Canonical Allele Identifier: CA2841124910

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724824del , CM000679.2:g.39724824del	GRCh38
NC_000017.10:g.37881077del , CM000679.1:g.37881077del	GRCh37
NC_000017.9:g.35134603del	NCBI36
NG_007503.1:g.41685del , LRG_724:g.41685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2406del MANE Select	ENSP00000269571.4:p.Tyr803MetfsTer5
ENST00000269571.9:c.2406del	ENSP00000269571.4:p.Tyr803MetfsTer5
ENST00000406381.6:c.2316del	ENSP00000385185.2:p.Tyr773MetfsTer5
ENST00000445658.6:c.1578del	ENSP00000404047.2:p.Tyr527MetfsTer5
ENST00000541774.5:c.2361del	ENSP00000446466.1:p.Tyr788MetfsTer5
ENST00000578373.5:c.*2196del	ENSP00000463427.1:n.*2196del
ENST00000580074.1:c.512del
ENST00000583038.5:n.3540del
ENST00000584450.5:c.2406del	ENSP00000463714.1:p.Tyr803MetfsTer5
ENST00000584601.5:c.2316del	ENSP00000462438.1:p.Tyr773MetfsTer5
NM_001005862.2:c.2316del , LRG_724t1:c.2316del	NP_001005862.1:p.Tyr773MetfsTer5
NM_001289936.1:c.2361del , LRG_724t4:c.2361del	NP_001276865.1:p.Tyr788MetfsTer5
NM_001289937.1:c.2406del	NP_001276866.1:p.Tyr803MetfsTer5
NM_004448.3:c.2406del , LRG_724t2:c.2406del	NP_004439.2:p.Tyr803MetfsTer5
NR_110535.1:n.2730del
XM_024450641.1:c.2544del	XP_024306409.1:p.Tyr849MetfsTer5
XM_024450642.1:c.2499del	XP_024306410.1:p.Tyr834MetfsTer5
XM_024450643.1:c.2454del	XP_024306411.1:p.Tyr819MetfsTer5
NM_001005862.3:c.2316del	NP_001005862.1:p.Tyr773MetfsTer5
NM_001289936.2:c.2361del	NP_001276865.1:p.Tyr788MetfsTer5
NM_001289937.2:c.2406del	NP_001276866.1:p.Tyr803MetfsTer5
NM_001382782.1:c.2316del	NP_001369711.1:p.Tyr773MetfsTer5
NM_001382783.1:c.2316del	NP_001369712.1:p.Tyr773MetfsTer5
NM_001382784.1:c.2523del	NP_001369713.1:p.Tyr842MetfsTer5
NM_001382785.1:c.2508del	NP_001369714.1:p.Tyr837MetfsTer5
NM_001382786.1:c.2487del	NP_001369715.1:p.Tyr830MetfsTer5
NM_001382787.1:c.2481del	NP_001369716.1:p.Tyr828MetfsTer5
NM_001382788.1:c.2436del	NP_001369717.1:p.Tyr813MetfsTer5
NM_001382789.1:c.2427del	NP_001369718.1:p.Tyr810MetfsTer5
NM_001382790.1:c.2403del	NP_001369719.1:p.Tyr802MetfsTer5
NM_001382791.1:c.2397del	NP_001369720.1:p.Tyr800MetfsTer5
NM_001382792.1:c.2370del	NP_001369721.1:p.Tyr791MetfsTer5
NM_001382793.1:c.2364del	NP_001369722.1:p.Tyr789MetfsTer5
NM_001382794.1:c.2364del	NP_001369723.1:p.Tyr789MetfsTer5
NM_001382795.1:c.2358del	NP_001369724.1:p.Tyr787MetfsTer5
NM_001382796.1:c.2406del	NP_001369725.1:p.Tyr803MetfsTer5
NM_001382797.1:c.2307del	NP_001369726.1:p.Tyr770MetfsTer5
NM_001382798.1:c.2406del	NP_001369727.1:p.Tyr803MetfsTer5
NM_001382799.1:c.2226del	NP_001369728.1:p.Tyr743MetfsTer5
NM_001382800.1:c.2308-225del	NP_001369729.1:n.2308-225del
NM_001382801.1:c.2358del	NP_001369730.1:p.Tyr787MetfsTer5
NM_001382802.1:c.2148del	NP_001369731.1:p.Tyr717MetfsTer5
NM_001382803.1:c.2364del	NP_001369732.1:p.Tyr789MetfsTer5
NM_001382804.1:c.1578del	NP_001369733.1:p.Tyr527MetfsTer5
NM_001382805.1:c.2208+1164del	NP_001369734.1:n.2208+1164del
NM_001382806.1:c.1368del	NP_001369735.1:p.Tyr457MetfsTer5
NM_004448.4:c.2406del MANE Select	NP_004439.2:p.Tyr803MetfsTer5
NR_110535.2:n.2644del