Canonical Allele Identifier: CA432528690

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9517310T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475626T>A , CM000665.2:g.9475626T>A	GRCh38
NC_000003.11:g.9517310T>A , CM000665.1:g.9517310T>A	GRCh37
NC_000003.10:g.9492310T>A	NCBI36
NG_034132.1:g.82927T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682236.1:n.2819T>A
ENST00000682536.1:c.3960T>A	ENSP00000507956.1:p.Gly1320=
ENST00000687014.1:n.4853T>A
ENST00000689167.1:n.2244T>A
ENST00000691925.1:n.6661T>A
ENST00000693430.1:n.6106T>A
ENST00000402198.7:c.3864T>A MANE Select	ENSP00000385852.2:p.Gly1288=
ENST00000663774.1:c.*4010T>A	ENSP00000499452.1:n.*4010T>A
ENST00000665872.1:c.*3933T>A	ENSP00000499600.1:n.*3933T>A
ENST00000666307.1:c.*4238T>A	ENSP00000499402.1:n.*4238T>A
ENST00000670063.1:c.*3969T>A	ENSP00000499725.1:n.*3969T>A
ENST00000302463.10:c.3570T>A	ENSP00000302028.6:p.Gly1190=
ENST00000399686.6:c.2722+470T>A
ENST00000402198.5:c.3864T>A	ENSP00000385852.1:p.Gly1288=
ENST00000406341.5:c.3864T>A	ENSP00000383939.1:p.Gly1288=
ENST00000407969.5:c.3921T>A	ENSP00000384114.1:p.Gly1307=
ENST00000413704.5:c.2900T>A
ENST00000459941.1:n.995T>A
ENST00000466242.5:n.3205T>A
ENST00000466826.1:n.251T>A
ENST00000493918.5:n.4028T>A
NM_001080517.2:c.3864T>A	NP_001073986.1:p.Gly1288=
NM_001292043.1:c.3570T>A	NP_001278972.1:p.Gly1190=
XM_005265301.1:c.3921T>A	XP_005265358.1:p.Gly1307=
XM_005265303.1:c.3864T>A	XP_005265360.1:p.Gly1288=
XM_011533920.1:c.4038T>A	XP_011532222.1:p.Gly1346=
XM_011533921.1:c.4038T>A	XP_011532223.1:p.Gly1346=
XM_011533922.1:c.4017T>A	XP_011532224.1:p.Gly1339=
XM_011533923.1:c.4017T>A	XP_011532225.1:p.Gly1339=
XM_011533924.1:c.4017T>A	XP_011532226.1:p.Gly1339=
XM_011533925.1:c.3999T>A	XP_011532227.1:p.Gly1333=
XM_011533926.1:c.3981T>A	XP_011532228.1:p.Gly1327=
XM_011533927.1:c.3981T>A	XP_011532229.1:p.Gly1327=
XM_011533928.1:c.3960T>A	XP_011532230.1:p.Gly1320=
XM_011533929.1:c.3942T>A	XP_011532231.1:p.Gly1314=
XM_011533930.1:c.3903T>A	XP_011532232.1:p.Gly1301=
XM_011533931.1:c.3627T>A	XP_011532233.1:p.Gly1209=
XM_011533932.1:c.3588T>A	XP_011532234.1:p.Gly1196=
XM_011533933.1:c.3588T>A	XP_011532235.1:p.Gly1196=
NM_001349451.1:c.3570T>A	NP_001336380.1:p.Gly1190=
XM_011533921.2:c.4038T>A	XP_011532223.1:p.Gly1346=
XM_017006767.1:c.4038T>A	XP_016862256.1:p.Gly1346=
XM_017006768.2:c.4017T>A	XP_016862257.1:p.Gly1339=
XM_017006770.1:c.3981T>A	XP_016862259.1:p.Gly1327=
XM_017006771.1:c.3978T>A	XP_016862260.1:p.Gly1326=
XM_017006772.1:c.3942T>A	XP_016862261.1:p.Gly1314=
XM_017006773.1:c.3942T>A	XP_016862262.1:p.Gly1314=
XM_017006774.1:c.3921T>A	XP_016862263.1:p.Gly1307=
XM_017006775.1:c.3885T>A	XP_016862264.1:p.Gly1295=
XM_017006776.1:c.3627T>A	XP_016862265.1:p.Gly1209=
XM_017006777.1:c.3627T>A	XP_016862266.1:p.Gly1209=
XM_017006778.1:c.3627T>A	XP_016862267.1:p.Gly1209=
XM_017006779.1:c.3588T>A	XP_016862268.1:p.Gly1196=
XM_017006780.1:c.3588T>A	XP_016862269.1:p.Gly1196=
XM_017006783.1:c.3360T>A	XP_016862272.1:p.Gly1120=
XM_024453620.1:c.3999T>A	XP_024309388.1:p.Gly1333=
XM_024453621.1:c.3675T>A	XP_024309389.1:p.Gly1225=
XR_001740195.2:n.8247T>A
NM_001080517.3:c.3864T>A MANE Select	NP_001073986.1:p.Gly1288=
NM_001292043.2:c.3570T>A	NP_001278972.1:p.Gly1190=
NM_001349451.2:c.3570T>A	NP_001336380.1:p.Gly1190=