Canonical Allele Identifier: CA2259229305

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727889C= , CM000679.2:g.39727889C=	GRCh38
NC_000017.10:g.37884142C= , CM000679.1:g.37884142C=	GRCh37
NC_000017.9:g.35137668C=	NCBI36
NG_007503.1:g.44750C= , LRG_724:g.44750C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3613C= MANE Select	ENSP00000269571.4:p.Pro1205=
ENST00000269571.9:c.3613C=	ENSP00000269571.4:p.Pro1205=
ENST00000406381.6:c.3523C=	ENSP00000385185.2:p.Pro1175=
ENST00000445658.6:c.2785C=	ENSP00000404047.2:p.Pro929=
ENST00000541774.5:c.3568C=	ENSP00000446466.1:p.Pro1190=
ENST00000578373.5:c.*3403C=	ENSP00000463427.1:n.*3403C=
ENST00000584450.5:c.*192C=	ENSP00000463714.1:n.*192C=
ENST00000584601.5:c.3523C=	ENSP00000462438.1:p.Pro1175=
NM_001005862.2:c.3523C= , LRG_724t1:c.3523C=	NP_001005862.1:p.Pro1175=
NM_001289936.1:c.3568C= , LRG_724t4:c.3568C=	NP_001276865.1:p.Pro1190=
NM_001289937.1:c.*192C=	NP_001276866.1:n.*192C=
NM_004448.3:c.3613C= , LRG_724t2:c.3613C=	NP_004439.2:p.Pro1205=
NR_110535.1:n.3937C=
XM_024450641.1:c.3751C=	XP_024306409.1:p.Pro1251=
XM_024450642.1:c.3706C=	XP_024306410.1:p.Pro1236=
XM_024450643.1:c.3661C=	XP_024306411.1:p.Pro1221=
NM_001005862.3:c.3523C=	NP_001005862.1:p.Pro1175=
NM_001289936.2:c.3568C=	NP_001276865.1:p.Pro1190=
NM_001289937.2:c.*192C=	NP_001276866.1:n.*192C=
NM_001382782.1:c.3523C=	NP_001369711.1:p.Pro1175=
NM_001382783.1:c.3523C=	NP_001369712.1:p.Pro1175=
NM_001382784.1:c.3730C=	NP_001369713.1:p.Pro1244=
NM_001382785.1:c.3715C=	NP_001369714.1:p.Pro1239=
NM_001382786.1:c.3694C=	NP_001369715.1:p.Pro1232=
NM_001382787.1:c.3688C=	NP_001369716.1:p.Pro1230=
NM_001382788.1:c.3643C=	NP_001369717.1:p.Pro1215=
NM_001382789.1:c.3634C=	NP_001369718.1:p.Pro1212=
NM_001382790.1:c.3610C=	NP_001369719.1:p.Pro1204=
NM_001382791.1:c.3604C=	NP_001369720.1:p.Pro1202=
NM_001382792.1:c.3577C=	NP_001369721.1:p.Pro1193=
NM_001382793.1:c.3571C=	NP_001369722.1:p.Pro1191=
NM_001382794.1:c.3571C=	NP_001369723.1:p.Pro1191=
NM_001382795.1:c.3565C=	NP_001369724.1:p.Pro1189=
NM_001382796.1:c.3526C=	NP_001369725.1:p.Pro1176=
NM_001382797.1:c.3514C=	NP_001369726.1:p.Pro1172=
NM_001382798.1:c.3457C=	NP_001369727.1:p.Pro1153=
NM_001382799.1:c.3433C=	NP_001369728.1:p.Pro1145=
NM_001382800.1:c.3427C=	NP_001369729.1:p.Pro1143=
NM_001382801.1:c.3409C=	NP_001369730.1:p.Pro1137=
NM_001382802.1:c.3355C=	NP_001369731.1:p.Pro1119=
NM_001382803.1:c.*192C=	NP_001369732.1:n.*192C=
NM_001382804.1:c.2785C=	NP_001369733.1:p.Pro929=
NM_001382805.1:c.2662C=	NP_001369734.1:p.Pro888=
NM_001382806.1:c.2575C=	NP_001369735.1:p.Pro859=
NM_004448.4:c.3613C= MANE Select	NP_004439.2:p.Pro1205=
NR_110535.2:n.3851C=