Canonical Allele Identifier: CA1344742507

Gene: SETD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475617_9475618delinsCT , CM000665.2:g.9475617_9475618delinsCT	GRCh38
NC_000003.11:g.9517301_9517302delinsCT , CM000665.1:g.9517301_9517302delinsCT	GRCh37
NC_000003.10:g.9492301_9492302delinsCT	NCBI36
NG_034132.1:g.82918_82919delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682236.1:n.2810_2811delinsCT
ENST00000682536.1:c.3951_3952delinsCT	ENSP00000507956.1:p.Pro1317=
ENST00000687014.1:n.4844_4845delinsCT
ENST00000689167.1:n.2235_2236delinsCT
ENST00000691925.1:n.6652_6653delinsCT
ENST00000693430.1:n.6097_6098delinsCT
ENST00000402198.7:c.3855_3856delinsCT MANE Select	ENSP00000385852.2:p.Pro1285=
ENST00000663774.1:c.*4001_*4002delinsCT	ENSP00000499452.1:n.*4001_*4002delinsCT
ENST00000665872.1:c.*3924_*3925delinsCT	ENSP00000499600.1:n.*3924_*3925delinsCT
ENST00000666307.1:c.*4229_*4230delinsCT	ENSP00000499402.1:n.*4229_*4230delinsCT
ENST00000670063.1:c.*3960_*3961delinsCT	ENSP00000499725.1:n.*3960_*3961delinsCT
ENST00000302463.10:c.3561_3562delinsCT	ENSP00000302028.6:p.Pro1187=
ENST00000399686.6:c.2722+461_2722+462delinsCT
ENST00000402198.5:c.3855_3856delinsCT	ENSP00000385852.1:p.Pro1285=
ENST00000406341.5:c.3855_3856delinsCT	ENSP00000383939.1:p.Pro1285=
ENST00000407969.5:c.3912_3913delinsCT	ENSP00000384114.1:p.Pro1304=
ENST00000413704.5:c.2891_2892delinsCT
ENST00000459941.1:n.986_987delinsCT
ENST00000466242.5:n.3196_3197delinsCT
ENST00000466826.1:n.242_243delinsCT
ENST00000493918.5:n.4019_4020delinsCT
NM_001080517.2:c.3855_3856delinsCT	NP_001073986.1:p.Pro1285=
NM_001292043.1:c.3561_3562delinsCT	NP_001278972.1:p.Pro1187=
XM_005265301.1:c.3912_3913delinsCT	XP_005265358.1:p.Pro1304=
XM_005265303.1:c.3855_3856delinsCT	XP_005265360.1:p.Pro1285=
XM_011533920.1:c.4029_4030delinsCT	XP_011532222.1:p.Pro1343=
XM_011533921.1:c.4029_4030delinsCT	XP_011532223.1:p.Pro1343=
XM_011533922.1:c.4008_4009delinsCT	XP_011532224.1:p.Pro1336=
XM_011533923.1:c.4008_4009delinsCT	XP_011532225.1:p.Pro1336=
XM_011533924.1:c.4008_4009delinsCT	XP_011532226.1:p.Pro1336=
XM_011533925.1:c.3990_3991delinsCT	XP_011532227.1:p.Pro1330=
XM_011533926.1:c.3972_3973delinsCT	XP_011532228.1:p.Pro1324=
XM_011533927.1:c.3972_3973delinsCT	XP_011532229.1:p.Pro1324=
XM_011533928.1:c.3951_3952delinsCT	XP_011532230.1:p.Pro1317=
XM_011533929.1:c.3933_3934delinsCT	XP_011532231.1:p.Pro1311=
XM_011533930.1:c.3894_3895delinsCT	XP_011532232.1:p.Pro1298=
XM_011533931.1:c.3618_3619delinsCT	XP_011532233.1:p.Pro1206=
XM_011533932.1:c.3579_3580delinsCT	XP_011532234.1:p.Pro1193=
XM_011533933.1:c.3579_3580delinsCT	XP_011532235.1:p.Pro1193=
NM_001349451.1:c.3561_3562delinsCT	NP_001336380.1:p.Pro1187=
XM_011533921.2:c.4029_4030delinsCT	XP_011532223.1:p.Pro1343=
XM_017006767.1:c.4029_4030delinsCT	XP_016862256.1:p.Pro1343=
XM_017006768.2:c.4008_4009delinsCT	XP_016862257.1:p.Pro1336=
XM_017006770.1:c.3972_3973delinsCT	XP_016862259.1:p.Pro1324=
XM_017006771.1:c.3969_3970delinsCT	XP_016862260.1:p.Pro1323=
XM_017006772.1:c.3933_3934delinsCT	XP_016862261.1:p.Pro1311=
XM_017006773.1:c.3933_3934delinsCT	XP_016862262.1:p.Pro1311=
XM_017006774.1:c.3912_3913delinsCT	XP_016862263.1:p.Pro1304=
XM_017006775.1:c.3876_3877delinsCT	XP_016862264.1:p.Pro1292=
XM_017006776.1:c.3618_3619delinsCT	XP_016862265.1:p.Pro1206=
XM_017006777.1:c.3618_3619delinsCT	XP_016862266.1:p.Pro1206=
XM_017006778.1:c.3618_3619delinsCT	XP_016862267.1:p.Pro1206=
XM_017006779.1:c.3579_3580delinsCT	XP_016862268.1:p.Pro1193=
XM_017006780.1:c.3579_3580delinsCT	XP_016862269.1:p.Pro1193=
XM_017006783.1:c.3351_3352delinsCT	XP_016862272.1:p.Pro1117=
XM_024453620.1:c.3990_3991delinsCT	XP_024309388.1:p.Pro1330=
XM_024453621.1:c.3666_3667delinsCT	XP_024309389.1:p.Pro1222=
XR_001740195.2:n.8238_8239delinsCT
NM_001080517.3:c.3855_3856delinsCT MANE Select	NP_001073986.1:p.Pro1285=
NM_001292043.2:c.3561_3562delinsCT	NP_001278972.1:p.Pro1187=
NM_001349451.2:c.3561_3562delinsCT	NP_001336380.1:p.Pro1187=