Canonical Allele Identifier: CA2259228758
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727388G= , CM000679.2:g.39727388G= GRCh38
NC_000017.10:g.37883641G= , CM000679.1:g.37883641G= GRCh37
NC_000017.9:g.35137167G= NCBI36
NG_007503.1:g.44249G= , LRG_724:g.44249G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3253G= MANE Select ENSP00000269571.4:p.Val1085=
ENST00000269571.9:c.3253G= ENSP00000269571.4:p.Val1085=
ENST00000406381.6:c.3163G= ENSP00000385185.2:p.Val1055=
ENST00000445658.6:c.2425G= ENSP00000404047.2:p.Val809=
ENST00000541774.5:c.3208G= ENSP00000446466.1:p.Val1070=
ENST00000578373.5:c.*3043G= ENSP00000463427.1:n.*3043G=
ENST00000584450.5:c.3160-301G= ENSP00000463714.1:n.3160-301G=
ENST00000584601.5:c.3163G= ENSP00000462438.1:p.Val1055=
NM_001005862.2:c.3163G= , LRG_724t1:c.3163G= NP_001005862.1:p.Val1055=
NM_001289936.1:c.3208G= , LRG_724t4:c.3208G= NP_001276865.1:p.Val1070=
NM_001289937.1:c.3160-301G= NP_001276866.1:n.3160-301G=
NM_004448.3:c.3253G= , LRG_724t2:c.3253G= NP_004439.2:p.Val1085=
NR_110535.1:n.3577G=
XM_024450641.1:c.3391G= XP_024306409.1:p.Val1131=
XM_024450642.1:c.3346G= XP_024306410.1:p.Val1116=
XM_024450643.1:c.3301G= XP_024306411.1:p.Val1101=
NM_001005862.3:c.3163G= NP_001005862.1:p.Val1055=
NM_001289936.2:c.3208G= NP_001276865.1:p.Val1070=
NM_001289937.2:c.3160-301G= NP_001276866.1:n.3160-301G=
NM_001382782.1:c.3163G= NP_001369711.1:p.Val1055=
NM_001382783.1:c.3163G= NP_001369712.1:p.Val1055=
NM_001382784.1:c.3370G= NP_001369713.1:p.Val1124=
NM_001382785.1:c.3355G= NP_001369714.1:p.Val1119=
NM_001382786.1:c.3334G= NP_001369715.1:p.Val1112=
NM_001382787.1:c.3328G= NP_001369716.1:p.Val1110=
NM_001382788.1:c.3283G= NP_001369717.1:p.Val1095=
NM_001382789.1:c.3274G= NP_001369718.1:p.Val1092=
NM_001382790.1:c.3250G= NP_001369719.1:p.Val1084=
NM_001382791.1:c.3244G= NP_001369720.1:p.Val1082=
NM_001382792.1:c.3217G= NP_001369721.1:p.Val1073=
NM_001382793.1:c.3211G= NP_001369722.1:p.Val1071=
NM_001382794.1:c.3211G= NP_001369723.1:p.Val1071=
NM_001382795.1:c.3205G= NP_001369724.1:p.Val1069=
NM_001382796.1:c.3166G= NP_001369725.1:p.Val1056=
NM_001382797.1:c.3154G= NP_001369726.1:p.Val1052=
NM_001382798.1:c.3097G= NP_001369727.1:p.Val1033=
NM_001382799.1:c.3073G= NP_001369728.1:p.Val1025=
NM_001382800.1:c.3067G= NP_001369729.1:p.Val1023=
NM_001382801.1:c.3049G= NP_001369730.1:p.Val1017=
NM_001382802.1:c.2995G= NP_001369731.1:p.Val999=
NM_001382803.1:c.3118-301G= NP_001369732.1:n.3118-301G=
NM_001382804.1:c.2425G= NP_001369733.1:p.Val809=
NM_001382805.1:c.2302G= NP_001369734.1:p.Val768=
NM_001382806.1:c.2215G= NP_001369735.1:p.Val739=
NM_004448.4:c.3253G= MANE Select NP_004439.2:p.Val1085=
NR_110535.2:n.3491G=