Canonical Allele Identifier: CA399314157

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884166T>G (hg19) ; chr17:g.39727913T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727913T>G , CM000679.2:g.39727913T>G	GRCh38
NC_000017.10:g.37884166T>G , CM000679.1:g.37884166T>G	GRCh37
NC_000017.9:g.35137692T>G	NCBI36
NG_007503.1:g.44774T>G , LRG_724:g.44774T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3637T>G MANE Select	ENSP00000269571.4:p.Phe1213Val
ENST00000269571.9:c.3637T>G	ENSP00000269571.4:p.Phe1213Val
ENST00000406381.6:c.3547T>G	ENSP00000385185.2:p.Phe1183Val
ENST00000445658.6:c.2809T>G	ENSP00000404047.2:p.Phe937Val
ENST00000541774.5:c.3592T>G	ENSP00000446466.1:p.Phe1198Val
ENST00000578373.5:c.*3427T>G	ENSP00000463427.1:n.*3427T>G
ENST00000584450.5:c.*216T>G	ENSP00000463714.1:n.*216T>G
ENST00000584601.5:c.3547T>G	ENSP00000462438.1:p.Phe1183Val
NM_001005862.2:c.3547T>G , LRG_724t1:c.3547T>G	NP_001005862.1:p.Phe1183Val
NM_001289936.1:c.3592T>G , LRG_724t4:c.3592T>G	NP_001276865.1:p.Phe1198Val
NM_001289937.1:c.*216T>G	NP_001276866.1:n.*216T>G
NM_004448.3:c.3637T>G , LRG_724t2:c.3637T>G	NP_004439.2:p.Phe1213Val
NR_110535.1:n.3961T>G
XM_024450641.1:c.3775T>G	XP_024306409.1:p.Phe1259Val
XM_024450642.1:c.3730T>G	XP_024306410.1:p.Phe1244Val
XM_024450643.1:c.3685T>G	XP_024306411.1:p.Phe1229Val
NM_001005862.3:c.3547T>G	NP_001005862.1:p.Phe1183Val
NM_001289936.2:c.3592T>G	NP_001276865.1:p.Phe1198Val
NM_001289937.2:c.*216T>G	NP_001276866.1:n.*216T>G
NM_001382782.1:c.3547T>G	NP_001369711.1:p.Phe1183Val
NM_001382783.1:c.3547T>G	NP_001369712.1:p.Phe1183Val
NM_001382784.1:c.3754T>G	NP_001369713.1:p.Phe1252Val
NM_001382785.1:c.3739T>G	NP_001369714.1:p.Phe1247Val
NM_001382786.1:c.3718T>G	NP_001369715.1:p.Phe1240Val
NM_001382787.1:c.3712T>G	NP_001369716.1:p.Phe1238Val
NM_001382788.1:c.3667T>G	NP_001369717.1:p.Phe1223Val
NM_001382789.1:c.3658T>G	NP_001369718.1:p.Phe1220Val
NM_001382790.1:c.3634T>G	NP_001369719.1:p.Phe1212Val
NM_001382791.1:c.3628T>G	NP_001369720.1:p.Phe1210Val
NM_001382792.1:c.3601T>G	NP_001369721.1:p.Phe1201Val
NM_001382793.1:c.3595T>G	NP_001369722.1:p.Phe1199Val
NM_001382794.1:c.3595T>G	NP_001369723.1:p.Phe1199Val
NM_001382795.1:c.3589T>G	NP_001369724.1:p.Phe1197Val
NM_001382796.1:c.3550T>G	NP_001369725.1:p.Phe1184Val
NM_001382797.1:c.3538T>G	NP_001369726.1:p.Phe1180Val
NM_001382798.1:c.3481T>G	NP_001369727.1:p.Phe1161Val
NM_001382799.1:c.3457T>G	NP_001369728.1:p.Phe1153Val
NM_001382800.1:c.3451T>G	NP_001369729.1:p.Phe1151Val
NM_001382801.1:c.3433T>G	NP_001369730.1:p.Phe1145Val
NM_001382802.1:c.3379T>G	NP_001369731.1:p.Phe1127Val
NM_001382803.1:c.*216T>G	NP_001369732.1:n.*216T>G
NM_001382804.1:c.2809T>G	NP_001369733.1:p.Phe937Val
NM_001382805.1:c.2686T>G	NP_001369734.1:p.Phe896Val
NM_001382806.1:c.2599T>G	NP_001369735.1:p.Phe867Val
NM_004448.4:c.3637T>G MANE Select	NP_004439.2:p.Phe1213Val
NR_110535.2:n.3875T>G