Canonical Allele Identifier: CA2259228750
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727385G= , CM000679.2:g.39727385G= GRCh38
NC_000017.10:g.37883638G= , CM000679.1:g.37883638G= GRCh37
NC_000017.9:g.35137164G= NCBI36
NG_007503.1:g.44246G= , LRG_724:g.44246G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3250G= MANE Select ENSP00000269571.4:p.Asp1084=
ENST00000269571.9:c.3250G= ENSP00000269571.4:p.Asp1084=
ENST00000406381.6:c.3160G= ENSP00000385185.2:p.Asp1054=
ENST00000445658.6:c.2422G= ENSP00000404047.2:p.Asp808=
ENST00000541774.5:c.3205G= ENSP00000446466.1:p.Asp1069=
ENST00000578373.5:c.*3040G= ENSP00000463427.1:n.*3040G=
ENST00000584450.5:c.3160-304G= ENSP00000463714.1:n.3160-304G=
ENST00000584601.5:c.3160G= ENSP00000462438.1:p.Asp1054=
NM_001005862.2:c.3160G= , LRG_724t1:c.3160G= NP_001005862.1:p.Asp1054=
NM_001289936.1:c.3205G= , LRG_724t4:c.3205G= NP_001276865.1:p.Asp1069=
NM_001289937.1:c.3160-304G= NP_001276866.1:n.3160-304G=
NM_004448.3:c.3250G= , LRG_724t2:c.3250G= NP_004439.2:p.Asp1084=
NR_110535.1:n.3574G=
XM_024450641.1:c.3388G= XP_024306409.1:p.Asp1130=
XM_024450642.1:c.3343G= XP_024306410.1:p.Asp1115=
XM_024450643.1:c.3298G= XP_024306411.1:p.Asp1100=
NM_001005862.3:c.3160G= NP_001005862.1:p.Asp1054=
NM_001289936.2:c.3205G= NP_001276865.1:p.Asp1069=
NM_001289937.2:c.3160-304G= NP_001276866.1:n.3160-304G=
NM_001382782.1:c.3160G= NP_001369711.1:p.Asp1054=
NM_001382783.1:c.3160G= NP_001369712.1:p.Asp1054=
NM_001382784.1:c.3367G= NP_001369713.1:p.Asp1123=
NM_001382785.1:c.3352G= NP_001369714.1:p.Asp1118=
NM_001382786.1:c.3331G= NP_001369715.1:p.Asp1111=
NM_001382787.1:c.3325G= NP_001369716.1:p.Asp1109=
NM_001382788.1:c.3280G= NP_001369717.1:p.Asp1094=
NM_001382789.1:c.3271G= NP_001369718.1:p.Asp1091=
NM_001382790.1:c.3247G= NP_001369719.1:p.Asp1083=
NM_001382791.1:c.3241G= NP_001369720.1:p.Asp1081=
NM_001382792.1:c.3214G= NP_001369721.1:p.Asp1072=
NM_001382793.1:c.3208G= NP_001369722.1:p.Asp1070=
NM_001382794.1:c.3208G= NP_001369723.1:p.Asp1070=
NM_001382795.1:c.3202G= NP_001369724.1:p.Asp1068=
NM_001382796.1:c.3163G= NP_001369725.1:p.Asp1055=
NM_001382797.1:c.3151G= NP_001369726.1:p.Asp1051=
NM_001382798.1:c.3094G= NP_001369727.1:p.Asp1032=
NM_001382799.1:c.3070G= NP_001369728.1:p.Asp1024=
NM_001382800.1:c.3064G= NP_001369729.1:p.Asp1022=
NM_001382801.1:c.3046G= NP_001369730.1:p.Asp1016=
NM_001382802.1:c.2992G= NP_001369731.1:p.Asp998=
NM_001382803.1:c.3118-304G= NP_001369732.1:n.3118-304G=
NM_001382804.1:c.2422G= NP_001369733.1:p.Asp808=
NM_001382805.1:c.2299G= NP_001369734.1:p.Asp767=
NM_001382806.1:c.2212G= NP_001369735.1:p.Asp738=
NM_004448.4:c.3250G= MANE Select NP_004439.2:p.Asp1084=
NR_110535.2:n.3488G=