Canonical Allele Identifier: CA399310319

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3215G>T MANE Select	ENSP00000269571.4:p.Arg1072Met
ENST00000269571.9:c.3215G>T	ENSP00000269571.4:p.Arg1072Met
ENST00000406381.6:c.3125G>T	ENSP00000385185.2:p.Arg1042Met
ENST00000445658.6:c.2387G>T	ENSP00000404047.2:p.Arg796Met
ENST00000541774.5:c.3170G>T	ENSP00000446466.1:p.Arg1057Met
ENST00000578373.5:c.*3005G>T	ENSP00000463427.1:n.*3005G>T
ENST00000584450.5:c.3160-339G>T	ENSP00000463714.1:n.3160-339G>T
ENST00000584601.5:c.3125G>T	ENSP00000462438.1:p.Arg1042Met
NM_001005862.2:c.3125G>T , LRG_724t1:c.3125G>T	NP_001005862.1:p.Arg1042Met
NM_001289936.1:c.3170G>T , LRG_724t4:c.3170G>T	NP_001276865.1:p.Arg1057Met
NM_001289937.1:c.3160-339G>T	NP_001276866.1:n.3160-339G>T
NM_004448.3:c.3215G>T , LRG_724t2:c.3215G>T	NP_004439.2:p.Arg1072Met
NR_110535.1:n.3539G>T
XM_024450641.1:c.3353G>T	XP_024306409.1:p.Arg1118Met
XM_024450642.1:c.3308G>T	XP_024306410.1:p.Arg1103Met
XM_024450643.1:c.3263G>T	XP_024306411.1:p.Arg1088Met
NM_001005862.3:c.3125G>T	NP_001005862.1:p.Arg1042Met
NM_001289936.2:c.3170G>T	NP_001276865.1:p.Arg1057Met
NM_001289937.2:c.3160-339G>T	NP_001276866.1:n.3160-339G>T
NM_001382782.1:c.3125G>T	NP_001369711.1:p.Arg1042Met
NM_001382783.1:c.3125G>T	NP_001369712.1:p.Arg1042Met
NM_001382784.1:c.3332G>T	NP_001369713.1:p.Arg1111Met
NM_001382785.1:c.3317G>T	NP_001369714.1:p.Arg1106Met
NM_001382786.1:c.3296G>T	NP_001369715.1:p.Arg1099Met
NM_001382787.1:c.3290G>T	NP_001369716.1:p.Arg1097Met
NM_001382788.1:c.3245G>T	NP_001369717.1:p.Arg1082Met
NM_001382789.1:c.3236G>T	NP_001369718.1:p.Arg1079Met
NM_001382790.1:c.3212G>T	NP_001369719.1:p.Arg1071Met
NM_001382791.1:c.3206G>T	NP_001369720.1:p.Arg1069Met
NM_001382792.1:c.3179G>T	NP_001369721.1:p.Arg1060Met
NM_001382793.1:c.3173G>T	NP_001369722.1:p.Arg1058Met
NM_001382794.1:c.3173G>T	NP_001369723.1:p.Arg1058Met
NM_001382795.1:c.3167G>T	NP_001369724.1:p.Arg1056Met
NM_001382796.1:c.3128G>T	NP_001369725.1:p.Arg1043Met
NM_001382797.1:c.3116G>T	NP_001369726.1:p.Arg1039Met
NM_001382798.1:c.3059G>T	NP_001369727.1:p.Arg1020Met
NM_001382799.1:c.3035G>T	NP_001369728.1:p.Arg1012Met
NM_001382800.1:c.3029G>T	NP_001369729.1:p.Arg1010Met
NM_001382801.1:c.3011G>T	NP_001369730.1:p.Arg1004Met
NM_001382802.1:c.2957G>T	NP_001369731.1:p.Arg986Met
NM_001382803.1:c.3118-339G>T	NP_001369732.1:n.3118-339G>T
NM_001382804.1:c.2387G>T	NP_001369733.1:p.Arg796Met
NM_001382805.1:c.2264G>T	NP_001369734.1:p.Arg755Met
NM_001382806.1:c.2177G>T	NP_001369735.1:p.Arg726Met
NM_004448.4:c.3215G>T MANE Select	NP_004439.2:p.Arg1072Met
NR_110535.2:n.3453G>T