Canonical Allele Identifier: CA2576254901

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39727336-AGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727341_39727343del , CM000679.2:g.39727341_39727343del	GRCh38
NC_000017.10:g.37883594_37883596del , CM000679.1:g.37883594_37883596del	GRCh37
NC_000017.9:g.35137120_35137122del	NCBI36
NG_007503.1:g.44202_44204del , LRG_724:g.44202_44204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3206_3208del MANE Select	ENSP00000269571.4:p.Glu1069del
ENST00000269571.9:c.3206_3208del	ENSP00000269571.4:p.Glu1069del
ENST00000406381.6:c.3116_3118del	ENSP00000385185.2:p.Glu1039del
ENST00000445658.6:c.2378_2380del	ENSP00000404047.2:p.Glu793del
ENST00000541774.5:c.3161_3163del	ENSP00000446466.1:p.Glu1054del
ENST00000578373.5:c.*2996_*2998del	ENSP00000463427.1:n.*2996_*2998del
ENST00000584450.5:c.3159+338_3159+340del	ENSP00000463714.1:n.3159+338_3159+340del
ENST00000584601.5:c.3116_3118del	ENSP00000462438.1:p.Glu1039del
NM_001005862.2:c.3116_3118del , LRG_724t1:c.3116_3118del	NP_001005862.1:p.Glu1039del
NM_001289936.1:c.3161_3163del , LRG_724t4:c.3161_3163del	NP_001276865.1:p.Glu1054del
NM_001289937.1:c.3159+338_3159+340del	NP_001276866.1:n.3159+338_3159+340del
NM_004448.3:c.3206_3208del , LRG_724t2:c.3206_3208del	NP_004439.2:p.Glu1069del
NR_110535.1:n.3530_3532del
XM_024450641.1:c.3344_3346del	XP_024306409.1:p.Glu1115del
XM_024450642.1:c.3299_3301del	XP_024306410.1:p.Glu1100del
XM_024450643.1:c.3254_3256del	XP_024306411.1:p.Glu1085del
NM_001005862.3:c.3116_3118del	NP_001005862.1:p.Glu1039del
NM_001289936.2:c.3161_3163del	NP_001276865.1:p.Glu1054del
NM_001289937.2:c.3159+338_3159+340del	NP_001276866.1:n.3159+338_3159+340del
NM_001382782.1:c.3116_3118del	NP_001369711.1:p.Glu1039del
NM_001382783.1:c.3116_3118del	NP_001369712.1:p.Glu1039del
NM_001382784.1:c.3323_3325del	NP_001369713.1:p.Glu1108del
NM_001382785.1:c.3308_3310del	NP_001369714.1:p.Glu1103del
NM_001382786.1:c.3287_3289del	NP_001369715.1:p.Glu1096del
NM_001382787.1:c.3281_3283del	NP_001369716.1:p.Glu1094del
NM_001382788.1:c.3236_3238del	NP_001369717.1:p.Glu1079del
NM_001382789.1:c.3227_3229del	NP_001369718.1:p.Glu1076del
NM_001382790.1:c.3203_3205del	NP_001369719.1:p.Glu1068del
NM_001382791.1:c.3197_3199del	NP_001369720.1:p.Glu1066del
NM_001382792.1:c.3170_3172del	NP_001369721.1:p.Glu1057del
NM_001382793.1:c.3164_3166del	NP_001369722.1:p.Glu1055del
NM_001382794.1:c.3164_3166del	NP_001369723.1:p.Glu1055del
NM_001382795.1:c.3158_3160del	NP_001369724.1:p.Glu1053del
NM_001382796.1:c.3119_3121del	NP_001369725.1:p.Glu1040del
NM_001382797.1:c.3107_3109del	NP_001369726.1:p.Glu1036del
NM_001382798.1:c.3050_3052del	NP_001369727.1:p.Glu1017del
NM_001382799.1:c.3026_3028del	NP_001369728.1:p.Glu1009del
NM_001382800.1:c.3020_3022del	NP_001369729.1:p.Glu1007del
NM_001382801.1:c.3002_3004del	NP_001369730.1:p.Glu1001del
NM_001382802.1:c.2948_2950del	NP_001369731.1:p.Glu983del
NM_001382803.1:c.3117+338_3117+340del	NP_001369732.1:n.3117+338_3117+340del
NM_001382804.1:c.2378_2380del	NP_001369733.1:p.Glu793del
NM_001382805.1:c.2255_2257del	NP_001369734.1:p.Glu752del
NM_001382806.1:c.2168_2170del	NP_001369735.1:p.Glu723del
NM_004448.4:c.3206_3208del MANE Select	NP_004439.2:p.Glu1069del
NR_110535.2:n.3444_3446del