Canonical Allele Identifier: CA399310314

Gene: ERBB2

Linked Data

• dbSNP Id: rs1178111397
• MyVariant Identifiers: chr17:g.37883603G>A (hg19) ; chr17:g.39727350G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727350G>A , CM000679.2:g.39727350G>A	GRCh38
NC_000017.10:g.37883603G>A , CM000679.1:g.37883603G>A	GRCh37
NC_000017.9:g.35137129G>A	NCBI36
NG_007503.1:g.44211G>A , LRG_724:g.44211G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3215G>A MANE Select	ENSP00000269571.4:p.Arg1072Lys
ENST00000269571.9:c.3215G>A	ENSP00000269571.4:p.Arg1072Lys
ENST00000406381.6:c.3125G>A	ENSP00000385185.2:p.Arg1042Lys
ENST00000445658.6:c.2387G>A	ENSP00000404047.2:p.Arg796Lys
ENST00000541774.5:c.3170G>A	ENSP00000446466.1:p.Arg1057Lys
ENST00000578373.5:c.*3005G>A	ENSP00000463427.1:n.*3005G>A
ENST00000584450.5:c.3160-339G>A	ENSP00000463714.1:n.3160-339G>A
ENST00000584601.5:c.3125G>A	ENSP00000462438.1:p.Arg1042Lys
NM_001005862.2:c.3125G>A , LRG_724t1:c.3125G>A	NP_001005862.1:p.Arg1042Lys
NM_001289936.1:c.3170G>A , LRG_724t4:c.3170G>A	NP_001276865.1:p.Arg1057Lys
NM_001289937.1:c.3160-339G>A	NP_001276866.1:n.3160-339G>A
NM_004448.3:c.3215G>A , LRG_724t2:c.3215G>A	NP_004439.2:p.Arg1072Lys
NR_110535.1:n.3539G>A
XM_024450641.1:c.3353G>A	XP_024306409.1:p.Arg1118Lys
XM_024450642.1:c.3308G>A	XP_024306410.1:p.Arg1103Lys
XM_024450643.1:c.3263G>A	XP_024306411.1:p.Arg1088Lys
NM_001005862.3:c.3125G>A	NP_001005862.1:p.Arg1042Lys
NM_001289936.2:c.3170G>A	NP_001276865.1:p.Arg1057Lys
NM_001289937.2:c.3160-339G>A	NP_001276866.1:n.3160-339G>A
NM_001382782.1:c.3125G>A	NP_001369711.1:p.Arg1042Lys
NM_001382783.1:c.3125G>A	NP_001369712.1:p.Arg1042Lys
NM_001382784.1:c.3332G>A	NP_001369713.1:p.Arg1111Lys
NM_001382785.1:c.3317G>A	NP_001369714.1:p.Arg1106Lys
NM_001382786.1:c.3296G>A	NP_001369715.1:p.Arg1099Lys
NM_001382787.1:c.3290G>A	NP_001369716.1:p.Arg1097Lys
NM_001382788.1:c.3245G>A	NP_001369717.1:p.Arg1082Lys
NM_001382789.1:c.3236G>A	NP_001369718.1:p.Arg1079Lys
NM_001382790.1:c.3212G>A	NP_001369719.1:p.Arg1071Lys
NM_001382791.1:c.3206G>A	NP_001369720.1:p.Arg1069Lys
NM_001382792.1:c.3179G>A	NP_001369721.1:p.Arg1060Lys
NM_001382793.1:c.3173G>A	NP_001369722.1:p.Arg1058Lys
NM_001382794.1:c.3173G>A	NP_001369723.1:p.Arg1058Lys
NM_001382795.1:c.3167G>A	NP_001369724.1:p.Arg1056Lys
NM_001382796.1:c.3128G>A	NP_001369725.1:p.Arg1043Lys
NM_001382797.1:c.3116G>A	NP_001369726.1:p.Arg1039Lys
NM_001382798.1:c.3059G>A	NP_001369727.1:p.Arg1020Lys
NM_001382799.1:c.3035G>A	NP_001369728.1:p.Arg1012Lys
NM_001382800.1:c.3029G>A	NP_001369729.1:p.Arg1010Lys
NM_001382801.1:c.3011G>A	NP_001369730.1:p.Arg1004Lys
NM_001382802.1:c.2957G>A	NP_001369731.1:p.Arg986Lys
NM_001382803.1:c.3118-339G>A	NP_001369732.1:n.3118-339G>A
NM_001382804.1:c.2387G>A	NP_001369733.1:p.Arg796Lys
NM_001382805.1:c.2264G>A	NP_001369734.1:p.Arg755Lys
NM_001382806.1:c.2177G>A	NP_001369735.1:p.Arg726Lys
NM_004448.4:c.3215G>A MANE Select	NP_004439.2:p.Arg1072Lys
NR_110535.2:n.3453G>A