Canonical Allele Identifier: CA351692996

Gene: SETD5

Linked Data

• gnomAD v4: 3-9475714-C-T
• MyVariant Identifiers: chr3:g.9517398C>T (hg19) ; chr3:g.9475714C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9475714C>T , CM000665.2:g.9475714C>T	GRCh38
NC_000003.11:g.9517398C>T , CM000665.1:g.9517398C>T	GRCh37
NC_000003.10:g.9492398C>T	NCBI36
NG_034132.1:g.83015C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682236.1:n.2907C>T
ENST00000682536.1:c.4048C>T	ENSP00000507956.1:p.Pro1350Ser
ENST00000687014.1:n.4941C>T
ENST00000689167.1:n.2332C>T
ENST00000693430.1:n.6194C>T
ENST00000402198.7:c.3952C>T MANE Select	ENSP00000385852.2:p.Pro1318Ser
ENST00000663774.1:c.*4098C>T	ENSP00000499452.1:n.*4098C>T
ENST00000665872.1:c.*4021C>T	ENSP00000499600.1:n.*4021C>T
ENST00000666307.1:c.*4326C>T	ENSP00000499402.1:n.*4326C>T
ENST00000670063.1:c.*4057C>T	ENSP00000499725.1:n.*4057C>T
ENST00000302463.10:c.3658C>T	ENSP00000302028.6:p.Pro1220Ser
ENST00000399686.6:c.2722+558C>T
ENST00000402198.5:c.3952C>T	ENSP00000385852.1:p.Pro1318Ser
ENST00000406341.5:c.3952C>T	ENSP00000383939.1:p.Pro1318Ser
ENST00000407969.5:c.4009C>T	ENSP00000384114.1:p.Pro1337Ser
ENST00000413704.5:c.2988C>T
ENST00000466242.5:n.3293C>T
ENST00000493918.5:n.4116C>T
NM_001080517.2:c.3952C>T	NP_001073986.1:p.Pro1318Ser
NM_001292043.1:c.3658C>T	NP_001278972.1:p.Pro1220Ser
XM_005265301.1:c.4009C>T	XP_005265358.1:p.Pro1337Ser
XM_005265303.1:c.3952C>T	XP_005265360.1:p.Pro1318Ser
XM_011533920.1:c.4126C>T	XP_011532222.1:p.Pro1376Ser
XM_011533921.1:c.4126C>T	XP_011532223.1:p.Pro1376Ser
XM_011533922.1:c.4105C>T	XP_011532224.1:p.Pro1369Ser
XM_011533923.1:c.4105C>T	XP_011532225.1:p.Pro1369Ser
XM_011533924.1:c.4105C>T	XP_011532226.1:p.Pro1369Ser
XM_011533925.1:c.4087C>T	XP_011532227.1:p.Pro1363Ser
XM_011533926.1:c.4069C>T	XP_011532228.1:p.Pro1357Ser
XM_011533927.1:c.4069C>T	XP_011532229.1:p.Pro1357Ser
XM_011533928.1:c.4048C>T	XP_011532230.1:p.Pro1350Ser
XM_011533929.1:c.4030C>T	XP_011532231.1:p.Pro1344Ser
XM_011533930.1:c.3991C>T	XP_011532232.1:p.Pro1331Ser
XM_011533931.1:c.3715C>T	XP_011532233.1:p.Pro1239Ser
XM_011533932.1:c.3676C>T	XP_011532234.1:p.Pro1226Ser
XM_011533933.1:c.3676C>T	XP_011532235.1:p.Pro1226Ser
NM_001349451.1:c.3658C>T	NP_001336380.1:p.Pro1220Ser
XM_011533921.2:c.4126C>T	XP_011532223.1:p.Pro1376Ser
XM_017006767.1:c.4126C>T	XP_016862256.1:p.Pro1376Ser
XM_017006768.2:c.4105C>T	XP_016862257.1:p.Pro1369Ser
XM_017006770.1:c.4069C>T	XP_016862259.1:p.Pro1357Ser
XM_017006771.1:c.4066C>T	XP_016862260.1:p.Pro1356Ser
XM_017006772.1:c.4030C>T	XP_016862261.1:p.Pro1344Ser
XM_017006773.1:c.4030C>T	XP_016862262.1:p.Pro1344Ser
XM_017006774.1:c.4009C>T	XP_016862263.1:p.Pro1337Ser
XM_017006775.1:c.3973C>T	XP_016862264.1:p.Pro1325Ser
XM_017006776.1:c.3715C>T	XP_016862265.1:p.Pro1239Ser
XM_017006777.1:c.3715C>T	XP_016862266.1:p.Pro1239Ser
XM_017006778.1:c.3715C>T	XP_016862267.1:p.Pro1239Ser
XM_017006779.1:c.3676C>T	XP_016862268.1:p.Pro1226Ser
XM_017006780.1:c.3676C>T	XP_016862269.1:p.Pro1226Ser
XM_017006783.1:c.3448C>T	XP_016862272.1:p.Pro1150Ser
XM_024453620.1:c.4087C>T	XP_024309388.1:p.Pro1363Ser
XM_024453621.1:c.3763C>T	XP_024309389.1:p.Pro1255Ser
XR_001740195.2:n.8335C>T
NM_001080517.3:c.3952C>T MANE Select	NP_001073986.1:p.Pro1318Ser
NM_001292043.2:c.3658C>T	NP_001278972.1:p.Pro1220Ser
NM_001349451.2:c.3658C>T	NP_001336380.1:p.Pro1220Ser