Canonical Allele Identifier: CA365840887

Gene: AHI1

Linked Data

• MyVariant Identifiers: chr6:g.135611642C>A (hg19) ; chr6:g.135290504C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135290504C>A , CM000668.2:g.135290504C>A	GRCh38
NC_000006.11:g.135611642C>A , CM000668.1:g.135611642C>A	GRCh37
NC_000006.10:g.135653335C>A	NCBI36
NG_008643.1:g.212262G>T
NG_008643.2:g.212262G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265602.11:c.3507G>T MANE Select	ENSP00000265602.6:p.Gln1169His
ENST00000498558.6:n.548G>T
ENST00000527681.2:c.1176G>T
ENST00000679434.1:c.5123G>T	ENSP00000505592.1:n.5123G>T
ENST00000679450.1:c.3246G>T	ENSP00000506494.1:p.Gln1082His
ENST00000679490.1:n.2882G>T
ENST00000679502.1:n.2361-4857G>T
ENST00000679589.1:c.*3535G>T	ENSP00000506644.1:n.*3535G>T
ENST00000679668.1:c.5039G>T	ENSP00000505364.1:n.5039G>T
ENST00000679672.1:c.*1482G>T	ENSP00000505697.1:n.*1482G>T
ENST00000679711.1:c.1801G>T
ENST00000679742.1:c.4896-4857G>T	ENSP00000504890.1:n.4896-4857G>T
ENST00000679890.1:n.1998G>T
ENST00000679925.1:c.3486-4857G>T	ENSP00000505502.1:n.3486-4857G>T
ENST00000679943.1:c.3568G>T	ENSP00000505663.1:n.3568G>T
ENST00000680071.1:n.4280G>T
ENST00000680119.1:c.3732G>T	ENSP00000506403.1:n.3732G>T
ENST00000680328.1:n.616G>T
ENST00000680337.1:c.944-4857G>T
ENST00000680561.1:n.6229-4857G>T
ENST00000680826.1:c.3692G>T	ENSP00000505224.1:n.3692G>T
ENST00000680840.1:c.3735G>T	ENSP00000505809.1:n.3735G>T
ENST00000680965.1:c.*961G>T	ENSP00000505398.1:n.*961G>T
ENST00000681022.1:c.3507G>T	ENSP00000505121.1:p.Gln1169His
ENST00000681057.1:n.2744-4857G>T
ENST00000681196.1:n.4259-4857G>T
ENST00000681301.1:c.3354G>T	ENSP00000505093.1:p.Gln1118His
ENST00000681331.1:n.1236G>T
ENST00000681332.1:n.4024G>T
ENST00000681340.1:c.3507G>T	ENSP00000505666.1:p.Gln1169His
ENST00000681365.1:c.3507G>T	ENSP00000506604.1:p.Gln1169His
ENST00000681488.1:c.3376G>T	ENSP00000505884.1:n.3376G>T
ENST00000681522.1:c.3507G>T	ENSP00000506005.1:p.Gln1169His
ENST00000681556.1:n.3641G>T
ENST00000681718.1:c.*1994G>T	ENSP00000505266.1:n.*1994G>T
ENST00000681754.1:n.4195G>T
ENST00000681828.1:c.5063G>T	ENSP00000505608.1:n.5063G>T
ENST00000681841.1:c.3507G>T	ENSP00000504965.1:p.Gln1169His
ENST00000681860.1:c.3323G>T	ENSP00000506250.1:n.3323G>T
ENST00000265602.10:c.3507G>T	ENSP00000265602.6:p.Gln1169His
ENST00000367799.6:c.1985-4857G>T
ENST00000367800.8:c.3507G>T	ENSP00000356774.4:p.Gln1169His
ENST00000457866.6:c.3507G>T	ENSP00000388650.2:p.Gln1169His
ENST00000475846.6:c.1937G>T
ENST00000487135.1:n.155-4857G>T
ENST00000498558.5:n.356G>T
ENST00000527681.1:c.116G>T
NM_001134830.1:c.3507G>T	NP_001128302.1:p.Gln1169His
NM_001134831.1:c.3507G>T	NP_001128303.1:p.Gln1169His
NM_017651.4:c.3507G>T	NP_060121.3:p.Gln1169His
XM_011535910.1:c.3507G>T	XP_011534212.1:p.Gln1169His
XM_011535911.1:c.3507G>T	XP_011534213.1:p.Gln1169His
XM_011535914.1:c.*28G>T	XP_011534216.1:n.*28G>T
XM_011535915.1:c.3486-4857G>T	XP_011534217.1:n.3486-4857G>T
XR_942488.1:n.5349G>T
XR_942490.1:n.5328-4857G>T
XR_942493.1:n.5210G>T
XR_942494.1:n.5047G>T
NM_001350503.1:c.3507G>T	NP_001337432.1:p.Gln1169His
NM_001350504.1:c.3486-4857G>T	NP_001337433.1:n.3486-4857G>T
XM_011535910.3:c.3507G>T	XP_011534212.1:p.Gln1169His
XM_011535911.3:c.3507G>T	XP_011534213.1:p.Gln1169His
XM_017010980.2:c.*28G>T	XP_016866469.1:n.*28G>T
XM_017010981.2:c.3453G>T	XP_016866470.1:p.Gln1151His
XM_024446479.1:c.3453G>T	XP_024302247.1:p.Gln1151His
XR_001743479.2:n.5446G>T
XR_001743480.2:n.4274G>T
XR_001743481.2:n.4239G>T
XR_001743482.2:n.4142G>T
XR_001743483.2:n.5425-4857G>T
XR_001743484.2:n.5307G>T
XR_001743485.2:n.4003G>T
XR_001743486.2:n.5286-4857G>T
XR_001743487.2:n.5429G>T
XR_001743488.1:n.5671G>T
XR_001743489.2:n.5144G>T
XR_001743490.2:n.4125G>T
XR_002956286.1:n.3778G>T
XR_002956287.1:n.3757-4857G>T
NM_001134831.2:c.3507G>T MANE Select	NP_001128303.1:p.Gln1169His
NM_001134830.2:c.3507G>T	NP_001128302.1:p.Gln1169His
NM_001350503.2:c.3507G>T	NP_001337432.1:p.Gln1169His
NM_001350504.2:c.3486-4857G>T	NP_001337433.1:n.3486-4857G>T
NM_017651.5:c.3507G>T	NP_060121.3:p.Gln1169His