_011534212.1:p.His1176Asp
XM_011535911.3:c.3526C>G	XP_011534213.1:p.His1176Asp
XM_017010980.2:c.*47C>G	XP_016866469.1:n.*47C>G
XM_017010981.2:c.3472C>G	XP_016866470.1:p.His1158Asp
XM_024446479.1:c.3472C>G	XP_024302247.1:p.His1158Asp
XR_001743479.2:n.5465C>G
XR_001743480.2:n.4293C>G
XR_001743481.2:n.4258C>G
XR_001743482.2:n.4161C>G
XR_001743483.2:n.5425-4838C>G
XR_001743484.2:n.5326C>G
XR_001743485.2:n.4022C>G
XR_001743486.2:n.5286-4838C>G
XR_001743487.2:n.5448C>G
XR_001743488.1:n.5690C>G
XR_001743489.2:n.5163C>G
XR_001743490.2:n.4144C>G
XR_002956286.1:n.3797C>G
XR_002956287.1:n.3757-4838C>G
NM_001134831.2:c.3526C>G MANE Select	NP_001128303.1:p.His1176Asp
NM_001134830.2:c.3526C>G	NP_001128302.1:p.His1176Asp
NM_001350503.2:c.3526C>G	NP_001337432.1:p.His1176Asp
NM_001350504.2:c.3486-4838C>G	NP_001337433.1:n.3486-4838C>G
NM_017651.5:c.3526C>G	NP_060121.3:p.His1176Asp