Canonical Allele Identifier: CA162110

Gene: SETD2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47120443A>G , CM000665.2:g.47120443A>G	GRCh38
NC_000003.11:g.47161933A>G , CM000665.1:g.47161933A>G	GRCh37
NC_000003.10:g.47136937A>G	NCBI36
NG_032091.1:g.48535T>C , LRG_775:g.48535T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014159.7:c.4193T>C MANE Select	NP_054878.5:p.Ile1398Thr
ENST00000409792.4:c.4193T>C MANE Select	ENSP00000386759.3:p.Ile1398Thr
NM_001349370.1:c.4061T>C	NP_001336299.1:p.Ile1354Thr
NM_001349370.2:c.4061T>C	NP_001336299.1:p.Ile1354Thr
NM_001349370.3:c.4061T>C	NP_001336299.1:p.Ile1354Thr
NM_014159.6:c.4193T>C , LRG_775t1:c.4193T>C	NP_054878.5:p.Ile1398Thr
NR_146158.1:n.4246T>C
NR_146158.2:n.4382T>C
NR_146158.3:n.4382T>C
ENST00000330022.11:c.3808T>C
ENST00000409792.3:c.4193T>C	ENSP00000386759.3:p.Ile1398Thr
ENST00000431180.5:c.3345T>C
ENST00000445387.5:c.3093T>C
ENST00000638947.2:c.4061T>C	ENSP00000491413.2:p.Ile1354Thr
ENST00000685005.1:c.4094T>C	ENSP00000509568.1:p.Ile1365Thr
ENST00000685399.1:c.2073T>C
ENST00000685505.1:c.2134T>C
ENST00000686773.1:c.2073T>C
ENST00000686876.1:c.1209T>C
ENST00000688290.1:c.2073T>C
ENST00000690157.1:c.1209T>C
ENST00000690461.1:c.2357T>C	ENSP00000509352.1:p.Ile786Thr
ENST00000691544.1:c.72-22362T>C	ENSP00000510710.1:n.72-22362T>C
ENST00000691902.1:c.1209T>C
ENST00000692883.1:c.2134T>C
ENST00000693321.1:c.2073T>C
XM_011533631.1:c.4271T>C	XP_011531933.1:p.Ile1424Thr
XM_011533632.1:c.4217T>C	XP_011531934.1:p.Ile1406Thr
XM_011533632.3:c.4217T>C	XP_011531934.1:p.Ile1406Thr
XM_011533633.1:c.4271T>C	XP_011531935.1:p.Ile1424Thr
XM_011533634.1:c.4061T>C	XP_011531936.1:p.Ile1354Thr
XM_024453487.1:c.4061T>C	XP_024309255.1:p.Ile1354Thr
XM_024453488.1:c.4061T>C	XP_024309256.1:p.Ile1354Thr
XM_024453489.1:c.4061T>C	XP_024309257.1:p.Ile1354Thr
XR_001740131.2:n.4246T>C
XR_002959510.1:n.4122T>C
XR_002959511.1:n.4122T>C
XR_002959512.1:n.4122T>C
XR_002959513.1:n.4122T>C
XR_002959514.1:n.4122T>C
XR_002959515.1:n.4122T>C
XR_002959516.1:n.4122T>C
XR_002959517.1:n.4122T>C
XR_940418.1:n.4286T>C
XR_940419.1:n.4374T>C
XR_940420.1:n.4374T>C