Canonical Allele Identifier: CA351693054

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9517401G>T (hg19) ; chr3:g.9475717G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475717G>T , CM000665.2:g.9475717G>T	GRCh38
NC_000003.11:g.9517401G>T , CM000665.1:g.9517401G>T	GRCh37
NC_000003.10:g.9492401G>T	NCBI36
NG_034132.1:g.83018G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682236.1:n.2910G>T
ENST00000682536.1:c.4051G>T	ENSP00000507956.1:p.Gly1351Trp
ENST00000687014.1:n.4944G>T
ENST00000689167.1:n.2335G>T
ENST00000693430.1:n.6197G>T
ENST00000402198.7:c.3955G>T MANE Select	ENSP00000385852.2:p.Gly1319Trp
ENST00000663774.1:c.*4101G>T	ENSP00000499452.1:n.*4101G>T
ENST00000665872.1:c.*4024G>T	ENSP00000499600.1:n.*4024G>T
ENST00000666307.1:c.*4329G>T	ENSP00000499402.1:n.*4329G>T
ENST00000670063.1:c.*4060G>T	ENSP00000499725.1:n.*4060G>T
ENST00000302463.10:c.3661G>T	ENSP00000302028.6:p.Gly1221Trp
ENST00000399686.6:c.2722+561G>T
ENST00000402198.5:c.3955G>T	ENSP00000385852.1:p.Gly1319Trp
ENST00000406341.5:c.3955G>T	ENSP00000383939.1:p.Gly1319Trp
ENST00000407969.5:c.4012G>T	ENSP00000384114.1:p.Gly1338Trp
ENST00000413704.5:c.2991G>T
ENST00000466242.5:n.3296G>T
ENST00000493918.5:n.4119G>T
NM_001080517.2:c.3955G>T	NP_001073986.1:p.Gly1319Trp
NM_001292043.1:c.3661G>T	NP_001278972.1:p.Gly1221Trp
XM_005265301.1:c.4012G>T	XP_005265358.1:p.Gly1338Trp
XM_005265303.1:c.3955G>T	XP_005265360.1:p.Gly1319Trp
XM_011533920.1:c.4129G>T	XP_011532222.1:p.Gly1377Trp
XM_011533921.1:c.4129G>T	XP_011532223.1:p.Gly1377Trp
XM_011533922.1:c.4108G>T	XP_011532224.1:p.Gly1370Trp
XM_011533923.1:c.4108G>T	XP_011532225.1:p.Gly1370Trp
XM_011533924.1:c.4108G>T	XP_011532226.1:p.Gly1370Trp
XM_011533925.1:c.4090G>T	XP_011532227.1:p.Gly1364Trp
XM_011533926.1:c.4072G>T	XP_011532228.1:p.Gly1358Trp
XM_011533927.1:c.4072G>T	XP_011532229.1:p.Gly1358Trp
XM_011533928.1:c.4051G>T	XP_011532230.1:p.Gly1351Trp
XM_011533929.1:c.4033G>T	XP_011532231.1:p.Gly1345Trp
XM_011533930.1:c.3994G>T	XP_011532232.1:p.Gly1332Trp
XM_011533931.1:c.3718G>T	XP_011532233.1:p.Gly1240Trp
XM_011533932.1:c.3679G>T	XP_011532234.1:p.Gly1227Trp
XM_011533933.1:c.3679G>T	XP_011532235.1:p.Gly1227Trp
NM_001349451.1:c.3661G>T	NP_001336380.1:p.Gly1221Trp
XM_011533921.2:c.4129G>T	XP_011532223.1:p.Gly1377Trp
XM_017006767.1:c.4129G>T	XP_016862256.1:p.Gly1377Trp
XM_017006768.2:c.4108G>T	XP_016862257.1:p.Gly1370Trp
XM_017006770.1:c.4072G>T	XP_016862259.1:p.Gly1358Trp
XM_017006771.1:c.4069G>T	XP_016862260.1:p.Gly1357Trp
XM_017006772.1:c.4033G>T	XP_016862261.1:p.Gly1345Trp
XM_017006773.1:c.4033G>T	XP_016862262.1:p.Gly1345Trp
XM_017006774.1:c.4012G>T	XP_016862263.1:p.Gly1338Trp
XM_017006775.1:c.3976G>T	XP_016862264.1:p.Gly1326Trp
XM_017006776.1:c.3718G>T	XP_016862265.1:p.Gly1240Trp
XM_017006777.1:c.3718G>T	XP_016862266.1:p.Gly1240Trp
XM_017006778.1:c.3718G>T	XP_016862267.1:p.Gly1240Trp
XM_017006779.1:c.3679G>T	XP_016862268.1:p.Gly1227Trp
XM_017006780.1:c.3679G>T	XP_016862269.1:p.Gly1227Trp
XM_017006783.1:c.3451G>T	XP_016862272.1:p.Gly1151Trp
XM_024453620.1:c.4090G>T	XP_024309388.1:p.Gly1364Trp
XM_024453621.1:c.3766G>T	XP_024309389.1:p.Gly1256Trp
XR_001740195.2:n.8338G>T
NM_001080517.3:c.3955G>T MANE Select	NP_001073986.1:p.Gly1319Trp
NM_001292043.2:c.3661G>T	NP_001278972.1:p.Gly1221Trp
NM_001349451.2:c.3661G>T	NP_001336380.1:p.Gly1221Trp