Canonical Allele Identifier: CA2637630913

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727900-CCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727907_39727909del , CM000679.2:g.39727907_39727909del	GRCh38
NC_000017.10:g.37884160_37884162del , CM000679.1:g.37884160_37884162del	GRCh37
NC_000017.9:g.35137686_35137688del	NCBI36
NG_007503.1:g.44768_44770del , LRG_724:g.44768_44770del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3631_3633del MANE Select	ENSP00000269571.4:p.Pro1211del
ENST00000269571.9:c.3631_3633del	ENSP00000269571.4:p.Pro1211del
ENST00000406381.6:c.3541_3543del	ENSP00000385185.2:p.Pro1181del
ENST00000445658.6:c.2803_2805del	ENSP00000404047.2:p.Pro935del
ENST00000541774.5:c.3586_3588del	ENSP00000446466.1:p.Pro1196del
ENST00000578373.5:c.*3421_*3423del	ENSP00000463427.1:n.*3421_*3423del
ENST00000584450.5:c.*210_*212del	ENSP00000463714.1:n.*210_*212del
ENST00000584601.5:c.3541_3543del	ENSP00000462438.1:p.Pro1181del
NM_001005862.2:c.3541_3543del , LRG_724t1:c.3541_3543del	NP_001005862.1:p.Pro1181del
NM_001289936.1:c.3586_3588del , LRG_724t4:c.3586_3588del	NP_001276865.1:p.Pro1196del
NM_001289937.1:c.*210_*212del	NP_001276866.1:n.*210_*212del
NM_004448.3:c.3631_3633del , LRG_724t2:c.3631_3633del	NP_004439.2:p.Pro1211del
NR_110535.1:n.3955_3957del
XM_024450641.1:c.3769_3771del	XP_024306409.1:p.Pro1257del
XM_024450642.1:c.3724_3726del	XP_024306410.1:p.Pro1242del
XM_024450643.1:c.3679_3681del	XP_024306411.1:p.Pro1227del
NM_001005862.3:c.3541_3543del	NP_001005862.1:p.Pro1181del
NM_001289936.2:c.3586_3588del	NP_001276865.1:p.Pro1196del
NM_001289937.2:c.*210_*212del	NP_001276866.1:n.*210_*212del
NM_001382782.1:c.3541_3543del	NP_001369711.1:p.Pro1181del
NM_001382783.1:c.3541_3543del	NP_001369712.1:p.Pro1181del
NM_001382784.1:c.3748_3750del	NP_001369713.1:p.Pro1250del
NM_001382785.1:c.3733_3735del	NP_001369714.1:p.Pro1245del
NM_001382786.1:c.3712_3714del	NP_001369715.1:p.Pro1238del
NM_001382787.1:c.3706_3708del	NP_001369716.1:p.Pro1236del
NM_001382788.1:c.3661_3663del	NP_001369717.1:p.Pro1221del
NM_001382789.1:c.3652_3654del	NP_001369718.1:p.Pro1218del
NM_001382790.1:c.3628_3630del	NP_001369719.1:p.Pro1210del
NM_001382791.1:c.3622_3624del	NP_001369720.1:p.Pro1208del
NM_001382792.1:c.3595_3597del	NP_001369721.1:p.Pro1199del
NM_001382793.1:c.3589_3591del	NP_001369722.1:p.Pro1197del
NM_001382794.1:c.3589_3591del	NP_001369723.1:p.Pro1197del
NM_001382795.1:c.3583_3585del	NP_001369724.1:p.Pro1195del
NM_001382796.1:c.3544_3546del	NP_001369725.1:p.Pro1182del
NM_001382797.1:c.3532_3534del	NP_001369726.1:p.Pro1178del
NM_001382798.1:c.3475_3477del	NP_001369727.1:p.Pro1159del
NM_001382799.1:c.3451_3453del	NP_001369728.1:p.Pro1151del
NM_001382800.1:c.3445_3447del	NP_001369729.1:p.Pro1149del
NM_001382801.1:c.3427_3429del	NP_001369730.1:p.Pro1143del
NM_001382802.1:c.3373_3375del	NP_001369731.1:p.Pro1125del
NM_001382803.1:c.*210_*212del	NP_001369732.1:n.*210_*212del
NM_001382804.1:c.2803_2805del	NP_001369733.1:p.Pro935del
NM_001382805.1:c.2680_2682del	NP_001369734.1:p.Pro894del
NM_001382806.1:c.2593_2595del	NP_001369735.1:p.Pro865del
NM_004448.4:c.3631_3633del MANE Select	NP_004439.2:p.Pro1211del
NR_110535.2:n.3869_3871del