Canonical Allele Identifier: CA1344742707

Gene: SETD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475708G= , CM000665.2:g.9475708G=	GRCh38
NC_000003.11:g.9517392G= , CM000665.1:g.9517392G=	GRCh37
NC_000003.10:g.9492392G=	NCBI36
NG_034132.1:g.83009G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2901G=
ENST00000682536.1:c.4042G=	ENSP00000507956.1:p.Gly1348=
ENST00000687014.1:n.4935G=
ENST00000689167.1:n.2326G=
ENST00000693430.1:n.6188G=
ENST00000402198.7:c.3946G= MANE Select	ENSP00000385852.2:p.Gly1316=
ENST00000663774.1:c.*4092G=	ENSP00000499452.1:n.*4092G=
ENST00000665872.1:c.*4015G=	ENSP00000499600.1:n.*4015G=
ENST00000666307.1:c.*4320G=	ENSP00000499402.1:n.*4320G=
ENST00000670063.1:c.*4051G=	ENSP00000499725.1:n.*4051G=
ENST00000302463.10:c.3652G=	ENSP00000302028.6:p.Gly1218=
ENST00000399686.6:c.2722+552G=
ENST00000402198.5:c.3946G=	ENSP00000385852.1:p.Gly1316=
ENST00000406341.5:c.3946G=	ENSP00000383939.1:p.Gly1316=
ENST00000407969.5:c.4003G=	ENSP00000384114.1:p.Gly1335=
ENST00000413704.5:c.2982G=
ENST00000466242.5:n.3287G=
ENST00000493918.5:n.4110G=
NM_001080517.2:c.3946G=	NP_001073986.1:p.Gly1316=
NM_001292043.1:c.3652G=	NP_001278972.1:p.Gly1218=
XM_005265301.1:c.4003G=	XP_005265358.1:p.Gly1335=
XM_005265303.1:c.3946G=	XP_005265360.1:p.Gly1316=
XM_011533920.1:c.4120G=	XP_011532222.1:p.Gly1374=
XM_011533921.1:c.4120G=	XP_011532223.1:p.Gly1374=
XM_011533922.1:c.4099G=	XP_011532224.1:p.Gly1367=
XM_011533923.1:c.4099G=	XP_011532225.1:p.Gly1367=
XM_011533924.1:c.4099G=	XP_011532226.1:p.Gly1367=
XM_011533925.1:c.4081G=	XP_011532227.1:p.Gly1361=
XM_011533926.1:c.4063G=	XP_011532228.1:p.Gly1355=
XM_011533927.1:c.4063G=	XP_011532229.1:p.Gly1355=
XM_011533928.1:c.4042G=	XP_011532230.1:p.Gly1348=
XM_011533929.1:c.4024G=	XP_011532231.1:p.Gly1342=
XM_011533930.1:c.3985G=	XP_011532232.1:p.Gly1329=
XM_011533931.1:c.3709G=	XP_011532233.1:p.Gly1237=
XM_011533932.1:c.3670G=	XP_011532234.1:p.Gly1224=
XM_011533933.1:c.3670G=	XP_011532235.1:p.Gly1224=
NM_001349451.1:c.3652G=	NP_001336380.1:p.Gly1218=
XM_011533921.2:c.4120G=	XP_011532223.1:p.Gly1374=
XM_017006767.1:c.4120G=	XP_016862256.1:p.Gly1374=
XM_017006768.2:c.4099G=	XP_016862257.1:p.Gly1367=
XM_017006770.1:c.4063G=	XP_016862259.1:p.Gly1355=
XM_017006771.1:c.4060G=	XP_016862260.1:p.Gly1354=
XM_017006772.1:c.4024G=	XP_016862261.1:p.Gly1342=
XM_017006773.1:c.4024G=	XP_016862262.1:p.Gly1342=
XM_017006774.1:c.4003G=	XP_016862263.1:p.Gly1335=
XM_017006775.1:c.3967G=	XP_016862264.1:p.Gly1323=
XM_017006776.1:c.3709G=	XP_016862265.1:p.Gly1237=
XM_017006777.1:c.3709G=	XP_016862266.1:p.Gly1237=
XM_017006778.1:c.3709G=	XP_016862267.1:p.Gly1237=
XM_017006779.1:c.3670G=	XP_016862268.1:p.Gly1224=
XM_017006780.1:c.3670G=	XP_016862269.1:p.Gly1224=
XM_017006783.1:c.3442G=	XP_016862272.1:p.Gly1148=
XM_024453620.1:c.4081G=	XP_024309388.1:p.Gly1361=
XM_024453621.1:c.3757G=	XP_024309389.1:p.Gly1253=
XR_001740195.2:n.8329G=
NM_001080517.3:c.3946G= MANE Select	NP_001073986.1:p.Gly1316=
NM_001292043.2:c.3652G=	NP_001278972.1:p.Gly1218=
NM_001349451.2:c.3652G=	NP_001336380.1:p.Gly1218=