Canonical Allele Identifier: CA2259229283

Gene: ERBB2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727837_39727838delinsTG , CM000679.2:g.39727837_39727838delinsTG	GRCh38
NC_000017.10:g.37884090_37884091delinsTG , CM000679.1:g.37884090_37884091delinsTG	GRCh37
NC_000017.9:g.35137616_35137617delinsTG	NCBI36
NG_007503.1:g.44698_44699delinsTG , LRG_724:g.44698_44699delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3561_3562delinsTG MANE Select	ENSP00000269571.4:p.Phe1187=
ENST00000269571.9:c.3561_3562delinsTG	ENSP00000269571.4:p.Phe1187=
ENST00000406381.6:c.3471_3472delinsTG	ENSP00000385185.2:p.Phe1157=
ENST00000445658.6:c.2733_2734delinsTG	ENSP00000404047.2:p.Phe911=
ENST00000541774.5:c.3516_3517delinsTG	ENSP00000446466.1:p.Phe1172=
ENST00000578373.5:c.*3351_*3352delinsTG	ENSP00000463427.1:n.*3351_*3352delinsTG
ENST00000584450.5:c.*140_*141delinsTG	ENSP00000463714.1:n.*140_*141delinsTG
ENST00000584601.5:c.3471_3472delinsTG	ENSP00000462438.1:p.Phe1157=
NM_001005862.2:c.3471_3472delinsTG , LRG_724t1:c.3471_3472delinsTG	NP_001005862.1:p.Phe1157=
NM_001289936.1:c.3516_3517delinsTG , LRG_724t4:c.3516_3517delinsTG	NP_001276865.1:p.Phe1172=
NM_001289937.1:c.*140_*141delinsTG	NP_001276866.1:n.*140_*141delinsTG
NM_004448.3:c.3561_3562delinsTG , LRG_724t2:c.3561_3562delinsTG	NP_004439.2:p.Phe1187=
NR_110535.1:n.3885_3886delinsTG
XM_024450641.1:c.3699_3700delinsTG	XP_024306409.1:p.Phe1233=
XM_024450642.1:c.3654_3655delinsTG	XP_024306410.1:p.Phe1218=
XM_024450643.1:c.3609_3610delinsTG	XP_024306411.1:p.Phe1203=
NM_001005862.3:c.3471_3472delinsTG	NP_001005862.1:p.Phe1157=
NM_001289936.2:c.3516_3517delinsTG	NP_001276865.1:p.Phe1172=
NM_001289937.2:c.*140_*141delinsTG	NP_001276866.1:n.*140_*141delinsTG
NM_001382782.1:c.3471_3472delinsTG	NP_001369711.1:p.Phe1157=
NM_001382783.1:c.3471_3472delinsTG	NP_001369712.1:p.Phe1157=
NM_001382784.1:c.3678_3679delinsTG	NP_001369713.1:p.Phe1226=
NM_001382785.1:c.3663_3664delinsTG	NP_001369714.1:p.Phe1221=
NM_001382786.1:c.3642_3643delinsTG	NP_001369715.1:p.Phe1214=
NM_001382787.1:c.3636_3637delinsTG	NP_001369716.1:p.Phe1212=
NM_001382788.1:c.3591_3592delinsTG	NP_001369717.1:p.Phe1197=
NM_001382789.1:c.3582_3583delinsTG	NP_001369718.1:p.Phe1194=
NM_001382790.1:c.3558_3559delinsTG	NP_001369719.1:p.Phe1186=
NM_001382791.1:c.3552_3553delinsTG	NP_001369720.1:p.Phe1184=
NM_001382792.1:c.3525_3526delinsTG	NP_001369721.1:p.Phe1175=
NM_001382793.1:c.3519_3520delinsTG	NP_001369722.1:p.Phe1173=
NM_001382794.1:c.3519_3520delinsTG	NP_001369723.1:p.Phe1173=
NM_001382795.1:c.3513_3514delinsTG	NP_001369724.1:p.Phe1171=
NM_001382796.1:c.3474_3475delinsTG	NP_001369725.1:p.Phe1158=
NM_001382797.1:c.3462_3463delinsTG	NP_001369726.1:p.Phe1154=
NM_001382798.1:c.3405_3406delinsTG	NP_001369727.1:p.Phe1135=
NM_001382799.1:c.3381_3382delinsTG	NP_001369728.1:p.Phe1127=
NM_001382800.1:c.3375_3376delinsTG	NP_001369729.1:p.Phe1125=
NM_001382801.1:c.3357_3358delinsTG	NP_001369730.1:p.Phe1119=
NM_001382802.1:c.3303_3304delinsTG	NP_001369731.1:p.Phe1101=
NM_001382803.1:c.*140_*141delinsTG	NP_001369732.1:n.*140_*141delinsTG
NM_001382804.1:c.2733_2734delinsTG	NP_001369733.1:p.Phe911=
NM_001382805.1:c.2610_2611delinsTG	NP_001369734.1:p.Phe870=
NM_001382806.1:c.2523_2524delinsTG	NP_001369735.1:p.Phe841=
NM_004448.4:c.3561_3562delinsTG MANE Select	NP_004439.2:p.Phe1187=
NR_110535.2:n.3799_3800delinsTG