Canonical Allele Identifier: CA351690725

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9517191A>T (hg19) ; chr3:g.9475507A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475507A>T , CM000665.2:g.9475507A>T	GRCh38
NC_000003.11:g.9517191A>T , CM000665.1:g.9517191A>T	GRCh37
NC_000003.10:g.9492191A>T	NCBI36
NG_034132.1:g.82808A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2700A>T
ENST00000682536.1:c.3841A>T	ENSP00000507956.1:p.Thr1281Ser
ENST00000687014.1:n.4734A>T
ENST00000689167.1:n.2125A>T
ENST00000691925.1:n.6542A>T
ENST00000693430.1:n.5987A>T
ENST00000402198.7:c.3745A>T MANE Select	ENSP00000385852.2:p.Thr1249Ser
ENST00000663774.1:c.*3891A>T	ENSP00000499452.1:n.*3891A>T
ENST00000665872.1:c.*3814A>T	ENSP00000499600.1:n.*3814A>T
ENST00000666307.1:c.*4119A>T	ENSP00000499402.1:n.*4119A>T
ENST00000670063.1:c.*3850A>T	ENSP00000499725.1:n.*3850A>T
ENST00000302463.10:c.3451A>T	ENSP00000302028.6:p.Thr1151Ser
ENST00000399686.6:c.2722+351A>T
ENST00000402198.5:c.3745A>T	ENSP00000385852.1:p.Thr1249Ser
ENST00000406341.5:c.3745A>T	ENSP00000383939.1:p.Thr1249Ser
ENST00000407969.5:c.3802A>T	ENSP00000384114.1:p.Thr1268Ser
ENST00000413704.5:c.2781A>T
ENST00000459941.1:n.876A>T
ENST00000466242.5:n.3086A>T
ENST00000466826.1:n.132A>T
ENST00000493918.5:n.3909A>T
NM_001080517.2:c.3745A>T	NP_001073986.1:p.Thr1249Ser
NM_001292043.1:c.3451A>T	NP_001278972.1:p.Thr1151Ser
XM_005265301.1:c.3802A>T	XP_005265358.1:p.Thr1268Ser
XM_005265303.1:c.3745A>T	XP_005265360.1:p.Thr1249Ser
XM_011533920.1:c.3919A>T	XP_011532222.1:p.Thr1307Ser
XM_011533921.1:c.3919A>T	XP_011532223.1:p.Thr1307Ser
XM_011533922.1:c.3898A>T	XP_011532224.1:p.Thr1300Ser
XM_011533923.1:c.3898A>T	XP_011532225.1:p.Thr1300Ser
XM_011533924.1:c.3898A>T	XP_011532226.1:p.Thr1300Ser
XM_011533925.1:c.3880A>T	XP_011532227.1:p.Thr1294Ser
XM_011533926.1:c.3862A>T	XP_011532228.1:p.Thr1288Ser
XM_011533927.1:c.3862A>T	XP_011532229.1:p.Thr1288Ser
XM_011533928.1:c.3841A>T	XP_011532230.1:p.Thr1281Ser
XM_011533929.1:c.3823A>T	XP_011532231.1:p.Thr1275Ser
XM_011533930.1:c.3784A>T	XP_011532232.1:p.Thr1262Ser
XM_011533931.1:c.3508A>T	XP_011532233.1:p.Thr1170Ser
XM_011533932.1:c.3469A>T	XP_011532234.1:p.Thr1157Ser
XM_011533933.1:c.3469A>T	XP_011532235.1:p.Thr1157Ser
NM_001349451.1:c.3451A>T	NP_001336380.1:p.Thr1151Ser
XM_011533921.2:c.3919A>T	XP_011532223.1:p.Thr1307Ser
XM_017006767.1:c.3919A>T	XP_016862256.1:p.Thr1307Ser
XM_017006768.2:c.3898A>T	XP_016862257.1:p.Thr1300Ser
XM_017006770.1:c.3862A>T	XP_016862259.1:p.Thr1288Ser
XM_017006771.1:c.3859A>T	XP_016862260.1:p.Thr1287Ser
XM_017006772.1:c.3823A>T	XP_016862261.1:p.Thr1275Ser
XM_017006773.1:c.3823A>T	XP_016862262.1:p.Thr1275Ser
XM_017006774.1:c.3802A>T	XP_016862263.1:p.Thr1268Ser
XM_017006775.1:c.3766A>T	XP_016862264.1:p.Thr1256Ser
XM_017006776.1:c.3508A>T	XP_016862265.1:p.Thr1170Ser
XM_017006777.1:c.3508A>T	XP_016862266.1:p.Thr1170Ser
XM_017006778.1:c.3508A>T	XP_016862267.1:p.Thr1170Ser
XM_017006779.1:c.3469A>T	XP_016862268.1:p.Thr1157Ser
XM_017006780.1:c.3469A>T	XP_016862269.1:p.Thr1157Ser
XM_017006783.1:c.3241A>T	XP_016862272.1:p.Thr1081Ser
XM_024453620.1:c.3880A>T	XP_024309388.1:p.Thr1294Ser
XM_024453621.1:c.3556A>T	XP_024309389.1:p.Thr1186Ser
XR_001740195.2:n.8128A>T
NM_001080517.3:c.3745A>T MANE Select	NP_001073986.1:p.Thr1249Ser
NM_001292043.2:c.3451A>T	NP_001278972.1:p.Thr1151Ser
NM_001349451.2:c.3451A>T	NP_001336380.1:p.Thr1151Ser