Canonical Allele Identifier: CA2259229302

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727886G= , CM000679.2:g.39727886G=	GRCh38
NC_000017.10:g.37884139G= , CM000679.1:g.37884139G=	GRCh37
NC_000017.9:g.35137665G=	NCBI36
NG_007503.1:g.44747G= , LRG_724:g.44747G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3610G= MANE Select	ENSP00000269571.4:p.Ala1204=
ENST00000269571.9:c.3610G=	ENSP00000269571.4:p.Ala1204=
ENST00000406381.6:c.3520G=	ENSP00000385185.2:p.Ala1174=
ENST00000445658.6:c.2782G=	ENSP00000404047.2:p.Ala928=
ENST00000541774.5:c.3565G=	ENSP00000446466.1:p.Ala1189=
ENST00000578373.5:c.*3400G=	ENSP00000463427.1:n.*3400G=
ENST00000584450.5:c.*189G=	ENSP00000463714.1:n.*189G=
ENST00000584601.5:c.3520G=	ENSP00000462438.1:p.Ala1174=
NM_001005862.2:c.3520G= , LRG_724t1:c.3520G=	NP_001005862.1:p.Ala1174=
NM_001289936.1:c.3565G= , LRG_724t4:c.3565G=	NP_001276865.1:p.Ala1189=
NM_001289937.1:c.*189G=	NP_001276866.1:n.*189G=
NM_004448.3:c.3610G= , LRG_724t2:c.3610G=	NP_004439.2:p.Ala1204=
NR_110535.1:n.3934G=
XM_024450641.1:c.3748G=	XP_024306409.1:p.Ala1250=
XM_024450642.1:c.3703G=	XP_024306410.1:p.Ala1235=
XM_024450643.1:c.3658G=	XP_024306411.1:p.Ala1220=
NM_001005862.3:c.3520G=	NP_001005862.1:p.Ala1174=
NM_001289936.2:c.3565G=	NP_001276865.1:p.Ala1189=
NM_001289937.2:c.*189G=	NP_001276866.1:n.*189G=
NM_001382782.1:c.3520G=	NP_001369711.1:p.Ala1174=
NM_001382783.1:c.3520G=	NP_001369712.1:p.Ala1174=
NM_001382784.1:c.3727G=	NP_001369713.1:p.Ala1243=
NM_001382785.1:c.3712G=	NP_001369714.1:p.Ala1238=
NM_001382786.1:c.3691G=	NP_001369715.1:p.Ala1231=
NM_001382787.1:c.3685G=	NP_001369716.1:p.Ala1229=
NM_001382788.1:c.3640G=	NP_001369717.1:p.Ala1214=
NM_001382789.1:c.3631G=	NP_001369718.1:p.Ala1211=
NM_001382790.1:c.3607G=	NP_001369719.1:p.Ala1203=
NM_001382791.1:c.3601G=	NP_001369720.1:p.Ala1201=
NM_001382792.1:c.3574G=	NP_001369721.1:p.Ala1192=
NM_001382793.1:c.3568G=	NP_001369722.1:p.Ala1190=
NM_001382794.1:c.3568G=	NP_001369723.1:p.Ala1190=
NM_001382795.1:c.3562G=	NP_001369724.1:p.Ala1188=
NM_001382796.1:c.3523G=	NP_001369725.1:p.Ala1175=
NM_001382797.1:c.3511G=	NP_001369726.1:p.Ala1171=
NM_001382798.1:c.3454G=	NP_001369727.1:p.Ala1152=
NM_001382799.1:c.3430G=	NP_001369728.1:p.Ala1144=
NM_001382800.1:c.3424G=	NP_001369729.1:p.Ala1142=
NM_001382801.1:c.3406G=	NP_001369730.1:p.Ala1136=
NM_001382802.1:c.3352G=	NP_001369731.1:p.Ala1118=
NM_001382803.1:c.*189G=	NP_001369732.1:n.*189G=
NM_001382804.1:c.2782G=	NP_001369733.1:p.Ala928=
NM_001382805.1:c.2659G=	NP_001369734.1:p.Ala887=
NM_001382806.1:c.2572G=	NP_001369735.1:p.Ala858=
NM_004448.4:c.3610G= MANE Select	NP_004439.2:p.Ala1204=
NR_110535.2:n.3848G=