Canonical Allele Identifier: CA2259222334

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39711931A= , CM000679.2:g.39711931A=	GRCh38
NC_000017.10:g.37868184A= , CM000679.1:g.37868184A=	GRCh37
NC_000017.9:g.35121710A=	NCBI36
NG_007503.1:g.28792A= , LRG_724:g.28792A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.905A= MANE Select	ENSP00000269571.4:p.Asn302=
ENST00000269571.9:c.905A=	ENSP00000269571.4:p.Asn302=
ENST00000406381.6:c.815A=	ENSP00000385185.2:p.Asn272=
ENST00000445658.6:c.77A=	ENSP00000404047.2:p.Asn26=
ENST00000541774.5:c.860A=	ENSP00000446466.1:p.Asn287=
ENST00000578199.5:c.815A=	ENSP00000462808.1:p.Asn272=
ENST00000578373.5:c.*695A=	ENSP00000463427.1:n.*695A=
ENST00000578502.1:c.130A=
ENST00000582648.5:c.229A=	ENSP00000462024.1:p.Thr77=
ENST00000582788.5:n.394A=
ENST00000583038.5:n.1597A=
ENST00000584450.5:c.905A=	ENSP00000463714.1:p.Asn302=
ENST00000584601.5:c.815A=	ENSP00000462438.1:p.Asn272=
ENST00000584908.5:n.917A=
NM_001005862.2:c.815A= , LRG_724t1:c.815A=	NP_001005862.1:p.Asn272=
NM_001289936.1:c.860A= , LRG_724t4:c.860A=	NP_001276865.1:p.Asn287=
NM_001289937.1:c.905A=	NP_001276866.1:p.Asn302=
NM_001289938.1:c.815A= , LRG_724t3:c.815A=	NP_001276867.1:p.Asn272=
NM_004448.3:c.905A= , LRG_724t2:c.905A=	NP_004439.2:p.Asn302=
NR_110535.1:n.1229A=
XM_024450641.1:c.1043A=	XP_024306409.1:p.Asn348=
XM_024450642.1:c.998A=	XP_024306410.1:p.Asn333=
XM_024450643.1:c.953A=	XP_024306411.1:p.Asn318=
NM_001005862.3:c.815A=	NP_001005862.1:p.Asn272=
NM_001289936.2:c.860A=	NP_001276865.1:p.Asn287=
NM_001289937.2:c.905A=	NP_001276866.1:p.Asn302=
NM_001289938.2:c.815A=	NP_001276867.1:p.Asn272=
NM_001382782.1:c.815A=	NP_001369711.1:p.Asn272=
NM_001382783.1:c.815A=	NP_001369712.1:p.Asn272=
NM_001382784.1:c.905A=	NP_001369713.1:p.Asn302=
NM_001382785.1:c.905A=	NP_001369714.1:p.Asn302=
NM_001382786.1:c.905A=	NP_001369715.1:p.Asn302=
NM_001382787.1:c.980A=	NP_001369716.1:p.Asn327=
NM_001382788.1:c.905A=	NP_001369717.1:p.Asn302=
NM_001382789.1:c.905A=	NP_001369718.1:p.Asn302=
NM_001382790.1:c.905A=	NP_001369719.1:p.Asn302=
NM_001382791.1:c.896A=	NP_001369720.1:p.Asn299=
NM_001382792.1:c.905A=	NP_001369721.1:p.Asn302=
NM_001382793.1:c.905A=	NP_001369722.1:p.Asn302=
NM_001382794.1:c.905A=	NP_001369723.1:p.Asn302=
NM_001382795.1:c.905A=	NP_001369724.1:p.Asn302=
NM_001382796.1:c.905A=	NP_001369725.1:p.Asn302=
NM_001382797.1:c.905A=	NP_001369726.1:p.Asn302=
NM_001382798.1:c.905A=	NP_001369727.1:p.Asn302=
NM_001382799.1:c.725A=	NP_001369728.1:p.Asn242=
NM_001382800.1:c.905A=	NP_001369729.1:p.Asn302=
NM_001382801.1:c.905A=	NP_001369730.1:p.Asn302=
NM_001382802.1:c.647A=	NP_001369731.1:p.Asn216=
NM_001382803.1:c.905A=	NP_001369732.1:p.Asn302=
NM_001382804.1:c.77A=	NP_001369733.1:p.Asn26=
NM_001382805.1:c.905A=	NP_001369734.1:p.Asn302=
NM_001382806.1:c.905A=	NP_001369735.1:p.Asn302=
NM_004448.4:c.905A= MANE Select	NP_004439.2:p.Asn302=
NR_110535.2:n.1143A=