Canonical Allele Identifier: CA913012048

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881064_37881065delinsTG (hg19)
• CIViC: CA913012048

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724811_39724812delinsTG , CM000679.2:g.39724811_39724812delinsTG	GRCh38
NC_000017.10:g.37881064_37881065delinsTG , CM000679.1:g.37881064_37881065delinsTG	GRCh37
NC_000017.9:g.35134590_35134591delinsTG	NCBI36
NG_007503.1:g.41672_41673delinsTG , LRG_724:g.41672_41673delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2393_2394delinsTG MANE Select	ENSP00000269571.4:p.Thr798Met
ENST00000269571.9:c.2393_2394delinsTG	ENSP00000269571.4:p.Thr798Met
ENST00000406381.6:c.2303_2304delinsTG	ENSP00000385185.2:p.Thr768Met
ENST00000445658.6:c.1565_1566delinsTG	ENSP00000404047.2:p.Thr522Met
ENST00000541774.5:c.2348_2349delinsTG	ENSP00000446466.1:p.Thr783Met
ENST00000578373.5:c.*2183_*2184delinsTG	ENSP00000463427.1:n.*2183_*2184delinsTG
ENST00000580074.1:c.499_500delinsTG
ENST00000583038.5:n.3527_3528delinsTG
ENST00000584450.5:c.2393_2394delinsTG	ENSP00000463714.1:p.Thr798Met
ENST00000584601.5:c.2303_2304delinsTG	ENSP00000462438.1:p.Thr768Met
NM_001005862.2:c.2303_2304delinsTG , LRG_724t1:c.2303_2304delinsTG	NP_001005862.1:p.Thr768Met
NM_001289936.1:c.2348_2349delinsTG , LRG_724t4:c.2348_2349delinsTG	NP_001276865.1:p.Thr783Met
NM_001289937.1:c.2393_2394delinsTG	NP_001276866.1:p.Thr798Met
NM_004448.3:c.2393_2394delinsTG , LRG_724t2:c.2393_2394delinsTG	NP_004439.2:p.Thr798Met
NR_110535.1:n.2717_2718delinsTG
XM_024450641.1:c.2531_2532delinsTG	XP_024306409.1:p.Thr844Met
XM_024450642.1:c.2486_2487delinsTG	XP_024306410.1:p.Thr829Met
XM_024450643.1:c.2441_2442delinsTG	XP_024306411.1:p.Thr814Met
NM_001005862.3:c.2303_2304delinsTG	NP_001005862.1:p.Thr768Met
NM_001289936.2:c.2348_2349delinsTG	NP_001276865.1:p.Thr783Met
NM_001289937.2:c.2393_2394delinsTG	NP_001276866.1:p.Thr798Met
NM_001382782.1:c.2303_2304delinsTG	NP_001369711.1:p.Thr768Met
NM_001382783.1:c.2303_2304delinsTG	NP_001369712.1:p.Thr768Met
NM_001382784.1:c.2510_2511delinsTG	NP_001369713.1:p.Thr837Met
NM_001382785.1:c.2495_2496delinsTG	NP_001369714.1:p.Thr832Met
NM_001382786.1:c.2474_2475delinsTG	NP_001369715.1:p.Thr825Met
NM_001382787.1:c.2468_2469delinsTG	NP_001369716.1:p.Thr823Met
NM_001382788.1:c.2423_2424delinsTG	NP_001369717.1:p.Thr808Met
NM_001382789.1:c.2414_2415delinsTG	NP_001369718.1:p.Thr805Met
NM_001382790.1:c.2390_2391delinsTG	NP_001369719.1:p.Thr797Met
NM_001382791.1:c.2384_2385delinsTG	NP_001369720.1:p.Thr795Met
NM_001382792.1:c.2357_2358delinsTG	NP_001369721.1:p.Thr786Met
NM_001382793.1:c.2351_2352delinsTG	NP_001369722.1:p.Thr784Met
NM_001382794.1:c.2351_2352delinsTG	NP_001369723.1:p.Thr784Met
NM_001382795.1:c.2345_2346delinsTG	NP_001369724.1:p.Thr782Met
NM_001382796.1:c.2393_2394delinsTG	NP_001369725.1:p.Thr798Met
NM_001382797.1:c.2294_2295delinsTG	NP_001369726.1:p.Thr765Met
NM_001382798.1:c.2393_2394delinsTG	NP_001369727.1:p.Thr798Met
NM_001382799.1:c.2213_2214delinsTG	NP_001369728.1:p.Thr738Met
NM_001382800.1:c.2308-238_2308-237delinsTG	NP_001369729.1:n.2308-238_2308-237delinsTG
NM_001382801.1:c.2345_2346delinsTG	NP_001369730.1:p.Thr782Met
NM_001382802.1:c.2135_2136delinsTG	NP_001369731.1:p.Thr712Met
NM_001382803.1:c.2351_2352delinsTG	NP_001369732.1:p.Thr784Met
NM_001382804.1:c.1565_1566delinsTG	NP_001369733.1:p.Thr522Met
NM_001382805.1:c.2208+1151_2208+1152delinsTG	NP_001369734.1:n.2208+1151_2208+1152delinsTG
NM_001382806.1:c.1355_1356delinsTG	NP_001369735.1:p.Thr452Met
NM_004448.4:c.2393_2394delinsTG MANE Select	NP_004439.2:p.Thr798Met
NR_110535.2:n.2631_2632delinsTG