Canonical Allele Identifier: CA399314564

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884217C>G (hg19) ; chr17:g.39727964C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727964C>G , CM000679.2:g.39727964C>G	GRCh38
NC_000017.10:g.37884217C>G , CM000679.1:g.37884217C>G	GRCh37
NC_000017.9:g.35137743C>G	NCBI36
NG_007503.1:g.44825C>G , LRG_724:g.44825C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3688C>G MANE Select	ENSP00000269571.4:p.Arg1230Gly
ENST00000269571.9:c.3688C>G	ENSP00000269571.4:p.Arg1230Gly
ENST00000406381.6:c.3598C>G	ENSP00000385185.2:p.Arg1200Gly
ENST00000445658.6:c.2860C>G	ENSP00000404047.2:p.Arg954Gly
ENST00000541774.5:c.3643C>G	ENSP00000446466.1:p.Arg1215Gly
ENST00000578373.5:c.*3478C>G	ENSP00000463427.1:n.*3478C>G
ENST00000584450.5:c.*267C>G	ENSP00000463714.1:n.*267C>G
ENST00000584601.5:c.3598C>G	ENSP00000462438.1:p.Arg1200Gly
NM_001005862.2:c.3598C>G , LRG_724t1:c.3598C>G	NP_001005862.1:p.Arg1200Gly
NM_001289936.1:c.3643C>G , LRG_724t4:c.3643C>G	NP_001276865.1:p.Arg1215Gly
NM_001289937.1:c.*267C>G	NP_001276866.1:n.*267C>G
NM_004448.3:c.3688C>G , LRG_724t2:c.3688C>G	NP_004439.2:p.Arg1230Gly
NR_110535.1:n.4012C>G
XM_024450641.1:c.3826C>G	XP_024306409.1:p.Arg1276Gly
XM_024450642.1:c.3781C>G	XP_024306410.1:p.Arg1261Gly
XM_024450643.1:c.3736C>G	XP_024306411.1:p.Arg1246Gly
NM_001005862.3:c.3598C>G	NP_001005862.1:p.Arg1200Gly
NM_001289936.2:c.3643C>G	NP_001276865.1:p.Arg1215Gly
NM_001289937.2:c.*267C>G	NP_001276866.1:n.*267C>G
NM_001382782.1:c.3598C>G	NP_001369711.1:p.Arg1200Gly
NM_001382783.1:c.3598C>G	NP_001369712.1:p.Arg1200Gly
NM_001382784.1:c.3805C>G	NP_001369713.1:p.Arg1269Gly
NM_001382785.1:c.3790C>G	NP_001369714.1:p.Arg1264Gly
NM_001382786.1:c.3769C>G	NP_001369715.1:p.Arg1257Gly
NM_001382787.1:c.3763C>G	NP_001369716.1:p.Arg1255Gly
NM_001382788.1:c.3718C>G	NP_001369717.1:p.Arg1240Gly
NM_001382789.1:c.3709C>G	NP_001369718.1:p.Arg1237Gly
NM_001382790.1:c.3685C>G	NP_001369719.1:p.Arg1229Gly
NM_001382791.1:c.3679C>G	NP_001369720.1:p.Arg1227Gly
NM_001382792.1:c.3652C>G	NP_001369721.1:p.Arg1218Gly
NM_001382793.1:c.3646C>G	NP_001369722.1:p.Arg1216Gly
NM_001382794.1:c.3646C>G	NP_001369723.1:p.Arg1216Gly
NM_001382795.1:c.3640C>G	NP_001369724.1:p.Arg1214Gly
NM_001382796.1:c.3601C>G	NP_001369725.1:p.Arg1201Gly
NM_001382797.1:c.3589C>G	NP_001369726.1:p.Arg1197Gly
NM_001382798.1:c.3532C>G	NP_001369727.1:p.Arg1178Gly
NM_001382799.1:c.3508C>G	NP_001369728.1:p.Arg1170Gly
NM_001382800.1:c.3502C>G	NP_001369729.1:p.Arg1168Gly
NM_001382801.1:c.3484C>G	NP_001369730.1:p.Arg1162Gly
NM_001382802.1:c.3430C>G	NP_001369731.1:p.Arg1144Gly
NM_001382803.1:c.*267C>G	NP_001369732.1:n.*267C>G
NM_001382804.1:c.2860C>G	NP_001369733.1:p.Arg954Gly
NM_001382805.1:c.2737C>G	NP_001369734.1:p.Arg913Gly
NM_001382806.1:c.2650C>G	NP_001369735.1:p.Arg884Gly
NM_004448.4:c.3688C>G MANE Select	NP_004439.2:p.Arg1230Gly
NR_110535.2:n.3926C>G