Canonical Allele Identifier: CA1344742651

Gene: SETD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475685C= , CM000665.2:g.9475685C=	GRCh38
NC_000003.11:g.9517369C= , CM000665.1:g.9517369C=	GRCh37
NC_000003.10:g.9492369C=	NCBI36
NG_034132.1:g.82986C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2878C=
ENST00000682536.1:c.4019C=	ENSP00000507956.1:p.Thr1340=
ENST00000687014.1:n.4912C=
ENST00000689167.1:n.2303C=
ENST00000693430.1:n.6165C=
ENST00000402198.7:c.3923C= MANE Select	ENSP00000385852.2:p.Thr1308=
ENST00000663774.1:c.*4069C=	ENSP00000499452.1:n.*4069C=
ENST00000665872.1:c.*3992C=	ENSP00000499600.1:n.*3992C=
ENST00000666307.1:c.*4297C=	ENSP00000499402.1:n.*4297C=
ENST00000670063.1:c.*4028C=	ENSP00000499725.1:n.*4028C=
ENST00000302463.10:c.3629C=	ENSP00000302028.6:p.Thr1210=
ENST00000399686.6:c.2722+529C=
ENST00000402198.5:c.3923C=	ENSP00000385852.1:p.Thr1308=
ENST00000406341.5:c.3923C=	ENSP00000383939.1:p.Thr1308=
ENST00000407969.5:c.3980C=	ENSP00000384114.1:p.Thr1327=
ENST00000413704.5:c.2959C=
ENST00000459941.1:n.1054C=
ENST00000466242.5:n.3264C=
ENST00000493918.5:n.4087C=
NM_001080517.2:c.3923C=	NP_001073986.1:p.Thr1308=
NM_001292043.1:c.3629C=	NP_001278972.1:p.Thr1210=
XM_005265301.1:c.3980C=	XP_005265358.1:p.Thr1327=
XM_005265303.1:c.3923C=	XP_005265360.1:p.Thr1308=
XM_011533920.1:c.4097C=	XP_011532222.1:p.Thr1366=
XM_011533921.1:c.4097C=	XP_011532223.1:p.Thr1366=
XM_011533922.1:c.4076C=	XP_011532224.1:p.Thr1359=
XM_011533923.1:c.4076C=	XP_011532225.1:p.Thr1359=
XM_011533924.1:c.4076C=	XP_011532226.1:p.Thr1359=
XM_011533925.1:c.4058C=	XP_011532227.1:p.Thr1353=
XM_011533926.1:c.4040C=	XP_011532228.1:p.Thr1347=
XM_011533927.1:c.4040C=	XP_011532229.1:p.Thr1347=
XM_011533928.1:c.4019C=	XP_011532230.1:p.Thr1340=
XM_011533929.1:c.4001C=	XP_011532231.1:p.Thr1334=
XM_011533930.1:c.3962C=	XP_011532232.1:p.Thr1321=
XM_011533931.1:c.3686C=	XP_011532233.1:p.Thr1229=
XM_011533932.1:c.3647C=	XP_011532234.1:p.Thr1216=
XM_011533933.1:c.3647C=	XP_011532235.1:p.Thr1216=
NM_001349451.1:c.3629C=	NP_001336380.1:p.Thr1210=
XM_011533921.2:c.4097C=	XP_011532223.1:p.Thr1366=
XM_017006767.1:c.4097C=	XP_016862256.1:p.Thr1366=
XM_017006768.2:c.4076C=	XP_016862257.1:p.Thr1359=
XM_017006770.1:c.4040C=	XP_016862259.1:p.Thr1347=
XM_017006771.1:c.4037C=	XP_016862260.1:p.Thr1346=
XM_017006772.1:c.4001C=	XP_016862261.1:p.Thr1334=
XM_017006773.1:c.4001C=	XP_016862262.1:p.Thr1334=
XM_017006774.1:c.3980C=	XP_016862263.1:p.Thr1327=
XM_017006775.1:c.3944C=	XP_016862264.1:p.Thr1315=
XM_017006776.1:c.3686C=	XP_016862265.1:p.Thr1229=
XM_017006777.1:c.3686C=	XP_016862266.1:p.Thr1229=
XM_017006778.1:c.3686C=	XP_016862267.1:p.Thr1229=
XM_017006779.1:c.3647C=	XP_016862268.1:p.Thr1216=
XM_017006780.1:c.3647C=	XP_016862269.1:p.Thr1216=
XM_017006783.1:c.3419C=	XP_016862272.1:p.Thr1140=
XM_024453620.1:c.4058C=	XP_024309388.1:p.Thr1353=
XM_024453621.1:c.3734C=	XP_024309389.1:p.Thr1245=
XR_001740195.2:n.8306C=
NM_001080517.3:c.3923C= MANE Select	NP_001073986.1:p.Thr1308=
NM_001292043.2:c.3629C=	NP_001278972.1:p.Thr1210=
NM_001349451.2:c.3629C=	NP_001336380.1:p.Thr1210=