Canonical Allele Identifier: CA10639626

Gene: STAT3

Linked Data

• ClinVar Variation Id: 323216
• ClinVar RCV Id: RCV000372678
• dbSNP Id: rs886052934
• gnomAD v4: 17-42314070-A-G
• MyVariant Identifiers: chr17:g.40466088A>G (hg19) ; chr17:g.42314070A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42314070A>G , CM000679.2:g.42314070A>G	GRCh38
NC_000017.10:g.40466088A>G , CM000679.1:g.40466088A>G	GRCh37
NC_000017.9:g.37719614A>G	NCBI36
NG_007370.1:g.79426T>C , LRG_112:g.79426T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713583.1:c.*1675T>C	ENSP00000518875.1:n.*1675T>C
ENST00000264657.10:c.*1675T>C MANE Select	ENSP00000264657.4:n.*1675T>C
ENST00000676636.1:c.*2327T>C	ENSP00000504255.1:n.*2327T>C
ENST00000677030.1:c.*1769T>C	ENSP00000503662.1:n.*1769T>C
ENST00000677271.1:c.*2326T>C	ENSP00000503912.1:n.*2326T>C
ENST00000677421.1:c.*1675T>C	ENSP00000503599.1:n.*1675T>C
ENST00000677442.1:c.*1675T>C	ENSP00000504350.1:n.*1675T>C
ENST00000677479.1:c.*1769T>C	ENSP00000503559.1:n.*1769T>C
ENST00000677723.1:c.*1675T>C	ENSP00000503574.1:n.*1675T>C
ENST00000677820.1:c.*2330T>C	ENSP00000504715.1:n.*2330T>C
ENST00000678043.1:c.*1675T>C	ENSP00000503872.1:n.*1675T>C
ENST00000678044.1:c.*1675T>C	ENSP00000503102.1:n.*1675T>C
ENST00000678048.1:c.*1675T>C	ENSP00000503799.1:n.*1675T>C
ENST00000678445.1:c.*2380T>C	ENSP00000503105.1:n.*2380T>C
ENST00000678572.1:c.*1769T>C	ENSP00000504182.1:n.*1769T>C
ENST00000678674.1:c.*1675T>C	ENSP00000504062.1:n.*1675T>C
ENST00000678764.1:n.4405T>C
ENST00000678792.1:c.*1675T>C	ENSP00000504435.1:n.*1675T>C
ENST00000678827.1:c.*1769T>C	ENSP00000503634.1:n.*1769T>C
ENST00000678905.1:c.*1769T>C	ENSP00000503333.1:n.*1769T>C
ENST00000678906.1:c.*1675T>C	ENSP00000504184.1:n.*1675T>C
ENST00000678913.1:c.*1675T>C	ENSP00000504609.1:n.*1675T>C
ENST00000678960.1:c.*1675T>C	ENSP00000503181.1:n.*1675T>C
ENST00000679014.1:c.*1675T>C	ENSP00000503237.1:n.*1675T>C
ENST00000679166.1:c.*1675T>C	ENSP00000503308.1:n.*1675T>C
ENST00000679185.1:c.*1769T>C	ENSP00000503332.1:n.*1769T>C
ENST00000679231.1:n.4231T>C
ENST00000264657.9:c.*1675T>C	ENSP00000264657.4:n.*1675T>C
NM_003150.3:c.*1675T>C	NP_003141.2:n.*1675T>C
NM_139276.2:c.*1675T>C , LRG_112t1:c.*1675T>C	NP_644805.1:n.*1675T>C
NM_213662.1:c.*1769T>C	NP_998827.1:n.*1769T>C
XM_005257616.2:c.*1675T>C	XP_005257673.2:n.*1675T>C
XM_005257617.2:c.*1675T>C	XP_005257674.2:n.*1675T>C
XM_011525145.1:c.*1675T>C	XP_011523447.1:n.*1675T>C
XM_011525146.1:c.*1769T>C	XP_011523448.1:n.*1769T>C
XM_011525145.3:c.*1675T>C	XP_011523447.1:n.*1675T>C
XM_011525146.3:c.*1769T>C	XP_011523448.1:n.*1769T>C
XM_017024973.2:c.*1769T>C	XP_016880462.1:n.*1769T>C
NM_001369512.1:c.*1675T>C	NP_001356441.1:n.*1675T>C
NM_001369513.1:c.*1675T>C	NP_001356442.1:n.*1675T>C
NM_001369514.1:c.*1675T>C	NP_001356443.1:n.*1675T>C
NM_001369516.1:c.*1675T>C	NP_001356445.1:n.*1675T>C
NM_001369517.1:c.*1769T>C	NP_001356446.1:n.*1769T>C
NM_001369518.1:c.*1769T>C	NP_001356447.1:n.*1769T>C
NM_001369519.1:c.*1769T>C	NP_001356448.1:n.*1769T>C
NM_001369520.1:c.*1769T>C	NP_001356449.1:n.*1769T>C
NM_003150.4:c.*1675T>C	NP_003141.2:n.*1675T>C
NM_213662.2:c.*1769T>C	NP_998827.1:n.*1769T>C
NM_001384984.1:c.*1675T>C	NP_001371913.1:n.*1675T>C
NM_001384985.1:c.*1675T>C	NP_001371914.1:n.*1675T>C
NM_001384986.1:c.*1769T>C	NP_001371915.1:n.*1769T>C
NM_001384987.1:c.*1675T>C	NP_001371916.1:n.*1675T>C
NM_001384988.1:c.*1675T>C	NP_001371917.1:n.*1675T>C
NM_001384989.1:c.*1675T>C	NP_001371918.1:n.*1675T>C
NM_001384990.1:c.*1769T>C	NP_001371919.1:n.*1769T>C
NM_001384991.1:c.*1675T>C	NP_001371920.1:n.*1675T>C
NM_001384992.1:c.*1675T>C	NP_001371921.1:n.*1675T>C
NM_001384993.1:c.*1675T>C	NP_001371922.1:n.*1675T>C
NM_139276.3:c.*1675T>C MANE Select	NP_644805.1:n.*1675T>C