Canonical Allele Identifier: CA2259228025

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724842C= , CM000679.2:g.39724842C=	GRCh38
NC_000017.10:g.37881095C= , CM000679.1:g.37881095C=	GRCh37
NC_000017.9:g.35134621C=	NCBI36
NG_007503.1:g.41703C= , LRG_724:g.41703C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2424C= MANE Select	ENSP00000269571.4:p.Asp808=
ENST00000269571.9:c.2424C=	ENSP00000269571.4:p.Asp808=
ENST00000406381.6:c.2334C=	ENSP00000385185.2:p.Asp778=
ENST00000445658.6:c.1596C=	ENSP00000404047.2:p.Asp532=
ENST00000541774.5:c.2379C=	ENSP00000446466.1:p.Asp793=
ENST00000578373.5:c.*2214C=	ENSP00000463427.1:n.*2214C=
ENST00000580074.1:c.530C=
ENST00000583038.5:n.3558C=
ENST00000584450.5:c.2424C=	ENSP00000463714.1:p.Asp808=
ENST00000584601.5:c.2334C=	ENSP00000462438.1:p.Asp778=
NM_001005862.2:c.2334C= , LRG_724t1:c.2334C=	NP_001005862.1:p.Asp778=
NM_001289936.1:c.2379C= , LRG_724t4:c.2379C=	NP_001276865.1:p.Asp793=
NM_001289937.1:c.2424C=	NP_001276866.1:p.Asp808=
NM_004448.3:c.2424C= , LRG_724t2:c.2424C=	NP_004439.2:p.Asp808=
NR_110535.1:n.2748C=
XM_024450641.1:c.2562C=	XP_024306409.1:p.Asp854=
XM_024450642.1:c.2517C=	XP_024306410.1:p.Asp839=
XM_024450643.1:c.2472C=	XP_024306411.1:p.Asp824=
NM_001005862.3:c.2334C=	NP_001005862.1:p.Asp778=
NM_001289936.2:c.2379C=	NP_001276865.1:p.Asp793=
NM_001289937.2:c.2424C=	NP_001276866.1:p.Asp808=
NM_001382782.1:c.2334C=	NP_001369711.1:p.Asp778=
NM_001382783.1:c.2334C=	NP_001369712.1:p.Asp778=
NM_001382784.1:c.2541C=	NP_001369713.1:p.Asp847=
NM_001382785.1:c.2526C=	NP_001369714.1:p.Asp842=
NM_001382786.1:c.2505C=	NP_001369715.1:p.Asp835=
NM_001382787.1:c.2499C=	NP_001369716.1:p.Asp833=
NM_001382788.1:c.2454C=	NP_001369717.1:p.Asp818=
NM_001382789.1:c.2445C=	NP_001369718.1:p.Asp815=
NM_001382790.1:c.2421C=	NP_001369719.1:p.Asp807=
NM_001382791.1:c.2415C=	NP_001369720.1:p.Asp805=
NM_001382792.1:c.2388C=	NP_001369721.1:p.Asp796=
NM_001382793.1:c.2382C=	NP_001369722.1:p.Asp794=
NM_001382794.1:c.2382C=	NP_001369723.1:p.Asp794=
NM_001382795.1:c.2376C=	NP_001369724.1:p.Asp792=
NM_001382796.1:c.2424C=	NP_001369725.1:p.Asp808=
NM_001382797.1:c.2325C=	NP_001369726.1:p.Asp775=
NM_001382798.1:c.2424C=	NP_001369727.1:p.Asp808=
NM_001382799.1:c.2244C=	NP_001369728.1:p.Asp748=
NM_001382800.1:c.2308-207C=	NP_001369729.1:n.2308-207C=
NM_001382801.1:c.2376C=	NP_001369730.1:p.Asp792=
NM_001382802.1:c.2166C=	NP_001369731.1:p.Asp722=
NM_001382803.1:c.2382C=	NP_001369732.1:p.Asp794=
NM_001382804.1:c.1596C=	NP_001369733.1:p.Asp532=
NM_001382805.1:c.2208+1182C=	NP_001369734.1:n.2208+1182C=
NM_001382806.1:c.1386C=	NP_001369735.1:p.Asp462=
NM_004448.4:c.2424C= MANE Select	NP_004439.2:p.Asp808=
NR_110535.2:n.2662C=