Canonical Allele Identifier: CA2259227976

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724734_39724744delinsCGTGATGGCTG , CM000679.2:g.39724734_39724744delinsCGTGATGGCTG	GRCh38
NC_000017.10:g.37880987_37880997delinsCGTGATGGCTG , CM000679.1:g.37880987_37880997delinsCGTGATGGCTG	GRCh37
NC_000017.9:g.35134513_35134523delinsCGTGATGGCTG	NCBI36
NG_007503.1:g.41595_41605delinsCGTGATGGCTG , LRG_724:g.41595_41605delinsCGTGATGGCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2316_2326delinsCGTGATGGCTG MANE Select	ENSP00000269571.4:p.Tyr772=
ENST00000269571.9:c.2316_2326delinsCGTGATGGCTG	ENSP00000269571.4:p.Tyr772=
ENST00000406381.6:c.2226_2236delinsCGTGATGGCTG	ENSP00000385185.2:p.Tyr742=
ENST00000445658.6:c.1488_1498delinsCGTGATGGCTG	ENSP00000404047.2:p.Tyr496=
ENST00000541774.5:c.2271_2281delinsCGTGATGGCTG	ENSP00000446466.1:p.Tyr757=
ENST00000578373.5:c.*2106_*2116delinsCGTGATGGCTG	ENSP00000463427.1:n.*2106_*2116delinsCGTG...
ENST00000580074.1:c.422_432delinsCGTGATGGCTG
ENST00000583038.5:n.3450_3460delinsCGTGATGGCTG
ENST00000584450.5:c.2316_2326delinsCGTGATGGCTG	ENSP00000463714.1:p.Tyr772=
ENST00000584601.5:c.2226_2236delinsCGTGATGGCTG	ENSP00000462438.1:p.Tyr742=
NM_001005862.2:c.2226_2236delinsCGTGATGGCTG , LRG_724t1:c.2226_2236delinsCGTGATGGCTG	NP_001005862.1:p.Tyr742=
NM_001289936.1:c.2271_2281delinsCGTGATGGCTG , LRG_724t4:c.2271_2281delinsCGTGATGGCTG	NP_001276865.1:p.Tyr757=
NM_001289937.1:c.2316_2326delinsCGTGATGGCTG	NP_001276866.1:p.Tyr772=
NM_004448.3:c.2316_2326delinsCGTGATGGCTG , LRG_724t2:c.2316_2326delinsCGTGATGGCTG	NP_004439.2:p.Tyr772=
NR_110535.1:n.2640_2650delinsCGTGATGGCTG
XM_024450641.1:c.2454_2464delinsCGTGATGGCTG	XP_024306409.1:p.Tyr818=
XM_024450642.1:c.2409_2419delinsCGTGATGGCTG	XP_024306410.1:p.Tyr803=
XM_024450643.1:c.2364_2374delinsCGTGATGGCTG	XP_024306411.1:p.Tyr788=
NM_001005862.3:c.2226_2236delinsCGTGATGGCTG	NP_001005862.1:p.Tyr742=
NM_001289936.2:c.2271_2281delinsCGTGATGGCTG	NP_001276865.1:p.Tyr757=
NM_001289937.2:c.2316_2326delinsCGTGATGGCTG	NP_001276866.1:p.Tyr772=
NM_001382782.1:c.2226_2236delinsCGTGATGGCTG	NP_001369711.1:p.Tyr742=
NM_001382783.1:c.2226_2236delinsCGTGATGGCTG	NP_001369712.1:p.Tyr742=
NM_001382784.1:c.2433_2443delinsCGTGATGGCTG	NP_001369713.1:p.Tyr811=
NM_001382785.1:c.2418_2428delinsCGTGATGGCTG	NP_001369714.1:p.Tyr806=
NM_001382786.1:c.2397_2407delinsCGTGATGGCTG	NP_001369715.1:p.Tyr799=
NM_001382787.1:c.2391_2401delinsCGTGATGGCTG	NP_001369716.1:p.Tyr797=
NM_001382788.1:c.2346_2356delinsCGTGATGGCTG	NP_001369717.1:p.Tyr782=
NM_001382789.1:c.2337_2347delinsCGTGATGGCTG	NP_001369718.1:p.Tyr779=
NM_001382790.1:c.2313_2323delinsCGTGATGGCTG	NP_001369719.1:p.Tyr771=
NM_001382791.1:c.2307_2317delinsCGTGATGGCTG	NP_001369720.1:p.Tyr769=
NM_001382792.1:c.2280_2290delinsCGTGATGGCTG	NP_001369721.1:p.Tyr760=
NM_001382793.1:c.2274_2284delinsCGTGATGGCTG	NP_001369722.1:p.Tyr758=
NM_001382794.1:c.2274_2284delinsCGTGATGGCTG	NP_001369723.1:p.Tyr758=
NM_001382795.1:c.2268_2278delinsCGTGATGGCTG	NP_001369724.1:p.Tyr756=
NM_001382796.1:c.2316_2326delinsCGTGATGGCTG	NP_001369725.1:p.Tyr772=
NM_001382797.1:c.2217_2227delinsCGTGATGGCTG	NP_001369726.1:p.Tyr739=
NM_001382798.1:c.2316_2326delinsCGTGATGGCTG	NP_001369727.1:p.Tyr772=
NM_001382799.1:c.2136_2146delinsCGTGATGGCTG	NP_001369728.1:p.Tyr712=
NM_001382800.1:c.2308-315_2308-305delinsCGTGATGGCTG	NP_001369729.1:n.2308-315_2308-305delinsC...
NM_001382801.1:c.2268_2278delinsCGTGATGGCTG	NP_001369730.1:p.Tyr756=
NM_001382802.1:c.2058_2068delinsCGTGATGGCTG	NP_001369731.1:p.Tyr686=
NM_001382803.1:c.2274_2284delinsCGTGATGGCTG	NP_001369732.1:p.Tyr758=
NM_001382804.1:c.1488_1498delinsCGTGATGGCTG	NP_001369733.1:p.Tyr496=
NM_001382805.1:c.2208+1074_2208+1084delinsCGTGATGGCTG	NP_001369734.1:n.2208+1074_2208+1084delin...
NM_001382806.1:c.1278_1288delinsCGTGATGGCTG	NP_001369735.1:p.Tyr426=
NM_004448.4:c.2316_2326delinsCGTGATGGCTG MANE Select	NP_004439.2:p.Tyr772=
NR_110535.2:n.2554_2564delinsCGTGATGGCTG