Canonical Allele Identifier: CA2637629311

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727596-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727598del , CM000679.2:g.39727598del	GRCh38
NC_000017.10:g.37883851del , CM000679.1:g.37883851del	GRCh37
NC_000017.9:g.35137377del	NCBI36
NG_007503.1:g.44459del , LRG_724:g.44459del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3412+51del MANE Select	ENSP00000269571.4:n.3412+51del
ENST00000269571.9:c.3412+51del	ENSP00000269571.4:n.3412+51del
ENST00000406381.6:c.3322+51del	ENSP00000385185.2:n.3322+51del
ENST00000445658.6:c.2584+51del	ENSP00000404047.2:n.2584+51del
ENST00000541774.5:c.3367+51del	ENSP00000446466.1:n.3367+51del
ENST00000578373.5:c.*3202+51del	ENSP00000463427.1:n.*3202+51del
ENST00000584450.5:c.3160-91del	ENSP00000463714.1:n.3160-91del
ENST00000584601.5:c.3322+51del	ENSP00000462438.1:n.3322+51del
NM_001005862.2:c.3322+51del , LRG_724t1:c.3322+51del	NP_001005862.1:n.3322+51del
NM_001289936.1:c.3367+51del , LRG_724t4:c.3367+51del	NP_001276865.1:n.3367+51del
NM_001289937.1:c.3160-91del	NP_001276866.1:n.3160-91del
NM_004448.3:c.3412+51del , LRG_724t2:c.3412+51del	NP_004439.2:n.3412+51del
NR_110535.1:n.3736+51del
XM_024450641.1:c.3550+51del	XP_024306409.1:n.3550+51del
XM_024450642.1:c.3505+51del	XP_024306410.1:n.3505+51del
XM_024450643.1:c.3460+51del	XP_024306411.1:n.3460+51del
NM_001005862.3:c.3322+51del	NP_001005862.1:n.3322+51del
NM_001289936.2:c.3367+51del	NP_001276865.1:n.3367+51del
NM_001289937.2:c.3160-91del	NP_001276866.1:n.3160-91del
NM_001382782.1:c.3322+51del	NP_001369711.1:n.3322+51del
NM_001382783.1:c.3322+51del	NP_001369712.1:n.3322+51del
NM_001382784.1:c.3529+51del	NP_001369713.1:n.3529+51del
NM_001382785.1:c.3514+51del	NP_001369714.1:n.3514+51del
NM_001382786.1:c.3493+51del	NP_001369715.1:n.3493+51del
NM_001382787.1:c.3487+51del	NP_001369716.1:n.3487+51del
NM_001382788.1:c.3442+51del	NP_001369717.1:n.3442+51del
NM_001382789.1:c.3433+51del	NP_001369718.1:n.3433+51del
NM_001382790.1:c.3409+51del	NP_001369719.1:n.3409+51del
NM_001382791.1:c.3403+51del	NP_001369720.1:n.3403+51del
NM_001382792.1:c.3376+51del	NP_001369721.1:n.3376+51del
NM_001382793.1:c.3370+51del	NP_001369722.1:n.3370+51del
NM_001382794.1:c.3370+51del	NP_001369723.1:n.3370+51del
NM_001382795.1:c.3364+51del	NP_001369724.1:n.3364+51del
NM_001382796.1:c.3325+51del	NP_001369725.1:n.3325+51del
NM_001382797.1:c.3313+51del	NP_001369726.1:n.3313+51del
NM_001382798.1:c.3256+51del	NP_001369727.1:n.3256+51del
NM_001382799.1:c.3232+51del	NP_001369728.1:n.3232+51del
NM_001382800.1:c.3226+51del	NP_001369729.1:n.3226+51del
NM_001382801.1:c.3208+51del	NP_001369730.1:n.3208+51del
NM_001382802.1:c.3154+51del	NP_001369731.1:n.3154+51del
NM_001382803.1:c.3118-91del	NP_001369732.1:n.3118-91del
NM_001382804.1:c.2584+51del	NP_001369733.1:n.2584+51del
NM_001382805.1:c.2461+51del	NP_001369734.1:n.2461+51del
NM_001382806.1:c.2374+51del	NP_001369735.1:n.2374+51del
NM_004448.4:c.3412+51del MANE Select	NP_004439.2:n.3412+51del
NR_110535.2:n.3650+51del