Canonical Allele Identifier: CA2259229148
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727535A= , CM000679.2:g.39727535A= GRCh38
NC_000017.10:g.37883788A= , CM000679.1:g.37883788A= GRCh37
NC_000017.9:g.35137314A= NCBI36
NG_007503.1:g.44396A= , LRG_724:g.44396A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3400A= MANE Select ENSP00000269571.4:p.Ser1134=
ENST00000269571.9:c.3400A= ENSP00000269571.4:p.Ser1134=
ENST00000406381.6:c.3310A= ENSP00000385185.2:p.Ser1104=
ENST00000445658.6:c.2572A= ENSP00000404047.2:p.Ser858=
ENST00000541774.5:c.3355A= ENSP00000446466.1:p.Ser1119=
ENST00000578373.5:c.*3190A= ENSP00000463427.1:n.*3190A=
ENST00000584450.5:c.3160-154A= ENSP00000463714.1:n.3160-154A=
ENST00000584601.5:c.3310A= ENSP00000462438.1:p.Ser1104=
NM_001005862.2:c.3310A= , LRG_724t1:c.3310A= NP_001005862.1:p.Ser1104=
NM_001289936.1:c.3355A= , LRG_724t4:c.3355A= NP_001276865.1:p.Ser1119=
NM_001289937.1:c.3160-154A= NP_001276866.1:n.3160-154A=
NM_004448.3:c.3400A= , LRG_724t2:c.3400A= NP_004439.2:p.Ser1134=
NR_110535.1:n.3724A=
XM_024450641.1:c.3538A= XP_024306409.1:p.Ser1180=
XM_024450642.1:c.3493A= XP_024306410.1:p.Ser1165=
XM_024450643.1:c.3448A= XP_024306411.1:p.Ser1150=
NM_001005862.3:c.3310A= NP_001005862.1:p.Ser1104=
NM_001289936.2:c.3355A= NP_001276865.1:p.Ser1119=
NM_001289937.2:c.3160-154A= NP_001276866.1:n.3160-154A=
NM_001382782.1:c.3310A= NP_001369711.1:p.Ser1104=
NM_001382783.1:c.3310A= NP_001369712.1:p.Ser1104=
NM_001382784.1:c.3517A= NP_001369713.1:p.Ser1173=
NM_001382785.1:c.3502A= NP_001369714.1:p.Ser1168=
NM_001382786.1:c.3481A= NP_001369715.1:p.Ser1161=
NM_001382787.1:c.3475A= NP_001369716.1:p.Ser1159=
NM_001382788.1:c.3430A= NP_001369717.1:p.Ser1144=
NM_001382789.1:c.3421A= NP_001369718.1:p.Ser1141=
NM_001382790.1:c.3397A= NP_001369719.1:p.Ser1133=
NM_001382791.1:c.3391A= NP_001369720.1:p.Ser1131=
NM_001382792.1:c.3364A= NP_001369721.1:p.Ser1122=
NM_001382793.1:c.3358A= NP_001369722.1:p.Ser1120=
NM_001382794.1:c.3358A= NP_001369723.1:p.Ser1120=
NM_001382795.1:c.3352A= NP_001369724.1:p.Ser1118=
NM_001382796.1:c.3313A= NP_001369725.1:p.Ser1105=
NM_001382797.1:c.3301A= NP_001369726.1:p.Ser1101=
NM_001382798.1:c.3244A= NP_001369727.1:p.Ser1082=
NM_001382799.1:c.3220A= NP_001369728.1:p.Ser1074=
NM_001382800.1:c.3214A= NP_001369729.1:p.Ser1072=
NM_001382801.1:c.3196A= NP_001369730.1:p.Ser1066=
NM_001382802.1:c.3142A= NP_001369731.1:p.Ser1048=
NM_001382803.1:c.3118-154A= NP_001369732.1:n.3118-154A=
NM_001382804.1:c.2572A= NP_001369733.1:p.Ser858=
NM_001382805.1:c.2449A= NP_001369734.1:p.Ser817=
NM_001382806.1:c.2362A= NP_001369735.1:p.Ser788=
NM_004448.4:c.3400A= MANE Select NP_004439.2:p.Ser1134=
NR_110535.2:n.3638A=