Canonical Allele Identifier: CA351691046

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9517235A>T (hg19) ; chr3:g.9475551A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475551A>T , CM000665.2:g.9475551A>T	GRCh38
NC_000003.11:g.9517235A>T , CM000665.1:g.9517235A>T	GRCh37
NC_000003.10:g.9492235A>T	NCBI36
NG_034132.1:g.82852A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2744A>T
ENST00000682536.1:c.3885A>T	ENSP00000507956.1:p.Arg1295Ser
ENST00000687014.1:n.4778A>T
ENST00000689167.1:n.2169A>T
ENST00000691925.1:n.6586A>T
ENST00000693430.1:n.6031A>T
ENST00000402198.7:c.3789A>T MANE Select	ENSP00000385852.2:p.Arg1263Ser
ENST00000663774.1:c.*3935A>T	ENSP00000499452.1:n.*3935A>T
ENST00000665872.1:c.*3858A>T	ENSP00000499600.1:n.*3858A>T
ENST00000666307.1:c.*4163A>T	ENSP00000499402.1:n.*4163A>T
ENST00000670063.1:c.*3894A>T	ENSP00000499725.1:n.*3894A>T
ENST00000302463.10:c.3495A>T	ENSP00000302028.6:p.Arg1165Ser
ENST00000399686.6:c.2722+395A>T
ENST00000402198.5:c.3789A>T	ENSP00000385852.1:p.Arg1263Ser
ENST00000406341.5:c.3789A>T	ENSP00000383939.1:p.Arg1263Ser
ENST00000407969.5:c.3846A>T	ENSP00000384114.1:p.Arg1282Ser
ENST00000413704.5:c.2825A>T
ENST00000459941.1:n.920A>T
ENST00000466242.5:n.3130A>T
ENST00000466826.1:n.176A>T
ENST00000493918.5:n.3953A>T
NM_001080517.2:c.3789A>T	NP_001073986.1:p.Arg1263Ser
NM_001292043.1:c.3495A>T	NP_001278972.1:p.Arg1165Ser
XM_005265301.1:c.3846A>T	XP_005265358.1:p.Arg1282Ser
XM_005265303.1:c.3789A>T	XP_005265360.1:p.Arg1263Ser
XM_011533920.1:c.3963A>T	XP_011532222.1:p.Arg1321Ser
XM_011533921.1:c.3963A>T	XP_011532223.1:p.Arg1321Ser
XM_011533922.1:c.3942A>T	XP_011532224.1:p.Arg1314Ser
XM_011533923.1:c.3942A>T	XP_011532225.1:p.Arg1314Ser
XM_011533924.1:c.3942A>T	XP_011532226.1:p.Arg1314Ser
XM_011533925.1:c.3924A>T	XP_011532227.1:p.Arg1308Ser
XM_011533926.1:c.3906A>T	XP_011532228.1:p.Arg1302Ser
XM_011533927.1:c.3906A>T	XP_011532229.1:p.Arg1302Ser
XM_011533928.1:c.3885A>T	XP_011532230.1:p.Arg1295Ser
XM_011533929.1:c.3867A>T	XP_011532231.1:p.Arg1289Ser
XM_011533930.1:c.3828A>T	XP_011532232.1:p.Arg1276Ser
XM_011533931.1:c.3552A>T	XP_011532233.1:p.Arg1184Ser
XM_011533932.1:c.3513A>T	XP_011532234.1:p.Arg1171Ser
XM_011533933.1:c.3513A>T	XP_011532235.1:p.Arg1171Ser
NM_001349451.1:c.3495A>T	NP_001336380.1:p.Arg1165Ser
XM_011533921.2:c.3963A>T	XP_011532223.1:p.Arg1321Ser
XM_017006767.1:c.3963A>T	XP_016862256.1:p.Arg1321Ser
XM_017006768.2:c.3942A>T	XP_016862257.1:p.Arg1314Ser
XM_017006770.1:c.3906A>T	XP_016862259.1:p.Arg1302Ser
XM_017006771.1:c.3903A>T	XP_016862260.1:p.Arg1301Ser
XM_017006772.1:c.3867A>T	XP_016862261.1:p.Arg1289Ser
XM_017006773.1:c.3867A>T	XP_016862262.1:p.Arg1289Ser
XM_017006774.1:c.3846A>T	XP_016862263.1:p.Arg1282Ser
XM_017006775.1:c.3810A>T	XP_016862264.1:p.Arg1270Ser
XM_017006776.1:c.3552A>T	XP_016862265.1:p.Arg1184Ser
XM_017006777.1:c.3552A>T	XP_016862266.1:p.Arg1184Ser
XM_017006778.1:c.3552A>T	XP_016862267.1:p.Arg1184Ser
XM_017006779.1:c.3513A>T	XP_016862268.1:p.Arg1171Ser
XM_017006780.1:c.3513A>T	XP_016862269.1:p.Arg1171Ser
XM_017006783.1:c.3285A>T	XP_016862272.1:p.Arg1095Ser
XM_024453620.1:c.3924A>T	XP_024309388.1:p.Arg1308Ser
XM_024453621.1:c.3600A>T	XP_024309389.1:p.Arg1200Ser
XR_001740195.2:n.8172A>T
NM_001080517.3:c.3789A>T MANE Select	NP_001073986.1:p.Arg1263Ser
NM_001292043.2:c.3495A>T	NP_001278972.1:p.Arg1165Ser
NM_001349451.2:c.3495A>T	NP_001336380.1:p.Arg1165Ser