Canonical Allele Identifier: CA2637630795

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727887-C-CCCCTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727888_39727893dup , CM000679.2:g.39727888_39727893dup	GRCh38
NC_000017.10:g.37884141_37884146dup , CM000679.1:g.37884141_37884146dup	GRCh37
NC_000017.9:g.35137667_35137672dup	NCBI36
NG_007503.1:g.44749_44754dup , LRG_724:g.44749_44754dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3612_3617dup MANE Select	ENSP00000269571.4:p.Pro1205_Gln1206insHisPro
ENST00000269571.9:c.3612_3617dup	ENSP00000269571.4:p.Pro1205_Gln1206insHisPro
ENST00000406381.6:c.3522_3527dup	ENSP00000385185.2:p.Pro1175_Gln1176insHisPro
ENST00000445658.6:c.2784_2789dup	ENSP00000404047.2:p.Pro929_Gln930insHisPro
ENST00000541774.5:c.3567_3572dup	ENSP00000446466.1:p.Pro1190_Gln1191insHisPro
ENST00000578373.5:c.*3402_*3407dup	ENSP00000463427.1:n.*3402_*3407dup
ENST00000584450.5:c.*191_*196dup	ENSP00000463714.1:n.*191_*196dup
ENST00000584601.5:c.3522_3527dup	ENSP00000462438.1:p.Pro1175_Gln1176insHisPro
NM_001005862.2:c.3522_3527dup , LRG_724t1:c.3522_3527dup	NP_001005862.1:p.Pro1175_Gln1176insHisPro
NM_001289936.1:c.3567_3572dup , LRG_724t4:c.3567_3572dup	NP_001276865.1:p.Pro1190_Gln1191insHisPro
NM_001289937.1:c.*191_*196dup	NP_001276866.1:n.*191_*196dup
NM_004448.3:c.3612_3617dup , LRG_724t2:c.3612_3617dup	NP_004439.2:p.Pro1205_Gln1206insHisPro
NR_110535.1:n.3936_3941dup
XM_024450641.1:c.3750_3755dup	XP_024306409.1:p.Pro1251_Gln1252insHisPro
XM_024450642.1:c.3705_3710dup	XP_024306410.1:p.Pro1236_Gln1237insHisPro
XM_024450643.1:c.3660_3665dup	XP_024306411.1:p.Pro1221_Gln1222insHisPro
NM_001005862.3:c.3522_3527dup	NP_001005862.1:p.Pro1175_Gln1176insHisPro
NM_001289936.2:c.3567_3572dup	NP_001276865.1:p.Pro1190_Gln1191insHisPro
NM_001289937.2:c.*191_*196dup	NP_001276866.1:n.*191_*196dup
NM_001382782.1:c.3522_3527dup	NP_001369711.1:p.Pro1175_Gln1176insHisPro
NM_001382783.1:c.3522_3527dup	NP_001369712.1:p.Pro1175_Gln1176insHisPro
NM_001382784.1:c.3729_3734dup	NP_001369713.1:p.Pro1244_Gln1245insHisPro
NM_001382785.1:c.3714_3719dup	NP_001369714.1:p.Pro1239_Gln1240insHisPro
NM_001382786.1:c.3693_3698dup	NP_001369715.1:p.Pro1232_Gln1233insHisPro
NM_001382787.1:c.3687_3692dup	NP_001369716.1:p.Pro1230_Gln1231insHisPro
NM_001382788.1:c.3642_3647dup	NP_001369717.1:p.Pro1215_Gln1216insHisPro
NM_001382789.1:c.3633_3638dup	NP_001369718.1:p.Pro1212_Gln1213insHisPro
NM_001382790.1:c.3609_3614dup	NP_001369719.1:p.Pro1204_Gln1205insHisPro
NM_001382791.1:c.3603_3608dup	NP_001369720.1:p.Pro1202_Gln1203insHisPro
NM_001382792.1:c.3576_3581dup	NP_001369721.1:p.Pro1193_Gln1194insHisPro
NM_001382793.1:c.3570_3575dup	NP_001369722.1:p.Pro1191_Gln1192insHisPro
NM_001382794.1:c.3570_3575dup	NP_001369723.1:p.Pro1191_Gln1192insHisPro
NM_001382795.1:c.3564_3569dup	NP_001369724.1:p.Pro1189_Gln1190insHisPro
NM_001382796.1:c.3525_3530dup	NP_001369725.1:p.Pro1176_Gln1177insHisPro
NM_001382797.1:c.3513_3518dup	NP_001369726.1:p.Pro1172_Gln1173insHisPro
NM_001382798.1:c.3456_3461dup	NP_001369727.1:p.Pro1153_Gln1154insHisPro
NM_001382799.1:c.3432_3437dup	NP_001369728.1:p.Pro1145_Gln1146insHisPro
NM_001382800.1:c.3426_3431dup	NP_001369729.1:p.Pro1143_Gln1144insHisPro
NM_001382801.1:c.3408_3413dup	NP_001369730.1:p.Pro1137_Gln1138insHisPro
NM_001382802.1:c.3354_3359dup	NP_001369731.1:p.Pro1119_Gln1120insHisPro
NM_001382803.1:c.*191_*196dup	NP_001369732.1:n.*191_*196dup
NM_001382804.1:c.2784_2789dup	NP_001369733.1:p.Pro929_Gln930insHisPro
NM_001382805.1:c.2661_2666dup	NP_001369734.1:p.Pro888_Gln889insHisPro
NM_001382806.1:c.2574_2579dup	NP_001369735.1:p.Pro859_Gln860insHisPro
NM_004448.4:c.3612_3617dup MANE Select	NP_004439.2:p.Pro1205_Gln1206insHisPro
NR_110535.2:n.3850_3855dup