Canonical Allele Identifier: CA351690613

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9517171T>G (hg19) ; chr3:g.9475487T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475487T>G , CM000665.2:g.9475487T>G	GRCh38
NC_000003.11:g.9517171T>G , CM000665.1:g.9517171T>G	GRCh37
NC_000003.10:g.9492171T>G	NCBI36
NG_034132.1:g.82788T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2680T>G
ENST00000682536.1:c.3821T>G	ENSP00000507956.1:p.Leu1274Arg
ENST00000687014.1:n.4714T>G
ENST00000689167.1:n.2105T>G
ENST00000691925.1:n.6522T>G
ENST00000693430.1:n.5967T>G
ENST00000402198.7:c.3725T>G MANE Select	ENSP00000385852.2:p.Leu1242Arg
ENST00000663774.1:c.*3871T>G	ENSP00000499452.1:n.*3871T>G
ENST00000665872.1:c.*3794T>G	ENSP00000499600.1:n.*3794T>G
ENST00000666307.1:c.*4099T>G	ENSP00000499402.1:n.*4099T>G
ENST00000670063.1:c.*3830T>G	ENSP00000499725.1:n.*3830T>G
ENST00000302463.10:c.3431T>G	ENSP00000302028.6:p.Leu1144Arg
ENST00000399686.6:c.2722+331T>G
ENST00000402198.5:c.3725T>G	ENSP00000385852.1:p.Leu1242Arg
ENST00000406341.5:c.3725T>G	ENSP00000383939.1:p.Leu1242Arg
ENST00000407969.5:c.3782T>G	ENSP00000384114.1:p.Leu1261Arg
ENST00000413704.5:c.2761T>G
ENST00000459941.1:n.856T>G
ENST00000466242.5:n.3066T>G
ENST00000466826.1:n.112T>G
ENST00000493918.5:n.3889T>G
NM_001080517.2:c.3725T>G	NP_001073986.1:p.Leu1242Arg
NM_001292043.1:c.3431T>G	NP_001278972.1:p.Leu1144Arg
XM_005265301.1:c.3782T>G	XP_005265358.1:p.Leu1261Arg
XM_005265303.1:c.3725T>G	XP_005265360.1:p.Leu1242Arg
XM_011533920.1:c.3899T>G	XP_011532222.1:p.Leu1300Arg
XM_011533921.1:c.3899T>G	XP_011532223.1:p.Leu1300Arg
XM_011533922.1:c.3878T>G	XP_011532224.1:p.Leu1293Arg
XM_011533923.1:c.3878T>G	XP_011532225.1:p.Leu1293Arg
XM_011533924.1:c.3878T>G	XP_011532226.1:p.Leu1293Arg
XM_011533925.1:c.3860T>G	XP_011532227.1:p.Leu1287Arg
XM_011533926.1:c.3842T>G	XP_011532228.1:p.Leu1281Arg
XM_011533927.1:c.3842T>G	XP_011532229.1:p.Leu1281Arg
XM_011533928.1:c.3821T>G	XP_011532230.1:p.Leu1274Arg
XM_011533929.1:c.3803T>G	XP_011532231.1:p.Leu1268Arg
XM_011533930.1:c.3764T>G	XP_011532232.1:p.Leu1255Arg
XM_011533931.1:c.3488T>G	XP_011532233.1:p.Leu1163Arg
XM_011533932.1:c.3449T>G	XP_011532234.1:p.Leu1150Arg
XM_011533933.1:c.3449T>G	XP_011532235.1:p.Leu1150Arg
NM_001349451.1:c.3431T>G	NP_001336380.1:p.Leu1144Arg
XM_011533921.2:c.3899T>G	XP_011532223.1:p.Leu1300Arg
XM_017006767.1:c.3899T>G	XP_016862256.1:p.Leu1300Arg
XM_017006768.2:c.3878T>G	XP_016862257.1:p.Leu1293Arg
XM_017006770.1:c.3842T>G	XP_016862259.1:p.Leu1281Arg
XM_017006771.1:c.3839T>G	XP_016862260.1:p.Leu1280Arg
XM_017006772.1:c.3803T>G	XP_016862261.1:p.Leu1268Arg
XM_017006773.1:c.3803T>G	XP_016862262.1:p.Leu1268Arg
XM_017006774.1:c.3782T>G	XP_016862263.1:p.Leu1261Arg
XM_017006775.1:c.3746T>G	XP_016862264.1:p.Leu1249Arg
XM_017006776.1:c.3488T>G	XP_016862265.1:p.Leu1163Arg
XM_017006777.1:c.3488T>G	XP_016862266.1:p.Leu1163Arg
XM_017006778.1:c.3488T>G	XP_016862267.1:p.Leu1163Arg
XM_017006779.1:c.3449T>G	XP_016862268.1:p.Leu1150Arg
XM_017006780.1:c.3449T>G	XP_016862269.1:p.Leu1150Arg
XM_017006783.1:c.3221T>G	XP_016862272.1:p.Leu1074Arg
XM_024453620.1:c.3860T>G	XP_024309388.1:p.Leu1287Arg
XM_024453621.1:c.3536T>G	XP_024309389.1:p.Leu1179Arg
XR_001740195.2:n.8108T>G
NM_001080517.3:c.3725T>G MANE Select	NP_001073986.1:p.Leu1242Arg
NM_001292043.2:c.3431T>G	NP_001278972.1:p.Leu1144Arg
NM_001349451.2:c.3431T>G	NP_001336380.1:p.Leu1144Arg