Canonical Allele Identifier: CA351692723
Gene: SETD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9475694T>C , CM000665.2:g.9475694T>C GRCh38
NC_000003.11:g.9517378T>C , CM000665.1:g.9517378T>C GRCh37
NC_000003.10:g.9492378T>C NCBI36
NG_034132.1:g.82995T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682236.1:n.2887T>C
ENST00000682536.1:c.4028T>C ENSP00000507956.1:p.Leu1343Ser
ENST00000687014.1:n.4921T>C
ENST00000689167.1:n.2312T>C
ENST00000693430.1:n.6174T>C
ENST00000402198.7:c.3932T>C MANE Select ENSP00000385852.2:p.Leu1311Ser
ENST00000663774.1:c.*4078T>C ENSP00000499452.1:n.*4078T>C
ENST00000665872.1:c.*4001T>C ENSP00000499600.1:n.*4001T>C
ENST00000666307.1:c.*4306T>C ENSP00000499402.1:n.*4306T>C
ENST00000670063.1:c.*4037T>C ENSP00000499725.1:n.*4037T>C
ENST00000302463.10:c.3638T>C ENSP00000302028.6:p.Leu1213Ser
ENST00000399686.6:c.2722+538T>C
ENST00000402198.5:c.3932T>C ENSP00000385852.1:p.Leu1311Ser
ENST00000406341.5:c.3932T>C ENSP00000383939.1:p.Leu1311Ser
ENST00000407969.5:c.3989T>C ENSP00000384114.1:p.Leu1330Ser
ENST00000413704.5:c.2968T>C
ENST00000459941.1:n.1063T>C
ENST00000466242.5:n.3273T>C
ENST00000493918.5:n.4096T>C
NM_001080517.2:c.3932T>C NP_001073986.1:p.Leu1311Ser
NM_001292043.1:c.3638T>C NP_001278972.1:p.Leu1213Ser
XM_005265301.1:c.3989T>C XP_005265358.1:p.Leu1330Ser
XM_005265303.1:c.3932T>C XP_005265360.1:p.Leu1311Ser
XM_011533920.1:c.4106T>C XP_011532222.1:p.Leu1369Ser
XM_011533921.1:c.4106T>C XP_011532223.1:p.Leu1369Ser
XM_011533922.1:c.4085T>C XP_011532224.1:p.Leu1362Ser
XM_011533923.1:c.4085T>C XP_011532225.1:p.Leu1362Ser
XM_011533924.1:c.4085T>C XP_011532226.1:p.Leu1362Ser
XM_011533925.1:c.4067T>C XP_011532227.1:p.Leu1356Ser
XM_011533926.1:c.4049T>C XP_011532228.1:p.Leu1350Ser
XM_011533927.1:c.4049T>C XP_011532229.1:p.Leu1350Ser
XM_011533928.1:c.4028T>C XP_011532230.1:p.Leu1343Ser
XM_011533929.1:c.4010T>C XP_011532231.1:p.Leu1337Ser
XM_011533930.1:c.3971T>C XP_011532232.1:p.Leu1324Ser
XM_011533931.1:c.3695T>C XP_011532233.1:p.Leu1232Ser
XM_011533932.1:c.3656T>C XP_011532234.1:p.Leu1219Ser
XM_011533933.1:c.3656T>C XP_011532235.1:p.Leu1219Ser
NM_001349451.1:c.3638T>C NP_001336380.1:p.Leu1213Ser
XM_011533921.2:c.4106T>C XP_011532223.1:p.Leu1369Ser
XM_017006767.1:c.4106T>C XP_016862256.1:p.Leu1369Ser
XM_017006768.2:c.4085T>C XP_016862257.1:p.Leu1362Ser
XM_017006770.1:c.4049T>C XP_016862259.1:p.Leu1350Ser
XM_017006771.1:c.4046T>C XP_016862260.1:p.Leu1349Ser
XM_017006772.1:c.4010T>C XP_016862261.1:p.Leu1337Ser
XM_017006773.1:c.4010T>C XP_016862262.1:p.Leu1337Ser
XM_017006774.1:c.3989T>C XP_016862263.1:p.Leu1330Ser
XM_017006775.1:c.3953T>C XP_016862264.1:p.Leu1318Ser
XM_017006776.1:c.3695T>C XP_016862265.1:p.Leu1232Ser
XM_017006777.1:c.3695T>C XP_016862266.1:p.Leu1232Ser
XM_017006778.1:c.3695T>C XP_016862267.1:p.Leu1232Ser
XM_017006779.1:c.3656T>C XP_016862268.1:p.Leu1219Ser
XM_017006780.1:c.3656T>C XP_016862269.1:p.Leu1219Ser
XM_017006783.1:c.3428T>C XP_016862272.1:p.Leu1143Ser
XM_024453620.1:c.4067T>C XP_024309388.1:p.Leu1356Ser
XM_024453621.1:c.3743T>C XP_024309389.1:p.Leu1248Ser
XR_001740195.2:n.8315T>C
NM_001080517.3:c.3932T>C MANE Select NP_001073986.1:p.Leu1311Ser
NM_001292043.2:c.3638T>C NP_001278972.1:p.Leu1213Ser
NM_001349451.2:c.3638T>C NP_001336380.1:p.Leu1213Ser