Canonical Allele Identifier: CA2733497007

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143235974

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727336_39727338del , CM000679.2:g.39727336_39727338del	GRCh38
NC_000017.10:g.37883589_37883591del , CM000679.1:g.37883589_37883591del	GRCh37
NC_000017.9:g.35137115_35137117del	NCBI36
NG_007503.1:g.44197_44199del , LRG_724:g.44197_44199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3201_3203del MANE Select	ENSP00000269571.4:p.Glu1068del
ENST00000269571.9:c.3201_3203del	ENSP00000269571.4:p.Glu1068del
ENST00000406381.6:c.3111_3113del	ENSP00000385185.2:p.Glu1038del
ENST00000445658.6:c.2373_2375del	ENSP00000404047.2:p.Glu792del
ENST00000541774.5:c.3156_3158del	ENSP00000446466.1:p.Glu1053del
ENST00000578373.5:c.*2991_*2993del	ENSP00000463427.1:n.*2991_*2993del
ENST00000584450.5:c.3159+333_3159+335del	ENSP00000463714.1:n.3159+333_3159+335del
ENST00000584601.5:c.3111_3113del	ENSP00000462438.1:p.Glu1038del
NM_001005862.2:c.3111_3113del , LRG_724t1:c.3111_3113del	NP_001005862.1:p.Glu1038del
NM_001289936.1:c.3156_3158del , LRG_724t4:c.3156_3158del	NP_001276865.1:p.Glu1053del
NM_001289937.1:c.3159+333_3159+335del	NP_001276866.1:n.3159+333_3159+335del
NM_004448.3:c.3201_3203del , LRG_724t2:c.3201_3203del	NP_004439.2:p.Glu1068del
NR_110535.1:n.3525_3527del
XM_024450641.1:c.3339_3341del	XP_024306409.1:p.Glu1114del
XM_024450642.1:c.3294_3296del	XP_024306410.1:p.Glu1099del
XM_024450643.1:c.3249_3251del	XP_024306411.1:p.Glu1084del
NM_001005862.3:c.3111_3113del	NP_001005862.1:p.Glu1038del
NM_001289936.2:c.3156_3158del	NP_001276865.1:p.Glu1053del
NM_001289937.2:c.3159+333_3159+335del	NP_001276866.1:n.3159+333_3159+335del
NM_001382782.1:c.3111_3113del	NP_001369711.1:p.Glu1038del
NM_001382783.1:c.3111_3113del	NP_001369712.1:p.Glu1038del
NM_001382784.1:c.3318_3320del	NP_001369713.1:p.Glu1107del
NM_001382785.1:c.3303_3305del	NP_001369714.1:p.Glu1102del
NM_001382786.1:c.3282_3284del	NP_001369715.1:p.Glu1095del
NM_001382787.1:c.3276_3278del	NP_001369716.1:p.Glu1093del
NM_001382788.1:c.3231_3233del	NP_001369717.1:p.Glu1078del
NM_001382789.1:c.3222_3224del	NP_001369718.1:p.Glu1075del
NM_001382790.1:c.3198_3200del	NP_001369719.1:p.Glu1067del
NM_001382791.1:c.3192_3194del	NP_001369720.1:p.Glu1065del
NM_001382792.1:c.3165_3167del	NP_001369721.1:p.Glu1056del
NM_001382793.1:c.3159_3161del	NP_001369722.1:p.Glu1054del
NM_001382794.1:c.3159_3161del	NP_001369723.1:p.Glu1054del
NM_001382795.1:c.3153_3155del	NP_001369724.1:p.Glu1052del
NM_001382796.1:c.3114_3116del	NP_001369725.1:p.Glu1039del
NM_001382797.1:c.3102_3104del	NP_001369726.1:p.Glu1035del
NM_001382798.1:c.3045_3047del	NP_001369727.1:p.Glu1016del
NM_001382799.1:c.3021_3023del	NP_001369728.1:p.Glu1008del
NM_001382800.1:c.3015_3017del	NP_001369729.1:p.Glu1006del
NM_001382801.1:c.2997_2999del	NP_001369730.1:p.Glu1000del
NM_001382802.1:c.2943_2945del	NP_001369731.1:p.Glu982del
NM_001382803.1:c.3117+333_3117+335del	NP_001369732.1:n.3117+333_3117+335del
NM_001382804.1:c.2373_2375del	NP_001369733.1:p.Glu792del
NM_001382805.1:c.2250_2252del	NP_001369734.1:p.Glu751del
NM_001382806.1:c.2163_2165del	NP_001369735.1:p.Glu722del
NM_004448.4:c.3201_3203del MANE Select	NP_004439.2:p.Glu1068del
NR_110535.2:n.3439_3441del