Canonical Allele Identifier: CA365840980

Gene: AHI1

Linked Data

• MyVariant Identifiers: chr6:g.135611661G>T (hg19) ; chr6:g.135290523G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135290523G>T , CM000668.2:g.135290523G>T	GRCh38
NC_000006.11:g.135611661G>T , CM000668.1:g.135611661G>T	GRCh37
NC_000006.10:g.135653354G>T	NCBI36
NG_008643.1:g.212243C>A
NG_008643.2:g.212243C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265602.11:c.3488C>A MANE Select	ENSP00000265602.6:p.Ser1163Tyr
ENST00000498558.6:n.529C>A
ENST00000527681.2:c.1157C>A
ENST00000679434.1:c.5104C>A	ENSP00000505592.1:n.5104C>A
ENST00000679450.1:c.3227C>A	ENSP00000506494.1:p.Ser1076Tyr
ENST00000679490.1:n.2863C>A
ENST00000679502.1:n.2361-4876C>A
ENST00000679589.1:c.*3516C>A	ENSP00000506644.1:n.*3516C>A
ENST00000679668.1:c.5020C>A	ENSP00000505364.1:n.5020C>A
ENST00000679672.1:c.*1463C>A	ENSP00000505697.1:n.*1463C>A
ENST00000679711.1:c.1782C>A
ENST00000679742.1:c.4896-4876C>A	ENSP00000504890.1:n.4896-4876C>A
ENST00000679890.1:n.1979C>A
ENST00000679925.1:c.3486-4876C>A	ENSP00000505502.1:n.3486-4876C>A
ENST00000679943.1:c.3549C>A	ENSP00000505663.1:n.3549C>A
ENST00000680071.1:n.4261C>A
ENST00000680119.1:c.3713C>A	ENSP00000506403.1:n.3713C>A
ENST00000680328.1:n.597C>A
ENST00000680337.1:c.944-4876C>A
ENST00000680561.1:n.6229-4876C>A
ENST00000680826.1:c.3673C>A	ENSP00000505224.1:n.3673C>A
ENST00000680840.1:c.3716C>A	ENSP00000505809.1:n.3716C>A
ENST00000680965.1:c.*942C>A	ENSP00000505398.1:n.*942C>A
ENST00000681022.1:c.3488C>A	ENSP00000505121.1:p.Ser1163Tyr
ENST00000681057.1:n.2744-4876C>A
ENST00000681196.1:n.4259-4876C>A
ENST00000681301.1:c.3335C>A	ENSP00000505093.1:p.Ser1112Tyr
ENST00000681331.1:n.1217C>A
ENST00000681332.1:n.4005C>A
ENST00000681340.1:c.3488C>A	ENSP00000505666.1:p.Ser1163Tyr
ENST00000681365.1:c.3488C>A	ENSP00000506604.1:p.Ser1163Tyr
ENST00000681488.1:c.3357C>A	ENSP00000505884.1:n.3357C>A
ENST00000681522.1:c.3488C>A	ENSP00000506005.1:p.Ser1163Tyr
ENST00000681556.1:n.3622C>A
ENST00000681718.1:c.*1975C>A	ENSP00000505266.1:n.*1975C>A
ENST00000681754.1:n.4176C>A
ENST00000681828.1:c.5044C>A	ENSP00000505608.1:n.5044C>A
ENST00000681841.1:c.3488C>A	ENSP00000504965.1:p.Ser1163Tyr
ENST00000681860.1:c.3304C>A	ENSP00000506250.1:n.3304C>A
ENST00000265602.10:c.3488C>A	ENSP00000265602.6:p.Ser1163Tyr
ENST00000367799.6:c.1985-4876C>A
ENST00000367800.8:c.3488C>A	ENSP00000356774.4:p.Ser1163Tyr
ENST00000457866.6:c.3488C>A	ENSP00000388650.2:p.Ser1163Tyr
ENST00000475846.6:c.1918C>A
ENST00000487135.1:n.155-4876C>A
ENST00000498558.5:n.337C>A
ENST00000527681.1:c.97C>A
NM_001134830.1:c.3488C>A	NP_001128302.1:p.Ser1163Tyr
NM_001134831.1:c.3488C>A	NP_001128303.1:p.Ser1163Tyr
NM_017651.4:c.3488C>A	NP_060121.3:p.Ser1163Tyr
XM_011535910.1:c.3488C>A	XP_011534212.1:p.Ser1163Tyr
XM_011535911.1:c.3488C>A	XP_011534213.1:p.Ser1163Tyr
XM_011535914.1:c.*9C>A	XP_011534216.1:n.*9C>A
XM_011535915.1:c.3486-4876C>A	XP_011534217.1:n.3486-4876C>A
XR_942488.1:n.5330C>A
XR_942490.1:n.5328-4876C>A
XR_942493.1:n.5191C>A
XR_942494.1:n.5028C>A
NM_001350503.1:c.3488C>A	NP_001337432.1:p.Ser1163Tyr
NM_001350504.1:c.3486-4876C>A	NP_001337433.1:n.3486-4876C>A
XM_011535910.3:c.3488C>A	XP_011534212.1:p.Ser1163Tyr
XM_011535911.3:c.3488C>A	XP_011534213.1:p.Ser1163Tyr
XM_017010980.2:c.*9C>A	XP_016866469.1:n.*9C>A
XM_017010981.2:c.3434C>A	XP_016866470.1:p.Ser1145Tyr
XM_024446479.1:c.3434C>A	XP_024302247.1:p.Ser1145Tyr
XR_001743479.2:n.5427C>A
XR_001743480.2:n.4255C>A
XR_001743481.2:n.4220C>A
XR_001743482.2:n.4123C>A
XR_001743483.2:n.5425-4876C>A
XR_001743484.2:n.5288C>A
XR_001743485.2:n.3984C>A
XR_001743486.2:n.5286-4876C>A
XR_001743487.2:n.5410C>A
XR_001743488.1:n.5652C>A
XR_001743489.2:n.5125C>A
XR_001743490.2:n.4106C>A
XR_002956286.1:n.3759C>A
XR_002956287.1:n.3757-4876C>A
NM_001134831.2:c.3488C>A MANE Select	NP_001128303.1:p.Ser1163Tyr
NM_001134830.2:c.3488C>A	NP_001128302.1:p.Ser1163Tyr
NM_001350503.2:c.3488C>A	NP_001337432.1:p.Ser1163Tyr
NM_001350504.2:c.3486-4876C>A	NP_001337433.1:n.3486-4876C>A
NM_017651.5:c.3488C>A	NP_060121.3:p.Ser1163Tyr