Canonical Allele Identifier: CA2259228797

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727429G= , CM000679.2:g.39727429G=	GRCh38
NC_000017.10:g.37883682G= , CM000679.1:g.37883682G=	GRCh37
NC_000017.9:g.35137208G=	NCBI36
NG_007503.1:g.44290G= , LRG_724:g.44290G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3294G= MANE Select	ENSP00000269571.4:p.Leu1098=
ENST00000269571.9:c.3294G=	ENSP00000269571.4:p.Leu1098=
ENST00000406381.6:c.3204G=	ENSP00000385185.2:p.Leu1068=
ENST00000445658.6:c.2466G=	ENSP00000404047.2:p.Leu822=
ENST00000541774.5:c.3249G=	ENSP00000446466.1:p.Leu1083=
ENST00000578373.5:c.*3084G=	ENSP00000463427.1:n.*3084G=
ENST00000584450.5:c.3160-260G=	ENSP00000463714.1:n.3160-260G=
ENST00000584601.5:c.3204G=	ENSP00000462438.1:p.Leu1068=
NM_001005862.2:c.3204G= , LRG_724t1:c.3204G=	NP_001005862.1:p.Leu1068=
NM_001289936.1:c.3249G= , LRG_724t4:c.3249G=	NP_001276865.1:p.Leu1083=
NM_001289937.1:c.3160-260G=	NP_001276866.1:n.3160-260G=
NM_004448.3:c.3294G= , LRG_724t2:c.3294G=	NP_004439.2:p.Leu1098=
NR_110535.1:n.3618G=
XM_024450641.1:c.3432G=	XP_024306409.1:p.Leu1144=
XM_024450642.1:c.3387G=	XP_024306410.1:p.Leu1129=
XM_024450643.1:c.3342G=	XP_024306411.1:p.Leu1114=
NM_001005862.3:c.3204G=	NP_001005862.1:p.Leu1068=
NM_001289936.2:c.3249G=	NP_001276865.1:p.Leu1083=
NM_001289937.2:c.3160-260G=	NP_001276866.1:n.3160-260G=
NM_001382782.1:c.3204G=	NP_001369711.1:p.Leu1068=
NM_001382783.1:c.3204G=	NP_001369712.1:p.Leu1068=
NM_001382784.1:c.3411G=	NP_001369713.1:p.Leu1137=
NM_001382785.1:c.3396G=	NP_001369714.1:p.Leu1132=
NM_001382786.1:c.3375G=	NP_001369715.1:p.Leu1125=
NM_001382787.1:c.3369G=	NP_001369716.1:p.Leu1123=
NM_001382788.1:c.3324G=	NP_001369717.1:p.Leu1108=
NM_001382789.1:c.3315G=	NP_001369718.1:p.Leu1105=
NM_001382790.1:c.3291G=	NP_001369719.1:p.Leu1097=
NM_001382791.1:c.3285G=	NP_001369720.1:p.Leu1095=
NM_001382792.1:c.3258G=	NP_001369721.1:p.Leu1086=
NM_001382793.1:c.3252G=	NP_001369722.1:p.Leu1084=
NM_001382794.1:c.3252G=	NP_001369723.1:p.Leu1084=
NM_001382795.1:c.3246G=	NP_001369724.1:p.Leu1082=
NM_001382796.1:c.3207G=	NP_001369725.1:p.Leu1069=
NM_001382797.1:c.3195G=	NP_001369726.1:p.Leu1065=
NM_001382798.1:c.3138G=	NP_001369727.1:p.Leu1046=
NM_001382799.1:c.3114G=	NP_001369728.1:p.Leu1038=
NM_001382800.1:c.3108G=	NP_001369729.1:p.Leu1036=
NM_001382801.1:c.3090G=	NP_001369730.1:p.Leu1030=
NM_001382802.1:c.3036G=	NP_001369731.1:p.Leu1012=
NM_001382803.1:c.3118-260G=	NP_001369732.1:n.3118-260G=
NM_001382804.1:c.2466G=	NP_001369733.1:p.Leu822=
NM_001382805.1:c.2343G=	NP_001369734.1:p.Leu781=
NM_001382806.1:c.2256G=	NP_001369735.1:p.Leu752=
NM_004448.4:c.3294G= MANE Select	NP_004439.2:p.Leu1098=
NR_110535.2:n.3532G=