Canonical Allele Identifier: CA2259229149
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727537C= , CM000679.2:g.39727537C= GRCh38
NC_000017.10:g.37883790C= , CM000679.1:g.37883790C= GRCh37
NC_000017.9:g.35137316C= NCBI36
NG_007503.1:g.44398C= , LRG_724:g.44398C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3402C= MANE Select ENSP00000269571.4:p.Ser1134=
ENST00000269571.9:c.3402C= ENSP00000269571.4:p.Ser1134=
ENST00000406381.6:c.3312C= ENSP00000385185.2:p.Ser1104=
ENST00000445658.6:c.2574C= ENSP00000404047.2:p.Ser858=
ENST00000541774.5:c.3357C= ENSP00000446466.1:p.Ser1119=
ENST00000578373.5:c.*3192C= ENSP00000463427.1:n.*3192C=
ENST00000584450.5:c.3160-152C= ENSP00000463714.1:n.3160-152C=
ENST00000584601.5:c.3312C= ENSP00000462438.1:p.Ser1104=
NM_001005862.2:c.3312C= , LRG_724t1:c.3312C= NP_001005862.1:p.Ser1104=
NM_001289936.1:c.3357C= , LRG_724t4:c.3357C= NP_001276865.1:p.Ser1119=
NM_001289937.1:c.3160-152C= NP_001276866.1:n.3160-152C=
NM_004448.3:c.3402C= , LRG_724t2:c.3402C= NP_004439.2:p.Ser1134=
NR_110535.1:n.3726C=
XM_024450641.1:c.3540C= XP_024306409.1:p.Ser1180=
XM_024450642.1:c.3495C= XP_024306410.1:p.Ser1165=
XM_024450643.1:c.3450C= XP_024306411.1:p.Ser1150=
NM_001005862.3:c.3312C= NP_001005862.1:p.Ser1104=
NM_001289936.2:c.3357C= NP_001276865.1:p.Ser1119=
NM_001289937.2:c.3160-152C= NP_001276866.1:n.3160-152C=
NM_001382782.1:c.3312C= NP_001369711.1:p.Ser1104=
NM_001382783.1:c.3312C= NP_001369712.1:p.Ser1104=
NM_001382784.1:c.3519C= NP_001369713.1:p.Ser1173=
NM_001382785.1:c.3504C= NP_001369714.1:p.Ser1168=
NM_001382786.1:c.3483C= NP_001369715.1:p.Ser1161=
NM_001382787.1:c.3477C= NP_001369716.1:p.Ser1159=
NM_001382788.1:c.3432C= NP_001369717.1:p.Ser1144=
NM_001382789.1:c.3423C= NP_001369718.1:p.Ser1141=
NM_001382790.1:c.3399C= NP_001369719.1:p.Ser1133=
NM_001382791.1:c.3393C= NP_001369720.1:p.Ser1131=
NM_001382792.1:c.3366C= NP_001369721.1:p.Ser1122=
NM_001382793.1:c.3360C= NP_001369722.1:p.Ser1120=
NM_001382794.1:c.3360C= NP_001369723.1:p.Ser1120=
NM_001382795.1:c.3354C= NP_001369724.1:p.Ser1118=
NM_001382796.1:c.3315C= NP_001369725.1:p.Ser1105=
NM_001382797.1:c.3303C= NP_001369726.1:p.Ser1101=
NM_001382798.1:c.3246C= NP_001369727.1:p.Ser1082=
NM_001382799.1:c.3222C= NP_001369728.1:p.Ser1074=
NM_001382800.1:c.3216C= NP_001369729.1:p.Ser1072=
NM_001382801.1:c.3198C= NP_001369730.1:p.Ser1066=
NM_001382802.1:c.3144C= NP_001369731.1:p.Ser1048=
NM_001382803.1:c.3118-152C= NP_001369732.1:n.3118-152C=
NM_001382804.1:c.2574C= NP_001369733.1:p.Ser858=
NM_001382805.1:c.2451C= NP_001369734.1:p.Ser817=
NM_001382806.1:c.2364C= NP_001369735.1:p.Ser788=
NM_004448.4:c.3402C= MANE Select NP_004439.2:p.Ser1134=
NR_110535.2:n.3640C=