Canonical Allele Identifier: CA2579784385
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724744_39724745insTTG , CM000679.2:g.39724744_39724745insTTG GRCh38
NC_000017.10:g.37880997_37880998insTTG , CM000679.1:g.37880997_37880998insTTG GRCh37
NC_000017.9:g.35134523_35134524insTTG NCBI36
NG_007503.1:g.41605_41606insTTG , LRG_724:g.41605_41606insTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000269571.10:c.2326_2327insTTG MANE Select ENSP00000269571.4:p.Ala775_Gly776insVal
ENST00000269571.9:c.2326_2327insTTG ENSP00000269571.4:p.Ala775_Gly776insVal
ENST00000406381.6:c.2236_2237insTTG ENSP00000385185.2:p.Ala745_Gly746insVal
ENST00000445658.6:c.1498_1499insTTG ENSP00000404047.2:p.Ala499_Gly500insVal
ENST00000541774.5:c.2281_2282insTTG ENSP00000446466.1:p.Ala760_Gly761insVal
ENST00000578373.5:c.*2116_*2117insTTG ENSP00000463427.1:n.*2116_*2117insTTG
ENST00000580074.1:c.432_433insTTG
ENST00000583038.5:n.3460_3461insTTG
ENST00000584450.5:c.2326_2327insTTG ENSP00000463714.1:p.Ala775_Gly776insVal
ENST00000584601.5:c.2236_2237insTTG ENSP00000462438.1:p.Ala745_Gly746insVal
NM_001005862.2:c.2236_2237insTTG , LRG_724t1:c.2236_2237insTTG NP_001005862.1:p.Ala745_Gly746insVal
NM_001289936.1:c.2281_2282insTTG , LRG_724t4:c.2281_2282insTTG NP_001276865.1:p.Ala760_Gly761insVal
NM_001289937.1:c.2326_2327insTTG NP_001276866.1:p.Ala775_Gly776insVal
NM_004448.3:c.2326_2327insTTG , LRG_724t2:c.2326_2327insTTG NP_004439.2:p.Ala775_Gly776insVal
NR_110535.1:n.2650_2651insTTG
XM_024450641.1:c.2464_2465insTTG XP_024306409.1:p.Ala821_Gly822insVal
XM_024450642.1:c.2419_2420insTTG XP_024306410.1:p.Ala806_Gly807insVal
XM_024450643.1:c.2374_2375insTTG XP_024306411.1:p.Ala791_Gly792insVal
NM_001005862.3:c.2236_2237insTTG NP_001005862.1:p.Ala745_Gly746insVal
NM_001289936.2:c.2281_2282insTTG NP_001276865.1:p.Ala760_Gly761insVal
NM_001289937.2:c.2326_2327insTTG NP_001276866.1:p.Ala775_Gly776insVal
NM_001382782.1:c.2236_2237insTTG NP_001369711.1:p.Ala745_Gly746insVal
NM_001382783.1:c.2236_2237insTTG NP_001369712.1:p.Ala745_Gly746insVal
NM_001382784.1:c.2443_2444insTTG NP_001369713.1:p.Ala814_Gly815insVal
NM_001382785.1:c.2428_2429insTTG NP_001369714.1:p.Ala809_Gly810insVal
NM_001382786.1:c.2407_2408insTTG NP_001369715.1:p.Ala802_Gly803insVal
NM_001382787.1:c.2401_2402insTTG NP_001369716.1:p.Ala800_Gly801insVal
NM_001382788.1:c.2356_2357insTTG NP_001369717.1:p.Ala785_Gly786insVal
NM_001382789.1:c.2347_2348insTTG NP_001369718.1:p.Ala782_Gly783insVal
NM_001382790.1:c.2323_2324insTTG NP_001369719.1:p.Ala774_Gly775insVal
NM_001382791.1:c.2317_2318insTTG NP_001369720.1:p.Ala772_Gly773insVal
NM_001382792.1:c.2290_2291insTTG NP_001369721.1:p.Ala763_Gly764insVal
NM_001382793.1:c.2284_2285insTTG NP_001369722.1:p.Ala761_Gly762insVal
NM_001382794.1:c.2284_2285insTTG NP_001369723.1:p.Ala761_Gly762insVal
NM_001382795.1:c.2278_2279insTTG NP_001369724.1:p.Ala759_Gly760insVal
NM_001382796.1:c.2326_2327insTTG NP_001369725.1:p.Ala775_Gly776insVal
NM_001382797.1:c.2227_2228insTTG NP_001369726.1:p.Ala742_Gly743insVal
NM_001382798.1:c.2326_2327insTTG NP_001369727.1:p.Ala775_Gly776insVal
NM_001382799.1:c.2146_2147insTTG NP_001369728.1:p.Ala715_Gly716insVal
NM_001382800.1:c.2308-305_2308-304insTTG NP_001369729.1:n.2308-305_2308-304insTTG
NM_001382801.1:c.2278_2279insTTG NP_001369730.1:p.Ala759_Gly760insVal
NM_001382802.1:c.2068_2069insTTG NP_001369731.1:p.Ala689_Gly690insVal
NM_001382803.1:c.2284_2285insTTG NP_001369732.1:p.Ala761_Gly762insVal
NM_001382804.1:c.1498_1499insTTG NP_001369733.1:p.Ala499_Gly500insVal
NM_001382805.1:c.2208+1084_2208+1085insTTG NP_001369734.1:n.2208+1084_2208+1085insTT...
NM_001382806.1:c.1288_1289insTTG NP_001369735.1:p.Ala429_Gly430insVal
NM_004448.4:c.2326_2327insTTG MANE Select NP_004439.2:p.Ala775_Gly776insVal
NR_110535.2:n.2564_2565insTTG