Canonical Allele Identifier: CA365840772

Gene: AHI1

Linked Data

• gnomAD v4: 6-135290483-G-C
• MyVariant Identifiers: chr6:g.135611621G>C (hg19) ; chr6:g.135290483G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135290483G>C , CM000668.2:g.135290483G>C	GRCh38
NC_000006.11:g.135611621G>C , CM000668.1:g.135611621G>C	GRCh37
NC_000006.10:g.135653314G>C	NCBI36
NG_008643.1:g.212283C>G
NG_008643.2:g.212283C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265602.11:c.3528C>G MANE Select	ENSP00000265602.6:p.His1176Gln
ENST00000498558.6:n.569C>G
ENST00000527681.2:c.1197C>G
ENST00000679434.1:c.5144C>G	ENSP00000505592.1:n.5144C>G
ENST00000679450.1:c.3267C>G	ENSP00000506494.1:p.His1089Gln
ENST00000679490.1:n.2903C>G
ENST00000679502.1:n.2361-4836C>G
ENST00000679589.1:c.*3556C>G	ENSP00000506644.1:n.*3556C>G
ENST00000679668.1:c.5060C>G	ENSP00000505364.1:n.5060C>G
ENST00000679672.1:c.*1503C>G	ENSP00000505697.1:n.*1503C>G
ENST00000679711.1:c.1822C>G
ENST00000679742.1:c.4896-4836C>G	ENSP00000504890.1:n.4896-4836C>G
ENST00000679890.1:n.2019C>G
ENST00000679925.1:c.3486-4836C>G	ENSP00000505502.1:n.3486-4836C>G
ENST00000679943.1:c.3589C>G	ENSP00000505663.1:n.3589C>G
ENST00000680071.1:n.4301C>G
ENST00000680119.1:c.3753C>G	ENSP00000506403.1:n.3753C>G
ENST00000680328.1:n.637C>G
ENST00000680337.1:c.944-4836C>G
ENST00000680561.1:n.6229-4836C>G
ENST00000680826.1:c.3713C>G	ENSP00000505224.1:n.3713C>G
ENST00000680840.1:c.3756C>G	ENSP00000505809.1:n.3756C>G
ENST00000680965.1:c.*982C>G	ENSP00000505398.1:n.*982C>G
ENST00000681022.1:c.3528C>G	ENSP00000505121.1:p.His1176Gln
ENST00000681057.1:n.2744-4836C>G
ENST00000681196.1:n.4259-4836C>G
ENST00000681301.1:c.3375C>G	ENSP00000505093.1:p.His1125Gln
ENST00000681331.1:n.1257C>G
ENST00000681332.1:n.4045C>G
ENST00000681340.1:c.3528C>G	ENSP00000505666.1:p.His1176Gln
ENST00000681365.1:c.3528C>G	ENSP00000506604.1:p.His1176Gln
ENST00000681488.1:c.3397C>G	ENSP00000505884.1:n.3397C>G
ENST00000681522.1:c.3528C>G	ENSP00000506005.1:p.His1176Gln
ENST00000681556.1:n.3662C>G
ENST00000681718.1:c.*2015C>G	ENSP00000505266.1:n.*2015C>G
ENST00000681754.1:n.4216C>G
ENST00000681828.1:c.5084C>G	ENSP00000505608.1:n.5084C>G
ENST00000681841.1:c.3528C>G	ENSP00000504965.1:p.His1176Gln
ENST00000681860.1:c.3344C>G	ENSP00000506250.1:n.3344C>G
ENST00000265602.10:c.3528C>G	ENSP00000265602.6:p.His1176Gln
ENST00000367799.6:c.1985-4836C>G
ENST00000367800.8:c.3528C>G	ENSP00000356774.4:p.His1176Gln
ENST00000457866.6:c.3528C>G	ENSP00000388650.2:p.His1176Gln
ENST00000475846.6:c.1958C>G
ENST00000487135.1:n.155-4836C>G
ENST00000498558.5:n.377C>G
ENST00000527681.1:c.137C>G
NM_001134830.1:c.3528C>G	NP_001128302.1:p.His1176Gln
NM_001134831.1:c.3528C>G	NP_001128303.1:p.His1176Gln
NM_017651.4:c.3528C>G	NP_060121.3:p.His1176Gln
XM_011535910.1:c.3528C>G	XP_011534212.1:p.His1176Gln
XM_011535911.1:c.3528C>G	XP_011534213.1:p.His1176Gln
XM_011535914.1:c.*49C>G	XP_011534216.1:n.*49C>G
XM_011535915.1:c.3486-4836C>G	XP_011534217.1:n.3486-4836C>G
XR_942488.1:n.5370C>G
XR_942490.1:n.5328-4836C>G
XR_942493.1:n.5231C>G
XR_942494.1:n.5068C>G
NM_001350503.1:c.3528C>G	NP_001337432.1:p.His1176Gln
NM_001350504.1:c.3486-4836C>G	NP_001337433.1:n.3486-4836C>G
XM_011535910.3:c.3528C>G	XP_011534212.1:p.His1176Gln
XM_011535911.3:c.3528C>G	XP_011534213.1:p.His1176Gln
XM_017010980.2:c.*49C>G	XP_016866469.1:n.*49C>G
XM_017010981.2:c.3474C>G	XP_016866470.1:p.His1158Gln
XM_024446479.1:c.3474C>G	XP_024302247.1:p.His1158Gln
XR_001743479.2:n.5467C>G
XR_001743480.2:n.4295C>G
XR_001743481.2:n.4260C>G
XR_001743482.2:n.4163C>G
XR_001743483.2:n.5425-4836C>G
XR_001743484.2:n.5328C>G
XR_001743485.2:n.4024C>G
XR_001743486.2:n.5286-4836C>G
XR_001743487.2:n.5450C>G
XR_001743488.1:n.5692C>G
XR_001743489.2:n.5165C>G
XR_001743490.2:n.4146C>G
XR_002956286.1:n.3799C>G
XR_002956287.1:n.3757-4836C>G
NM_001134831.2:c.3528C>G MANE Select	NP_001128303.1:p.His1176Gln
NM_001134830.2:c.3528C>G	NP_001128302.1:p.His1176Gln
NM_001350503.2:c.3528C>G	NP_001337432.1:p.His1176Gln
NM_001350504.2:c.3486-4836C>G	NP_001337433.1:n.3486-4836C>G
NM_017651.5:c.3528C>G	NP_060121.3:p.His1176Gln