Canonical Allele Identifier: CA2637630595

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727848-TGGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727850_39727852del , CM000679.2:g.39727850_39727852del	GRCh38
NC_000017.10:g.37884103_37884105del , CM000679.1:g.37884103_37884105del	GRCh37
NC_000017.9:g.35137629_35137631del	NCBI36
NG_007503.1:g.44711_44713del , LRG_724:g.44711_44713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3574_3576del MANE Select	ENSP00000269571.4:p.Glu1192del
ENST00000269571.9:c.3574_3576del	ENSP00000269571.4:p.Glu1192del
ENST00000406381.6:c.3484_3486del	ENSP00000385185.2:p.Glu1162del
ENST00000445658.6:c.2746_2748del	ENSP00000404047.2:p.Glu916del
ENST00000541774.5:c.3529_3531del	ENSP00000446466.1:p.Glu1177del
ENST00000578373.5:c.*3364_*3366del	ENSP00000463427.1:n.*3364_*3366del
ENST00000584450.5:c.*153_*155del	ENSP00000463714.1:n.*153_*155del
ENST00000584601.5:c.3484_3486del	ENSP00000462438.1:p.Glu1162del
NM_001005862.2:c.3484_3486del , LRG_724t1:c.3484_3486del	NP_001005862.1:p.Glu1162del
NM_001289936.1:c.3529_3531del , LRG_724t4:c.3529_3531del	NP_001276865.1:p.Glu1177del
NM_001289937.1:c.*153_*155del	NP_001276866.1:n.*153_*155del
NM_004448.3:c.3574_3576del , LRG_724t2:c.3574_3576del	NP_004439.2:p.Glu1192del
NR_110535.1:n.3898_3900del
XM_024450641.1:c.3712_3714del	XP_024306409.1:p.Glu1238del
XM_024450642.1:c.3667_3669del	XP_024306410.1:p.Glu1223del
XM_024450643.1:c.3622_3624del	XP_024306411.1:p.Glu1208del
NM_001005862.3:c.3484_3486del	NP_001005862.1:p.Glu1162del
NM_001289936.2:c.3529_3531del	NP_001276865.1:p.Glu1177del
NM_001289937.2:c.*153_*155del	NP_001276866.1:n.*153_*155del
NM_001382782.1:c.3484_3486del	NP_001369711.1:p.Glu1162del
NM_001382783.1:c.3484_3486del	NP_001369712.1:p.Glu1162del
NM_001382784.1:c.3691_3693del	NP_001369713.1:p.Glu1231del
NM_001382785.1:c.3676_3678del	NP_001369714.1:p.Glu1226del
NM_001382786.1:c.3655_3657del	NP_001369715.1:p.Glu1219del
NM_001382787.1:c.3649_3651del	NP_001369716.1:p.Glu1217del
NM_001382788.1:c.3604_3606del	NP_001369717.1:p.Glu1202del
NM_001382789.1:c.3595_3597del	NP_001369718.1:p.Glu1199del
NM_001382790.1:c.3571_3573del	NP_001369719.1:p.Glu1191del
NM_001382791.1:c.3565_3567del	NP_001369720.1:p.Glu1189del
NM_001382792.1:c.3538_3540del	NP_001369721.1:p.Glu1180del
NM_001382793.1:c.3532_3534del	NP_001369722.1:p.Glu1178del
NM_001382794.1:c.3532_3534del	NP_001369723.1:p.Glu1178del
NM_001382795.1:c.3526_3528del	NP_001369724.1:p.Glu1176del
NM_001382796.1:c.3487_3489del	NP_001369725.1:p.Glu1163del
NM_001382797.1:c.3475_3477del	NP_001369726.1:p.Glu1159del
NM_001382798.1:c.3418_3420del	NP_001369727.1:p.Glu1140del
NM_001382799.1:c.3394_3396del	NP_001369728.1:p.Glu1132del
NM_001382800.1:c.3388_3390del	NP_001369729.1:p.Glu1130del
NM_001382801.1:c.3370_3372del	NP_001369730.1:p.Glu1124del
NM_001382802.1:c.3316_3318del	NP_001369731.1:p.Glu1106del
NM_001382803.1:c.*153_*155del	NP_001369732.1:n.*153_*155del
NM_001382804.1:c.2746_2748del	NP_001369733.1:p.Glu916del
NM_001382805.1:c.2623_2625del	NP_001369734.1:p.Glu875del
NM_001382806.1:c.2536_2538del	NP_001369735.1:p.Glu846del
NM_004448.4:c.3574_3576del MANE Select	NP_004439.2:p.Glu1192del
NR_110535.2:n.3812_3814del