Canonical Allele Identifier: CA2259229221
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727699C= , CM000679.2:g.39727699C= GRCh38
NC_000017.10:g.37883952C= , CM000679.1:g.37883952C= GRCh37
NC_000017.9:g.35137478C= NCBI36
NG_007503.1:g.44560C= , LRG_724:g.44560C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3423C= MANE Select ENSP00000269571.4:p.Asn1141=
ENST00000269571.9:c.3423C= ENSP00000269571.4:p.Asn1141=
ENST00000406381.6:c.3333C= ENSP00000385185.2:p.Asn1111=
ENST00000445658.6:c.2595C= ENSP00000404047.2:p.Asn865=
ENST00000541774.5:c.3378C= ENSP00000446466.1:p.Asn1126=
ENST00000578373.5:c.*3213C= ENSP00000463427.1:n.*3213C=
ENST00000584450.5:c.*2C= ENSP00000463714.1:n.*2C=
ENST00000584601.5:c.3333C= ENSP00000462438.1:p.Asn1111=
NM_001005862.2:c.3333C= , LRG_724t1:c.3333C= NP_001005862.1:p.Asn1111=
NM_001289936.1:c.3378C= , LRG_724t4:c.3378C= NP_001276865.1:p.Asn1126=
NM_001289937.1:c.*2C= NP_001276866.1:n.*2C=
NM_004448.3:c.3423C= , LRG_724t2:c.3423C= NP_004439.2:p.Asn1141=
NR_110535.1:n.3747C=
XM_024450641.1:c.3561C= XP_024306409.1:p.Asn1187=
XM_024450642.1:c.3516C= XP_024306410.1:p.Asn1172=
XM_024450643.1:c.3471C= XP_024306411.1:p.Asn1157=
NM_001005862.3:c.3333C= NP_001005862.1:p.Asn1111=
NM_001289936.2:c.3378C= NP_001276865.1:p.Asn1126=
NM_001289937.2:c.*2C= NP_001276866.1:n.*2C=
NM_001382782.1:c.3333C= NP_001369711.1:p.Asn1111=
NM_001382783.1:c.3333C= NP_001369712.1:p.Asn1111=
NM_001382784.1:c.3540C= NP_001369713.1:p.Asn1180=
NM_001382785.1:c.3525C= NP_001369714.1:p.Asn1175=
NM_001382786.1:c.3504C= NP_001369715.1:p.Asn1168=
NM_001382787.1:c.3498C= NP_001369716.1:p.Asn1166=
NM_001382788.1:c.3453C= NP_001369717.1:p.Asn1151=
NM_001382789.1:c.3444C= NP_001369718.1:p.Asn1148=
NM_001382790.1:c.3420C= NP_001369719.1:p.Asn1140=
NM_001382791.1:c.3414C= NP_001369720.1:p.Asn1138=
NM_001382792.1:c.3387C= NP_001369721.1:p.Asn1129=
NM_001382793.1:c.3381C= NP_001369722.1:p.Asn1127=
NM_001382794.1:c.3381C= NP_001369723.1:p.Asn1127=
NM_001382795.1:c.3375C= NP_001369724.1:p.Asn1125=
NM_001382796.1:c.3336C= NP_001369725.1:p.Asn1112=
NM_001382797.1:c.3324C= NP_001369726.1:p.Asn1108=
NM_001382798.1:c.3267C= NP_001369727.1:p.Asn1089=
NM_001382799.1:c.3243C= NP_001369728.1:p.Asn1081=
NM_001382800.1:c.3237C= NP_001369729.1:p.Asn1079=
NM_001382801.1:c.3219C= NP_001369730.1:p.Asn1073=
NM_001382802.1:c.3165C= NP_001369731.1:p.Asn1055=
NM_001382803.1:c.*2C= NP_001369732.1:n.*2C=
NM_001382804.1:c.2595C= NP_001369733.1:p.Asn865=
NM_001382805.1:c.2472C= NP_001369734.1:p.Asn824=
NM_001382806.1:c.2385C= NP_001369735.1:p.Asn795=
NM_004448.4:c.3423C= MANE Select NP_004439.2:p.Asn1141=
NR_110535.2:n.3661C=