Canonical Allele Identifier: CA2259229146
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727530C= , CM000679.2:g.39727530C= GRCh38
NC_000017.10:g.37883783C= , CM000679.1:g.37883783C= GRCh37
NC_000017.9:g.35137309C= NCBI36
NG_007503.1:g.44391C= , LRG_724:g.44391C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3395C= MANE Select ENSP00000269571.4:p.Thr1132=
ENST00000269571.9:c.3395C= ENSP00000269571.4:p.Thr1132=
ENST00000406381.6:c.3305C= ENSP00000385185.2:p.Thr1102=
ENST00000445658.6:c.2567C= ENSP00000404047.2:p.Thr856=
ENST00000541774.5:c.3350C= ENSP00000446466.1:p.Thr1117=
ENST00000578373.5:c.*3185C= ENSP00000463427.1:n.*3185C=
ENST00000584450.5:c.3160-159C= ENSP00000463714.1:n.3160-159C=
ENST00000584601.5:c.3305C= ENSP00000462438.1:p.Thr1102=
NM_001005862.2:c.3305C= , LRG_724t1:c.3305C= NP_001005862.1:p.Thr1102=
NM_001289936.1:c.3350C= , LRG_724t4:c.3350C= NP_001276865.1:p.Thr1117=
NM_001289937.1:c.3160-159C= NP_001276866.1:n.3160-159C=
NM_004448.3:c.3395C= , LRG_724t2:c.3395C= NP_004439.2:p.Thr1132=
NR_110535.1:n.3719C=
XM_024450641.1:c.3533C= XP_024306409.1:p.Thr1178=
XM_024450642.1:c.3488C= XP_024306410.1:p.Thr1163=
XM_024450643.1:c.3443C= XP_024306411.1:p.Thr1148=
NM_001005862.3:c.3305C= NP_001005862.1:p.Thr1102=
NM_001289936.2:c.3350C= NP_001276865.1:p.Thr1117=
NM_001289937.2:c.3160-159C= NP_001276866.1:n.3160-159C=
NM_001382782.1:c.3305C= NP_001369711.1:p.Thr1102=
NM_001382783.1:c.3305C= NP_001369712.1:p.Thr1102=
NM_001382784.1:c.3512C= NP_001369713.1:p.Thr1171=
NM_001382785.1:c.3497C= NP_001369714.1:p.Thr1166=
NM_001382786.1:c.3476C= NP_001369715.1:p.Thr1159=
NM_001382787.1:c.3470C= NP_001369716.1:p.Thr1157=
NM_001382788.1:c.3425C= NP_001369717.1:p.Thr1142=
NM_001382789.1:c.3416C= NP_001369718.1:p.Thr1139=
NM_001382790.1:c.3392C= NP_001369719.1:p.Thr1131=
NM_001382791.1:c.3386C= NP_001369720.1:p.Thr1129=
NM_001382792.1:c.3359C= NP_001369721.1:p.Thr1120=
NM_001382793.1:c.3353C= NP_001369722.1:p.Thr1118=
NM_001382794.1:c.3353C= NP_001369723.1:p.Thr1118=
NM_001382795.1:c.3347C= NP_001369724.1:p.Thr1116=
NM_001382796.1:c.3308C= NP_001369725.1:p.Thr1103=
NM_001382797.1:c.3296C= NP_001369726.1:p.Thr1099=
NM_001382798.1:c.3239C= NP_001369727.1:p.Thr1080=
NM_001382799.1:c.3215C= NP_001369728.1:p.Thr1072=
NM_001382800.1:c.3209C= NP_001369729.1:p.Thr1070=
NM_001382801.1:c.3191C= NP_001369730.1:p.Thr1064=
NM_001382802.1:c.3137C= NP_001369731.1:p.Thr1046=
NM_001382803.1:c.3118-159C= NP_001369732.1:n.3118-159C=
NM_001382804.1:c.2567C= NP_001369733.1:p.Thr856=
NM_001382805.1:c.2444C= NP_001369734.1:p.Thr815=
NM_001382806.1:c.2357C= NP_001369735.1:p.Thr786=
NM_004448.4:c.3395C= MANE Select NP_004439.2:p.Thr1132=
NR_110535.2:n.3633C=