Canonical Allele Identifier: CA771864457

Gene: ERBB2

Linked Data

• dbSNP Id: rs1240721363
• gnomAD v3: 17-39727876-GGGA-G
• gnomAD v4: 17-39727876-GGGA-G
• MyVariant Identifiers: chr17:g.37884130_37884132del (hg19) ; chr17:g.39727877_39727879del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727881_39727883del , CM000679.2:g.39727881_39727883del	GRCh38
NC_000017.10:g.37884134_37884136del , CM000679.1:g.37884134_37884136del	GRCh37
NC_000017.9:g.35137660_35137662del	NCBI36
NG_007503.1:g.44742_44744del , LRG_724:g.44742_44744del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3605_3607del MANE Select	ENSP00000269571.4:p.Gly1202del
ENST00000269571.9:c.3605_3607del	ENSP00000269571.4:p.Gly1202del
ENST00000406381.6:c.3515_3517del	ENSP00000385185.2:p.Gly1172del
ENST00000445658.6:c.2777_2779del	ENSP00000404047.2:p.Gly926del
ENST00000541774.5:c.3560_3562del	ENSP00000446466.1:p.Gly1187del
ENST00000578373.5:c.*3395_*3397del	ENSP00000463427.1:n.*3395_*3397del
ENST00000584450.5:c.*184_*186del	ENSP00000463714.1:n.*184_*186del
ENST00000584601.5:c.3515_3517del	ENSP00000462438.1:p.Gly1172del
NM_001005862.2:c.3515_3517del , LRG_724t1:c.3515_3517del	NP_001005862.1:p.Gly1172del
NM_001289936.1:c.3560_3562del , LRG_724t4:c.3560_3562del	NP_001276865.1:p.Gly1187del
NM_001289937.1:c.*184_*186del	NP_001276866.1:n.*184_*186del
NM_004448.3:c.3605_3607del , LRG_724t2:c.3605_3607del	NP_004439.2:p.Gly1202del
NR_110535.1:n.3929_3931del
XM_024450641.1:c.3743_3745del	XP_024306409.1:p.Gly1248del
XM_024450642.1:c.3698_3700del	XP_024306410.1:p.Gly1233del
XM_024450643.1:c.3653_3655del	XP_024306411.1:p.Gly1218del
NM_001005862.3:c.3515_3517del	NP_001005862.1:p.Gly1172del
NM_001289936.2:c.3560_3562del	NP_001276865.1:p.Gly1187del
NM_001289937.2:c.*184_*186del	NP_001276866.1:n.*184_*186del
NM_001382782.1:c.3515_3517del	NP_001369711.1:p.Gly1172del
NM_001382783.1:c.3515_3517del	NP_001369712.1:p.Gly1172del
NM_001382784.1:c.3722_3724del	NP_001369713.1:p.Gly1241del
NM_001382785.1:c.3707_3709del	NP_001369714.1:p.Gly1236del
NM_001382786.1:c.3686_3688del	NP_001369715.1:p.Gly1229del
NM_001382787.1:c.3680_3682del	NP_001369716.1:p.Gly1227del
NM_001382788.1:c.3635_3637del	NP_001369717.1:p.Gly1212del
NM_001382789.1:c.3626_3628del	NP_001369718.1:p.Gly1209del
NM_001382790.1:c.3602_3604del	NP_001369719.1:p.Gly1201del
NM_001382791.1:c.3596_3598del	NP_001369720.1:p.Gly1199del
NM_001382792.1:c.3569_3571del	NP_001369721.1:p.Gly1190del
NM_001382793.1:c.3563_3565del	NP_001369722.1:p.Gly1188del
NM_001382794.1:c.3563_3565del	NP_001369723.1:p.Gly1188del
NM_001382795.1:c.3557_3559del	NP_001369724.1:p.Gly1186del
NM_001382796.1:c.3518_3520del	NP_001369725.1:p.Gly1173del
NM_001382797.1:c.3506_3508del	NP_001369726.1:p.Gly1169del
NM_001382798.1:c.3449_3451del	NP_001369727.1:p.Gly1150del
NM_001382799.1:c.3425_3427del	NP_001369728.1:p.Gly1142del
NM_001382800.1:c.3419_3421del	NP_001369729.1:p.Gly1140del
NM_001382801.1:c.3401_3403del	NP_001369730.1:p.Gly1134del
NM_001382802.1:c.3347_3349del	NP_001369731.1:p.Gly1116del
NM_001382803.1:c.*184_*186del	NP_001369732.1:n.*184_*186del
NM_001382804.1:c.2777_2779del	NP_001369733.1:p.Gly926del
NM_001382805.1:c.2654_2656del	NP_001369734.1:p.Gly885del
NM_001382806.1:c.2567_2569del	NP_001369735.1:p.Gly856del
NM_004448.4:c.3605_3607del MANE Select	NP_004439.2:p.Gly1202del
NR_110535.2:n.3843_3845del