Canonical Allele Identifier: CA399310438

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143240438
• MyVariant Identifiers: chr17:g.37883624A>T (hg19) ; chr17:g.39727371A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727371A>T , CM000679.2:g.39727371A>T	GRCh38
NC_000017.10:g.37883624A>T , CM000679.1:g.37883624A>T	GRCh37
NC_000017.9:g.35137150A>T	NCBI36
NG_007503.1:g.44232A>T , LRG_724:g.44232A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3236A>T MANE Select	ENSP00000269571.4:p.Glu1079Val
ENST00000269571.9:c.3236A>T	ENSP00000269571.4:p.Glu1079Val
ENST00000406381.6:c.3146A>T	ENSP00000385185.2:p.Glu1049Val
ENST00000445658.6:c.2408A>T	ENSP00000404047.2:p.Glu803Val
ENST00000541774.5:c.3191A>T	ENSP00000446466.1:p.Glu1064Val
ENST00000578373.5:c.*3026A>T	ENSP00000463427.1:n.*3026A>T
ENST00000584450.5:c.3160-318A>T	ENSP00000463714.1:n.3160-318A>T
ENST00000584601.5:c.3146A>T	ENSP00000462438.1:p.Glu1049Val
NM_001005862.2:c.3146A>T , LRG_724t1:c.3146A>T	NP_001005862.1:p.Glu1049Val
NM_001289936.1:c.3191A>T , LRG_724t4:c.3191A>T	NP_001276865.1:p.Glu1064Val
NM_001289937.1:c.3160-318A>T	NP_001276866.1:n.3160-318A>T
NM_004448.3:c.3236A>T , LRG_724t2:c.3236A>T	NP_004439.2:p.Glu1079Val
NR_110535.1:n.3560A>T
XM_024450641.1:c.3374A>T	XP_024306409.1:p.Glu1125Val
XM_024450642.1:c.3329A>T	XP_024306410.1:p.Glu1110Val
XM_024450643.1:c.3284A>T	XP_024306411.1:p.Glu1095Val
NM_001005862.3:c.3146A>T	NP_001005862.1:p.Glu1049Val
NM_001289936.2:c.3191A>T	NP_001276865.1:p.Glu1064Val
NM_001289937.2:c.3160-318A>T	NP_001276866.1:n.3160-318A>T
NM_001382782.1:c.3146A>T	NP_001369711.1:p.Glu1049Val
NM_001382783.1:c.3146A>T	NP_001369712.1:p.Glu1049Val
NM_001382784.1:c.3353A>T	NP_001369713.1:p.Glu1118Val
NM_001382785.1:c.3338A>T	NP_001369714.1:p.Glu1113Val
NM_001382786.1:c.3317A>T	NP_001369715.1:p.Glu1106Val
NM_001382787.1:c.3311A>T	NP_001369716.1:p.Glu1104Val
NM_001382788.1:c.3266A>T	NP_001369717.1:p.Glu1089Val
NM_001382789.1:c.3257A>T	NP_001369718.1:p.Glu1086Val
NM_001382790.1:c.3233A>T	NP_001369719.1:p.Glu1078Val
NM_001382791.1:c.3227A>T	NP_001369720.1:p.Glu1076Val
NM_001382792.1:c.3200A>T	NP_001369721.1:p.Glu1067Val
NM_001382793.1:c.3194A>T	NP_001369722.1:p.Glu1065Val
NM_001382794.1:c.3194A>T	NP_001369723.1:p.Glu1065Val
NM_001382795.1:c.3188A>T	NP_001369724.1:p.Glu1063Val
NM_001382796.1:c.3149A>T	NP_001369725.1:p.Glu1050Val
NM_001382797.1:c.3137A>T	NP_001369726.1:p.Glu1046Val
NM_001382798.1:c.3080A>T	NP_001369727.1:p.Glu1027Val
NM_001382799.1:c.3056A>T	NP_001369728.1:p.Glu1019Val
NM_001382800.1:c.3050A>T	NP_001369729.1:p.Glu1017Val
NM_001382801.1:c.3032A>T	NP_001369730.1:p.Glu1011Val
NM_001382802.1:c.2978A>T	NP_001369731.1:p.Glu993Val
NM_001382803.1:c.3118-318A>T	NP_001369732.1:n.3118-318A>T
NM_001382804.1:c.2408A>T	NP_001369733.1:p.Glu803Val
NM_001382805.1:c.2285A>T	NP_001369734.1:p.Glu762Val
NM_001382806.1:c.2198A>T	NP_001369735.1:p.Glu733Val
NM_004448.4:c.3236A>T MANE Select	NP_004439.2:p.Glu1079Val
NR_110535.2:n.3474A>T