Canonical Allele Identifier: CA399313438

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884070G>T (hg19) ; chr17:g.39727817G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727817G>T , CM000679.2:g.39727817G>T	GRCh38
NC_000017.10:g.37884070G>T , CM000679.1:g.37884070G>T	GRCh37
NC_000017.9:g.35137596G>T	NCBI36
NG_007503.1:g.44678G>T , LRG_724:g.44678G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3541G>T MANE Select	ENSP00000269571.4:p.Val1181Phe
ENST00000269571.9:c.3541G>T	ENSP00000269571.4:p.Val1181Phe
ENST00000406381.6:c.3451G>T	ENSP00000385185.2:p.Val1151Phe
ENST00000445658.6:c.2713G>T	ENSP00000404047.2:p.Val905Phe
ENST00000541774.5:c.3496G>T	ENSP00000446466.1:p.Val1166Phe
ENST00000578373.5:c.*3331G>T	ENSP00000463427.1:n.*3331G>T
ENST00000584450.5:c.*120G>T	ENSP00000463714.1:n.*120G>T
ENST00000584601.5:c.3451G>T	ENSP00000462438.1:p.Val1151Phe
NM_001005862.2:c.3451G>T , LRG_724t1:c.3451G>T	NP_001005862.1:p.Val1151Phe
NM_001289936.1:c.3496G>T , LRG_724t4:c.3496G>T	NP_001276865.1:p.Val1166Phe
NM_001289937.1:c.*120G>T	NP_001276866.1:n.*120G>T
NM_004448.3:c.3541G>T , LRG_724t2:c.3541G>T	NP_004439.2:p.Val1181Phe
NR_110535.1:n.3865G>T
XM_024450641.1:c.3679G>T	XP_024306409.1:p.Val1227Phe
XM_024450642.1:c.3634G>T	XP_024306410.1:p.Val1212Phe
XM_024450643.1:c.3589G>T	XP_024306411.1:p.Val1197Phe
NM_001005862.3:c.3451G>T	NP_001005862.1:p.Val1151Phe
NM_001289936.2:c.3496G>T	NP_001276865.1:p.Val1166Phe
NM_001289937.2:c.*120G>T	NP_001276866.1:n.*120G>T
NM_001382782.1:c.3451G>T	NP_001369711.1:p.Val1151Phe
NM_001382783.1:c.3451G>T	NP_001369712.1:p.Val1151Phe
NM_001382784.1:c.3658G>T	NP_001369713.1:p.Val1220Phe
NM_001382785.1:c.3643G>T	NP_001369714.1:p.Val1215Phe
NM_001382786.1:c.3622G>T	NP_001369715.1:p.Val1208Phe
NM_001382787.1:c.3616G>T	NP_001369716.1:p.Val1206Phe
NM_001382788.1:c.3571G>T	NP_001369717.1:p.Val1191Phe
NM_001382789.1:c.3562G>T	NP_001369718.1:p.Val1188Phe
NM_001382790.1:c.3538G>T	NP_001369719.1:p.Val1180Phe
NM_001382791.1:c.3532G>T	NP_001369720.1:p.Val1178Phe
NM_001382792.1:c.3505G>T	NP_001369721.1:p.Val1169Phe
NM_001382793.1:c.3499G>T	NP_001369722.1:p.Val1167Phe
NM_001382794.1:c.3499G>T	NP_001369723.1:p.Val1167Phe
NM_001382795.1:c.3493G>T	NP_001369724.1:p.Val1165Phe
NM_001382796.1:c.3454G>T	NP_001369725.1:p.Val1152Phe
NM_001382797.1:c.3442G>T	NP_001369726.1:p.Val1148Phe
NM_001382798.1:c.3385G>T	NP_001369727.1:p.Val1129Phe
NM_001382799.1:c.3361G>T	NP_001369728.1:p.Val1121Phe
NM_001382800.1:c.3355G>T	NP_001369729.1:p.Val1119Phe
NM_001382801.1:c.3337G>T	NP_001369730.1:p.Val1113Phe
NM_001382802.1:c.3283G>T	NP_001369731.1:p.Val1095Phe
NM_001382803.1:c.*120G>T	NP_001369732.1:n.*120G>T
NM_001382804.1:c.2713G>T	NP_001369733.1:p.Val905Phe
NM_001382805.1:c.2590G>T	NP_001369734.1:p.Val864Phe
NM_001382806.1:c.2503G>T	NP_001369735.1:p.Val835Phe
NM_004448.4:c.3541G>T MANE Select	NP_004439.2:p.Val1181Phe
NR_110535.2:n.3779G>T