Canonical Allele Identifier: CA433602102

Gene: SETD2

Linked Data

• dbSNP Id: rs2106674017
• gnomAD v4: 3-47122275-T-C
• MyVariant Identifiers: chr3:g.47163765T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47122275T>C , CM000665.2:g.47122275T>C	GRCh38
NC_000003.11:g.47163765T>C , CM000665.1:g.47163765T>C	GRCh37
NC_000003.10:g.47138769T>C	NCBI36
NG_032091.1:g.46703A>G , LRG_775:g.46703A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638947.2:c.2229A>G	ENSP00000491413.2:p.Lys743=
ENST00000685005.1:c.2262A>G	ENSP00000509568.1:p.Lys754=
ENST00000685399.1:c.241A>G
ENST00000685505.1:c.302A>G
ENST00000686773.1:c.241A>G
ENST00000688290.1:c.241A>G
ENST00000690461.1:c.525A>G	ENSP00000509352.1:p.Lys175=
ENST00000691544.1:c.72-24194A>G	ENSP00000510710.1:n.72-24194A>G
ENST00000692883.1:c.302A>G
ENST00000693321.1:c.241A>G
ENST00000409792.4:c.2361A>G MANE Select	ENSP00000386759.3:p.Lys787=
ENST00000330022.11:c.1976A>G
ENST00000409792.3:c.2361A>G	ENSP00000386759.3:p.Lys787=
ENST00000412450.1:c.2229A>G	ENSP00000416401.1:p.Lys743=
ENST00000431180.5:c.1513A>G
ENST00000445387.5:c.1261A>G
NM_014159.6:c.2361A>G , LRG_775t1:c.2361A>G	NP_054878.5:p.Lys787=
XM_011533631.1:c.2439A>G	XP_011531933.1:p.Lys813=
XM_011533632.1:c.2385A>G	XP_011531934.1:p.Lys795=
XM_011533633.1:c.2439A>G	XP_011531935.1:p.Lys813=
XM_011533634.1:c.2229A>G	XP_011531936.1:p.Lys743=
XR_940418.1:n.2454A>G
XR_940419.1:n.2542A>G
XR_940420.1:n.2542A>G
NM_001349370.1:c.2229A>G	NP_001336299.1:p.Lys743=
NR_146158.1:n.2414A>G
XM_011533632.3:c.2385A>G	XP_011531934.1:p.Lys795=
XM_024453487.1:c.2229A>G	XP_024309255.1:p.Lys743=
XM_024453488.1:c.2229A>G	XP_024309256.1:p.Lys743=
XM_024453489.1:c.2229A>G	XP_024309257.1:p.Lys743=
XR_001740131.2:n.2414A>G
XR_002959510.1:n.2290A>G
XR_002959511.1:n.2290A>G
XR_002959512.1:n.2290A>G
XR_002959513.1:n.2290A>G
XR_002959514.1:n.2290A>G
XR_002959515.1:n.2290A>G
XR_002959516.1:n.2290A>G
XR_002959517.1:n.2290A>G
NM_001349370.2:c.2229A>G	NP_001336299.1:p.Lys743=
NR_146158.2:n.2550A>G
NM_001349370.3:c.2229A>G	NP_001336299.1:p.Lys743=
NM_014159.7:c.2361A>G MANE Select	NP_054878.5:p.Lys787=
NR_146158.3:n.2550A>G