Canonical Allele Identifier: CA2259229312

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727902C= , CM000679.2:g.39727902C=	GRCh38
NC_000017.10:g.37884155C= , CM000679.1:g.37884155C=	GRCh37
NC_000017.9:g.35137681C=	NCBI36
NG_007503.1:g.44763C= , LRG_724:g.44763C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3626C= MANE Select	ENSP00000269571.4:p.Pro1209=
ENST00000269571.9:c.3626C=	ENSP00000269571.4:p.Pro1209=
ENST00000406381.6:c.3536C=	ENSP00000385185.2:p.Pro1179=
ENST00000445658.6:c.2798C=	ENSP00000404047.2:p.Pro933=
ENST00000541774.5:c.3581C=	ENSP00000446466.1:p.Pro1194=
ENST00000578373.5:c.*3416C=	ENSP00000463427.1:n.*3416C=
ENST00000584450.5:c.*205C=	ENSP00000463714.1:n.*205C=
ENST00000584601.5:c.3536C=	ENSP00000462438.1:p.Pro1179=
NM_001005862.2:c.3536C= , LRG_724t1:c.3536C=	NP_001005862.1:p.Pro1179=
NM_001289936.1:c.3581C= , LRG_724t4:c.3581C=	NP_001276865.1:p.Pro1194=
NM_001289937.1:c.*205C=	NP_001276866.1:n.*205C=
NM_004448.3:c.3626C= , LRG_724t2:c.3626C=	NP_004439.2:p.Pro1209=
NR_110535.1:n.3950C=
XM_024450641.1:c.3764C=	XP_024306409.1:p.Pro1255=
XM_024450642.1:c.3719C=	XP_024306410.1:p.Pro1240=
XM_024450643.1:c.3674C=	XP_024306411.1:p.Pro1225=
NM_001005862.3:c.3536C=	NP_001005862.1:p.Pro1179=
NM_001289936.2:c.3581C=	NP_001276865.1:p.Pro1194=
NM_001289937.2:c.*205C=	NP_001276866.1:n.*205C=
NM_001382782.1:c.3536C=	NP_001369711.1:p.Pro1179=
NM_001382783.1:c.3536C=	NP_001369712.1:p.Pro1179=
NM_001382784.1:c.3743C=	NP_001369713.1:p.Pro1248=
NM_001382785.1:c.3728C=	NP_001369714.1:p.Pro1243=
NM_001382786.1:c.3707C=	NP_001369715.1:p.Pro1236=
NM_001382787.1:c.3701C=	NP_001369716.1:p.Pro1234=
NM_001382788.1:c.3656C=	NP_001369717.1:p.Pro1219=
NM_001382789.1:c.3647C=	NP_001369718.1:p.Pro1216=
NM_001382790.1:c.3623C=	NP_001369719.1:p.Pro1208=
NM_001382791.1:c.3617C=	NP_001369720.1:p.Pro1206=
NM_001382792.1:c.3590C=	NP_001369721.1:p.Pro1197=
NM_001382793.1:c.3584C=	NP_001369722.1:p.Pro1195=
NM_001382794.1:c.3584C=	NP_001369723.1:p.Pro1195=
NM_001382795.1:c.3578C=	NP_001369724.1:p.Pro1193=
NM_001382796.1:c.3539C=	NP_001369725.1:p.Pro1180=
NM_001382797.1:c.3527C=	NP_001369726.1:p.Pro1176=
NM_001382798.1:c.3470C=	NP_001369727.1:p.Pro1157=
NM_001382799.1:c.3446C=	NP_001369728.1:p.Pro1149=
NM_001382800.1:c.3440C=	NP_001369729.1:p.Pro1147=
NM_001382801.1:c.3422C=	NP_001369730.1:p.Pro1141=
NM_001382802.1:c.3368C=	NP_001369731.1:p.Pro1123=
NM_001382803.1:c.*205C=	NP_001369732.1:n.*205C=
NM_001382804.1:c.2798C=	NP_001369733.1:p.Pro933=
NM_001382805.1:c.2675C=	NP_001369734.1:p.Pro892=
NM_001382806.1:c.2588C=	NP_001369735.1:p.Pro863=
NM_004448.4:c.3626C= MANE Select	NP_004439.2:p.Pro1209=
NR_110535.2:n.3864C=