Canonical Allele Identifier: CA2259228820

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727457C= , CM000679.2:g.39727457C=	GRCh38
NC_000017.10:g.37883710C= , CM000679.1:g.37883710C=	GRCh37
NC_000017.9:g.35137236C=	NCBI36
NG_007503.1:g.44318C= , LRG_724:g.44318C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3322C= MANE Select	ENSP00000269571.4:p.Pro1108=
ENST00000269571.9:c.3322C=	ENSP00000269571.4:p.Pro1108=
ENST00000406381.6:c.3232C=	ENSP00000385185.2:p.Pro1078=
ENST00000445658.6:c.2494C=	ENSP00000404047.2:p.Pro832=
ENST00000541774.5:c.3277C=	ENSP00000446466.1:p.Pro1093=
ENST00000578373.5:c.*3112C=	ENSP00000463427.1:n.*3112C=
ENST00000584450.5:c.3160-232C=	ENSP00000463714.1:n.3160-232C=
ENST00000584601.5:c.3232C=	ENSP00000462438.1:p.Pro1078=
NM_001005862.2:c.3232C= , LRG_724t1:c.3232C=	NP_001005862.1:p.Pro1078=
NM_001289936.1:c.3277C= , LRG_724t4:c.3277C=	NP_001276865.1:p.Pro1093=
NM_001289937.1:c.3160-232C=	NP_001276866.1:n.3160-232C=
NM_004448.3:c.3322C= , LRG_724t2:c.3322C=	NP_004439.2:p.Pro1108=
NR_110535.1:n.3646C=
XM_024450641.1:c.3460C=	XP_024306409.1:p.Pro1154=
XM_024450642.1:c.3415C=	XP_024306410.1:p.Pro1139=
XM_024450643.1:c.3370C=	XP_024306411.1:p.Pro1124=
NM_001005862.3:c.3232C=	NP_001005862.1:p.Pro1078=
NM_001289936.2:c.3277C=	NP_001276865.1:p.Pro1093=
NM_001289937.2:c.3160-232C=	NP_001276866.1:n.3160-232C=
NM_001382782.1:c.3232C=	NP_001369711.1:p.Pro1078=
NM_001382783.1:c.3232C=	NP_001369712.1:p.Pro1078=
NM_001382784.1:c.3439C=	NP_001369713.1:p.Pro1147=
NM_001382785.1:c.3424C=	NP_001369714.1:p.Pro1142=
NM_001382786.1:c.3403C=	NP_001369715.1:p.Pro1135=
NM_001382787.1:c.3397C=	NP_001369716.1:p.Pro1133=
NM_001382788.1:c.3352C=	NP_001369717.1:p.Pro1118=
NM_001382789.1:c.3343C=	NP_001369718.1:p.Pro1115=
NM_001382790.1:c.3319C=	NP_001369719.1:p.Pro1107=
NM_001382791.1:c.3313C=	NP_001369720.1:p.Pro1105=
NM_001382792.1:c.3286C=	NP_001369721.1:p.Pro1096=
NM_001382793.1:c.3280C=	NP_001369722.1:p.Pro1094=
NM_001382794.1:c.3280C=	NP_001369723.1:p.Pro1094=
NM_001382795.1:c.3274C=	NP_001369724.1:p.Pro1092=
NM_001382796.1:c.3235C=	NP_001369725.1:p.Pro1079=
NM_001382797.1:c.3223C=	NP_001369726.1:p.Pro1075=
NM_001382798.1:c.3166C=	NP_001369727.1:p.Pro1056=
NM_001382799.1:c.3142C=	NP_001369728.1:p.Pro1048=
NM_001382800.1:c.3136C=	NP_001369729.1:p.Pro1046=
NM_001382801.1:c.3118C=	NP_001369730.1:p.Pro1040=
NM_001382802.1:c.3064C=	NP_001369731.1:p.Pro1022=
NM_001382803.1:c.3118-232C=	NP_001369732.1:n.3118-232C=
NM_001382804.1:c.2494C=	NP_001369733.1:p.Pro832=
NM_001382805.1:c.2371C=	NP_001369734.1:p.Pro791=
NM_001382806.1:c.2284C=	NP_001369735.1:p.Pro762=
NM_004448.4:c.3322C= MANE Select	NP_004439.2:p.Pro1108=
NR_110535.2:n.3560C=