Canonical Allele Identifier: CA351691553

Gene: SETD5

Linked Data

• MyVariant Identifiers: chr3:g.9517291G>T (hg19) ; chr3:g.9475607G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475607G>T , CM000665.2:g.9475607G>T	GRCh38
NC_000003.11:g.9517291G>T , CM000665.1:g.9517291G>T	GRCh37
NC_000003.10:g.9492291G>T	NCBI36
NG_034132.1:g.82908G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682236.1:n.2800G>T
ENST00000682536.1:c.3941G>T	ENSP00000507956.1:p.Gly1314Val
ENST00000687014.1:n.4834G>T
ENST00000689167.1:n.2225G>T
ENST00000691925.1:n.6642G>T
ENST00000693430.1:n.6087G>T
ENST00000402198.7:c.3845G>T MANE Select	ENSP00000385852.2:p.Gly1282Val
ENST00000663774.1:c.*3991G>T	ENSP00000499452.1:n.*3991G>T
ENST00000665872.1:c.*3914G>T	ENSP00000499600.1:n.*3914G>T
ENST00000666307.1:c.*4219G>T	ENSP00000499402.1:n.*4219G>T
ENST00000670063.1:c.*3950G>T	ENSP00000499725.1:n.*3950G>T
ENST00000302463.10:c.3551G>T	ENSP00000302028.6:p.Gly1184Val
ENST00000399686.6:c.2722+451G>T
ENST00000402198.5:c.3845G>T	ENSP00000385852.1:p.Gly1282Val
ENST00000406341.5:c.3845G>T	ENSP00000383939.1:p.Gly1282Val
ENST00000407969.5:c.3902G>T	ENSP00000384114.1:p.Gly1301Val
ENST00000413704.5:c.2881G>T
ENST00000459941.1:n.976G>T
ENST00000466242.5:n.3186G>T
ENST00000466826.1:n.232G>T
ENST00000493918.5:n.4009G>T
NM_001080517.2:c.3845G>T	NP_001073986.1:p.Gly1282Val
NM_001292043.1:c.3551G>T	NP_001278972.1:p.Gly1184Val
XM_005265301.1:c.3902G>T	XP_005265358.1:p.Gly1301Val
XM_005265303.1:c.3845G>T	XP_005265360.1:p.Gly1282Val
XM_011533920.1:c.4019G>T	XP_011532222.1:p.Gly1340Val
XM_011533921.1:c.4019G>T	XP_011532223.1:p.Gly1340Val
XM_011533922.1:c.3998G>T	XP_011532224.1:p.Gly1333Val
XM_011533923.1:c.3998G>T	XP_011532225.1:p.Gly1333Val
XM_011533924.1:c.3998G>T	XP_011532226.1:p.Gly1333Val
XM_011533925.1:c.3980G>T	XP_011532227.1:p.Gly1327Val
XM_011533926.1:c.3962G>T	XP_011532228.1:p.Gly1321Val
XM_011533927.1:c.3962G>T	XP_011532229.1:p.Gly1321Val
XM_011533928.1:c.3941G>T	XP_011532230.1:p.Gly1314Val
XM_011533929.1:c.3923G>T	XP_011532231.1:p.Gly1308Val
XM_011533930.1:c.3884G>T	XP_011532232.1:p.Gly1295Val
XM_011533931.1:c.3608G>T	XP_011532233.1:p.Gly1203Val
XM_011533932.1:c.3569G>T	XP_011532234.1:p.Gly1190Val
XM_011533933.1:c.3569G>T	XP_011532235.1:p.Gly1190Val
NM_001349451.1:c.3551G>T	NP_001336380.1:p.Gly1184Val
XM_011533921.2:c.4019G>T	XP_011532223.1:p.Gly1340Val
XM_017006767.1:c.4019G>T	XP_016862256.1:p.Gly1340Val
XM_017006768.2:c.3998G>T	XP_016862257.1:p.Gly1333Val
XM_017006770.1:c.3962G>T	XP_016862259.1:p.Gly1321Val
XM_017006771.1:c.3959G>T	XP_016862260.1:p.Gly1320Val
XM_017006772.1:c.3923G>T	XP_016862261.1:p.Gly1308Val
XM_017006773.1:c.3923G>T	XP_016862262.1:p.Gly1308Val
XM_017006774.1:c.3902G>T	XP_016862263.1:p.Gly1301Val
XM_017006775.1:c.3866G>T	XP_016862264.1:p.Gly1289Val
XM_017006776.1:c.3608G>T	XP_016862265.1:p.Gly1203Val
XM_017006777.1:c.3608G>T	XP_016862266.1:p.Gly1203Val
XM_017006778.1:c.3608G>T	XP_016862267.1:p.Gly1203Val
XM_017006779.1:c.3569G>T	XP_016862268.1:p.Gly1190Val
XM_017006780.1:c.3569G>T	XP_016862269.1:p.Gly1190Val
XM_017006783.1:c.3341G>T	XP_016862272.1:p.Gly1114Val
XM_024453620.1:c.3980G>T	XP_024309388.1:p.Gly1327Val
XM_024453621.1:c.3656G>T	XP_024309389.1:p.Gly1219Val
XR_001740195.2:n.8228G>T
NM_001080517.3:c.3845G>T MANE Select	NP_001073986.1:p.Gly1282Val
NM_001292043.2:c.3551G>T	NP_001278972.1:p.Gly1184Val
NM_001349451.2:c.3551G>T	NP_001336380.1:p.Gly1184Val