Canonical Allele Identifier: CA2259228818
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727456C= , CM000679.2:g.39727456C= GRCh38
NC_000017.10:g.37883709C= , CM000679.1:g.37883709C= GRCh37
NC_000017.9:g.35137235C= NCBI36
NG_007503.1:g.44317C= , LRG_724:g.44317C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3321C= MANE Select ENSP00000269571.4:p.Ser1107=
ENST00000269571.9:c.3321C= ENSP00000269571.4:p.Ser1107=
ENST00000406381.6:c.3231C= ENSP00000385185.2:p.Ser1077=
ENST00000445658.6:c.2493C= ENSP00000404047.2:p.Ser831=
ENST00000541774.5:c.3276C= ENSP00000446466.1:p.Ser1092=
ENST00000578373.5:c.*3111C= ENSP00000463427.1:n.*3111C=
ENST00000584450.5:c.3160-233C= ENSP00000463714.1:n.3160-233C=
ENST00000584601.5:c.3231C= ENSP00000462438.1:p.Ser1077=
NM_001005862.2:c.3231C= , LRG_724t1:c.3231C= NP_001005862.1:p.Ser1077=
NM_001289936.1:c.3276C= , LRG_724t4:c.3276C= NP_001276865.1:p.Ser1092=
NM_001289937.1:c.3160-233C= NP_001276866.1:n.3160-233C=
NM_004448.3:c.3321C= , LRG_724t2:c.3321C= NP_004439.2:p.Ser1107=
NR_110535.1:n.3645C=
XM_024450641.1:c.3459C= XP_024306409.1:p.Ser1153=
XM_024450642.1:c.3414C= XP_024306410.1:p.Ser1138=
XM_024450643.1:c.3369C= XP_024306411.1:p.Ser1123=
NM_001005862.3:c.3231C= NP_001005862.1:p.Ser1077=
NM_001289936.2:c.3276C= NP_001276865.1:p.Ser1092=
NM_001289937.2:c.3160-233C= NP_001276866.1:n.3160-233C=
NM_001382782.1:c.3231C= NP_001369711.1:p.Ser1077=
NM_001382783.1:c.3231C= NP_001369712.1:p.Ser1077=
NM_001382784.1:c.3438C= NP_001369713.1:p.Ser1146=
NM_001382785.1:c.3423C= NP_001369714.1:p.Ser1141=
NM_001382786.1:c.3402C= NP_001369715.1:p.Ser1134=
NM_001382787.1:c.3396C= NP_001369716.1:p.Ser1132=
NM_001382788.1:c.3351C= NP_001369717.1:p.Ser1117=
NM_001382789.1:c.3342C= NP_001369718.1:p.Ser1114=
NM_001382790.1:c.3318C= NP_001369719.1:p.Ser1106=
NM_001382791.1:c.3312C= NP_001369720.1:p.Ser1104=
NM_001382792.1:c.3285C= NP_001369721.1:p.Ser1095=
NM_001382793.1:c.3279C= NP_001369722.1:p.Ser1093=
NM_001382794.1:c.3279C= NP_001369723.1:p.Ser1093=
NM_001382795.1:c.3273C= NP_001369724.1:p.Ser1091=
NM_001382796.1:c.3234C= NP_001369725.1:p.Ser1078=
NM_001382797.1:c.3222C= NP_001369726.1:p.Ser1074=
NM_001382798.1:c.3165C= NP_001369727.1:p.Ser1055=
NM_001382799.1:c.3141C= NP_001369728.1:p.Ser1047=
NM_001382800.1:c.3135C= NP_001369729.1:p.Ser1045=
NM_001382801.1:c.3117C= NP_001369730.1:p.Ser1039=
NM_001382802.1:c.3063C= NP_001369731.1:p.Ser1021=
NM_001382803.1:c.3118-233C= NP_001369732.1:n.3118-233C=
NM_001382804.1:c.2493C= NP_001369733.1:p.Ser831=
NM_001382805.1:c.2370C= NP_001369734.1:p.Ser790=
NM_001382806.1:c.2283C= NP_001369735.1:p.Ser761=
NM_004448.4:c.3321C= MANE Select NP_004439.2:p.Ser1107=
NR_110535.2:n.3559C=