Canonical Allele Identifier: CA2259229263

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727795C= , CM000679.2:g.39727795C=	GRCh38
NC_000017.10:g.37884048C= , CM000679.1:g.37884048C=	GRCh37
NC_000017.9:g.35137574C=	NCBI36
NG_007503.1:g.44656C= , LRG_724:g.44656C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.3519C= MANE Select	ENSP00000269571.4:p.Leu1173=
ENST00000269571.9:c.3519C=	ENSP00000269571.4:p.Leu1173=
ENST00000406381.6:c.3429C=	ENSP00000385185.2:p.Leu1143=
ENST00000445658.6:c.2691C=	ENSP00000404047.2:p.Leu897=
ENST00000541774.5:c.3474C=	ENSP00000446466.1:p.Leu1158=
ENST00000578373.5:c.*3309C=	ENSP00000463427.1:n.*3309C=
ENST00000584450.5:c.*98C=	ENSP00000463714.1:n.*98C=
ENST00000584601.5:c.3429C=	ENSP00000462438.1:p.Leu1143=
NM_001005862.2:c.3429C= , LRG_724t1:c.3429C=	NP_001005862.1:p.Leu1143=
NM_001289936.1:c.3474C= , LRG_724t4:c.3474C=	NP_001276865.1:p.Leu1158=
NM_001289937.1:c.*98C=	NP_001276866.1:n.*98C=
NM_004448.3:c.3519C= , LRG_724t2:c.3519C=	NP_004439.2:p.Leu1173=
NR_110535.1:n.3843C=
XM_024450641.1:c.3657C=	XP_024306409.1:p.Leu1219=
XM_024450642.1:c.3612C=	XP_024306410.1:p.Leu1204=
XM_024450643.1:c.3567C=	XP_024306411.1:p.Leu1189=
NM_001005862.3:c.3429C=	NP_001005862.1:p.Leu1143=
NM_001289936.2:c.3474C=	NP_001276865.1:p.Leu1158=
NM_001289937.2:c.*98C=	NP_001276866.1:n.*98C=
NM_001382782.1:c.3429C=	NP_001369711.1:p.Leu1143=
NM_001382783.1:c.3429C=	NP_001369712.1:p.Leu1143=
NM_001382784.1:c.3636C=	NP_001369713.1:p.Leu1212=
NM_001382785.1:c.3621C=	NP_001369714.1:p.Leu1207=
NM_001382786.1:c.3600C=	NP_001369715.1:p.Leu1200=
NM_001382787.1:c.3594C=	NP_001369716.1:p.Leu1198=
NM_001382788.1:c.3549C=	NP_001369717.1:p.Leu1183=
NM_001382789.1:c.3540C=	NP_001369718.1:p.Leu1180=
NM_001382790.1:c.3516C=	NP_001369719.1:p.Leu1172=
NM_001382791.1:c.3510C=	NP_001369720.1:p.Leu1170=
NM_001382792.1:c.3483C=	NP_001369721.1:p.Leu1161=
NM_001382793.1:c.3477C=	NP_001369722.1:p.Leu1159=
NM_001382794.1:c.3477C=	NP_001369723.1:p.Leu1159=
NM_001382795.1:c.3471C=	NP_001369724.1:p.Leu1157=
NM_001382796.1:c.3432C=	NP_001369725.1:p.Leu1144=
NM_001382797.1:c.3420C=	NP_001369726.1:p.Leu1140=
NM_001382798.1:c.3363C=	NP_001369727.1:p.Leu1121=
NM_001382799.1:c.3339C=	NP_001369728.1:p.Leu1113=
NM_001382800.1:c.3333C=	NP_001369729.1:p.Leu1111=
NM_001382801.1:c.3315C=	NP_001369730.1:p.Leu1105=
NM_001382802.1:c.3261C=	NP_001369731.1:p.Leu1087=
NM_001382803.1:c.*98C=	NP_001369732.1:n.*98C=
NM_001382804.1:c.2691C=	NP_001369733.1:p.Leu897=
NM_001382805.1:c.2568C=	NP_001369734.1:p.Leu856=
NM_001382806.1:c.2481C=	NP_001369735.1:p.Leu827=
NM_004448.4:c.3519C= MANE Select	NP_004439.2:p.Leu1173=
NR_110535.2:n.3757C=