Canonical Allele Identifier: CA351690869

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9517215C>G (hg19) ; chr3:g.9475531C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475531C>G , CM000665.2:g.9475531C>G	GRCh38
NC_000003.11:g.9517215C>G , CM000665.1:g.9517215C>G	GRCh37
NC_000003.10:g.9492215C>G	NCBI36
NG_034132.1:g.82832C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682236.1:n.2724C>G
ENST00000682536.1:c.3865C>G	ENSP00000507956.1:p.Gln1289Glu
ENST00000687014.1:n.4758C>G
ENST00000689167.1:n.2149C>G
ENST00000691925.1:n.6566C>G
ENST00000693430.1:n.6011C>G
ENST00000402198.7:c.3769C>G MANE Select	ENSP00000385852.2:p.Gln1257Glu
ENST00000663774.1:c.*3915C>G	ENSP00000499452.1:n.*3915C>G
ENST00000665872.1:c.*3838C>G	ENSP00000499600.1:n.*3838C>G
ENST00000666307.1:c.*4143C>G	ENSP00000499402.1:n.*4143C>G
ENST00000670063.1:c.*3874C>G	ENSP00000499725.1:n.*3874C>G
ENST00000302463.10:c.3475C>G	ENSP00000302028.6:p.Gln1159Glu
ENST00000399686.6:c.2722+375C>G
ENST00000402198.5:c.3769C>G	ENSP00000385852.1:p.Gln1257Glu
ENST00000406341.5:c.3769C>G	ENSP00000383939.1:p.Gln1257Glu
ENST00000407969.5:c.3826C>G	ENSP00000384114.1:p.Gln1276Glu
ENST00000413704.5:c.2805C>G
ENST00000459941.1:n.900C>G
ENST00000466242.5:n.3110C>G
ENST00000466826.1:n.156C>G
ENST00000493918.5:n.3933C>G
NM_001080517.2:c.3769C>G	NP_001073986.1:p.Gln1257Glu
NM_001292043.1:c.3475C>G	NP_001278972.1:p.Gln1159Glu
XM_005265301.1:c.3826C>G	XP_005265358.1:p.Gln1276Glu
XM_005265303.1:c.3769C>G	XP_005265360.1:p.Gln1257Glu
XM_011533920.1:c.3943C>G	XP_011532222.1:p.Gln1315Glu
XM_011533921.1:c.3943C>G	XP_011532223.1:p.Gln1315Glu
XM_011533922.1:c.3922C>G	XP_011532224.1:p.Gln1308Glu
XM_011533923.1:c.3922C>G	XP_011532225.1:p.Gln1308Glu
XM_011533924.1:c.3922C>G	XP_011532226.1:p.Gln1308Glu
XM_011533925.1:c.3904C>G	XP_011532227.1:p.Gln1302Glu
XM_011533926.1:c.3886C>G	XP_011532228.1:p.Gln1296Glu
XM_011533927.1:c.3886C>G	XP_011532229.1:p.Gln1296Glu
XM_011533928.1:c.3865C>G	XP_011532230.1:p.Gln1289Glu
XM_011533929.1:c.3847C>G	XP_011532231.1:p.Gln1283Glu
XM_011533930.1:c.3808C>G	XP_011532232.1:p.Gln1270Glu
XM_011533931.1:c.3532C>G	XP_011532233.1:p.Gln1178Glu
XM_011533932.1:c.3493C>G	XP_011532234.1:p.Gln1165Glu
XM_011533933.1:c.3493C>G	XP_011532235.1:p.Gln1165Glu
NM_001349451.1:c.3475C>G	NP_001336380.1:p.Gln1159Glu
XM_011533921.2:c.3943C>G	XP_011532223.1:p.Gln1315Glu
XM_017006767.1:c.3943C>G	XP_016862256.1:p.Gln1315Glu
XM_017006768.2:c.3922C>G	XP_016862257.1:p.Gln1308Glu
XM_017006770.1:c.3886C>G	XP_016862259.1:p.Gln1296Glu
XM_017006771.1:c.3883C>G	XP_016862260.1:p.Gln1295Glu
XM_017006772.1:c.3847C>G	XP_016862261.1:p.Gln1283Glu
XM_017006773.1:c.3847C>G	XP_016862262.1:p.Gln1283Glu
XM_017006774.1:c.3826C>G	XP_016862263.1:p.Gln1276Glu
XM_017006775.1:c.3790C>G	XP_016862264.1:p.Gln1264Glu
XM_017006776.1:c.3532C>G	XP_016862265.1:p.Gln1178Glu
XM_017006777.1:c.3532C>G	XP_016862266.1:p.Gln1178Glu
XM_017006778.1:c.3532C>G	XP_016862267.1:p.Gln1178Glu
XM_017006779.1:c.3493C>G	XP_016862268.1:p.Gln1165Glu
XM_017006780.1:c.3493C>G	XP_016862269.1:p.Gln1165Glu
XM_017006783.1:c.3265C>G	XP_016862272.1:p.Gln1089Glu
XM_024453620.1:c.3904C>G	XP_024309388.1:p.Gln1302Glu
XM_024453621.1:c.3580C>G	XP_024309389.1:p.Gln1194Glu
XR_001740195.2:n.8152C>G
NM_001080517.3:c.3769C>G MANE Select	NP_001073986.1:p.Gln1257Glu
NM_001292043.2:c.3475C>G	NP_001278972.1:p.Gln1159Glu
NM_001349451.2:c.3475C>G	NP_001336380.1:p.Gln1159Glu