Canonical Allele Identifier: CA2259227991

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724752C= , CM000679.2:g.39724752C=	GRCh38
NC_000017.10:g.37881005C= , CM000679.1:g.37881005C=	GRCh37
NC_000017.9:g.35134531C=	NCBI36
NG_007503.1:g.41613C= , LRG_724:g.41613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2334C= MANE Select	ENSP00000269571.4:p.Gly778=
ENST00000269571.9:c.2334C=	ENSP00000269571.4:p.Gly778=
ENST00000406381.6:c.2244C=	ENSP00000385185.2:p.Gly748=
ENST00000445658.6:c.1506C=	ENSP00000404047.2:p.Gly502=
ENST00000541774.5:c.2289C=	ENSP00000446466.1:p.Gly763=
ENST00000578373.5:c.*2124C=	ENSP00000463427.1:n.*2124C=
ENST00000580074.1:c.440C=
ENST00000583038.5:n.3468C=
ENST00000584450.5:c.2334C=	ENSP00000463714.1:p.Gly778=
ENST00000584601.5:c.2244C=	ENSP00000462438.1:p.Gly748=
NM_001005862.2:c.2244C= , LRG_724t1:c.2244C=	NP_001005862.1:p.Gly748=
NM_001289936.1:c.2289C= , LRG_724t4:c.2289C=	NP_001276865.1:p.Gly763=
NM_001289937.1:c.2334C=	NP_001276866.1:p.Gly778=
NM_004448.3:c.2334C= , LRG_724t2:c.2334C=	NP_004439.2:p.Gly778=
NR_110535.1:n.2658C=
XM_024450641.1:c.2472C=	XP_024306409.1:p.Gly824=
XM_024450642.1:c.2427C=	XP_024306410.1:p.Gly809=
XM_024450643.1:c.2382C=	XP_024306411.1:p.Gly794=
NM_001005862.3:c.2244C=	NP_001005862.1:p.Gly748=
NM_001289936.2:c.2289C=	NP_001276865.1:p.Gly763=
NM_001289937.2:c.2334C=	NP_001276866.1:p.Gly778=
NM_001382782.1:c.2244C=	NP_001369711.1:p.Gly748=
NM_001382783.1:c.2244C=	NP_001369712.1:p.Gly748=
NM_001382784.1:c.2451C=	NP_001369713.1:p.Gly817=
NM_001382785.1:c.2436C=	NP_001369714.1:p.Gly812=
NM_001382786.1:c.2415C=	NP_001369715.1:p.Gly805=
NM_001382787.1:c.2409C=	NP_001369716.1:p.Gly803=
NM_001382788.1:c.2364C=	NP_001369717.1:p.Gly788=
NM_001382789.1:c.2355C=	NP_001369718.1:p.Gly785=
NM_001382790.1:c.2331C=	NP_001369719.1:p.Gly777=
NM_001382791.1:c.2325C=	NP_001369720.1:p.Gly775=
NM_001382792.1:c.2298C=	NP_001369721.1:p.Gly766=
NM_001382793.1:c.2292C=	NP_001369722.1:p.Gly764=
NM_001382794.1:c.2292C=	NP_001369723.1:p.Gly764=
NM_001382795.1:c.2286C=	NP_001369724.1:p.Gly762=
NM_001382796.1:c.2334C=	NP_001369725.1:p.Gly778=
NM_001382797.1:c.2235C=	NP_001369726.1:p.Gly745=
NM_001382798.1:c.2334C=	NP_001369727.1:p.Gly778=
NM_001382799.1:c.2154C=	NP_001369728.1:p.Gly718=
NM_001382800.1:c.2308-297C=	NP_001369729.1:n.2308-297C=
NM_001382801.1:c.2286C=	NP_001369730.1:p.Gly762=
NM_001382802.1:c.2076C=	NP_001369731.1:p.Gly692=
NM_001382803.1:c.2292C=	NP_001369732.1:p.Gly764=
NM_001382804.1:c.1506C=	NP_001369733.1:p.Gly502=
NM_001382805.1:c.2208+1092C=	NP_001369734.1:n.2208+1092C=
NM_001382806.1:c.1296C=	NP_001369735.1:p.Gly432=
NM_004448.4:c.2334C= MANE Select	NP_004439.2:p.Gly778=
NR_110535.2:n.2572C=