Canonical Allele Identifier: CA399313891

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143306660
• MyVariant Identifiers: chr17:g.37884130G>C (hg19) ; chr17:g.39727877G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727877G>C , CM000679.2:g.39727877G>C	GRCh38
NC_000017.10:g.37884130G>C , CM000679.1:g.37884130G>C	GRCh37
NC_000017.9:g.35137656G>C	NCBI36
NG_007503.1:g.44738G>C , LRG_724:g.44738G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3601G>C MANE Select	ENSP00000269571.4:p.Gly1201Arg
ENST00000269571.9:c.3601G>C	ENSP00000269571.4:p.Gly1201Arg
ENST00000406381.6:c.3511G>C	ENSP00000385185.2:p.Gly1171Arg
ENST00000445658.6:c.2773G>C	ENSP00000404047.2:p.Gly925Arg
ENST00000541774.5:c.3556G>C	ENSP00000446466.1:p.Gly1186Arg
ENST00000578373.5:c.*3391G>C	ENSP00000463427.1:n.*3391G>C
ENST00000584450.5:c.*180G>C	ENSP00000463714.1:n.*180G>C
ENST00000584601.5:c.3511G>C	ENSP00000462438.1:p.Gly1171Arg
NM_001005862.2:c.3511G>C , LRG_724t1:c.3511G>C	NP_001005862.1:p.Gly1171Arg
NM_001289936.1:c.3556G>C , LRG_724t4:c.3556G>C	NP_001276865.1:p.Gly1186Arg
NM_001289937.1:c.*180G>C	NP_001276866.1:n.*180G>C
NM_004448.3:c.3601G>C , LRG_724t2:c.3601G>C	NP_004439.2:p.Gly1201Arg
NR_110535.1:n.3925G>C
XM_024450641.1:c.3739G>C	XP_024306409.1:p.Gly1247Arg
XM_024450642.1:c.3694G>C	XP_024306410.1:p.Gly1232Arg
XM_024450643.1:c.3649G>C	XP_024306411.1:p.Gly1217Arg
NM_001005862.3:c.3511G>C	NP_001005862.1:p.Gly1171Arg
NM_001289936.2:c.3556G>C	NP_001276865.1:p.Gly1186Arg
NM_001289937.2:c.*180G>C	NP_001276866.1:n.*180G>C
NM_001382782.1:c.3511G>C	NP_001369711.1:p.Gly1171Arg
NM_001382783.1:c.3511G>C	NP_001369712.1:p.Gly1171Arg
NM_001382784.1:c.3718G>C	NP_001369713.1:p.Gly1240Arg
NM_001382785.1:c.3703G>C	NP_001369714.1:p.Gly1235Arg
NM_001382786.1:c.3682G>C	NP_001369715.1:p.Gly1228Arg
NM_001382787.1:c.3676G>C	NP_001369716.1:p.Gly1226Arg
NM_001382788.1:c.3631G>C	NP_001369717.1:p.Gly1211Arg
NM_001382789.1:c.3622G>C	NP_001369718.1:p.Gly1208Arg
NM_001382790.1:c.3598G>C	NP_001369719.1:p.Gly1200Arg
NM_001382791.1:c.3592G>C	NP_001369720.1:p.Gly1198Arg
NM_001382792.1:c.3565G>C	NP_001369721.1:p.Gly1189Arg
NM_001382793.1:c.3559G>C	NP_001369722.1:p.Gly1187Arg
NM_001382794.1:c.3559G>C	NP_001369723.1:p.Gly1187Arg
NM_001382795.1:c.3553G>C	NP_001369724.1:p.Gly1185Arg
NM_001382796.1:c.3514G>C	NP_001369725.1:p.Gly1172Arg
NM_001382797.1:c.3502G>C	NP_001369726.1:p.Gly1168Arg
NM_001382798.1:c.3445G>C	NP_001369727.1:p.Gly1149Arg
NM_001382799.1:c.3421G>C	NP_001369728.1:p.Gly1141Arg
NM_001382800.1:c.3415G>C	NP_001369729.1:p.Gly1139Arg
NM_001382801.1:c.3397G>C	NP_001369730.1:p.Gly1133Arg
NM_001382802.1:c.3343G>C	NP_001369731.1:p.Gly1115Arg
NM_001382803.1:c.*180G>C	NP_001369732.1:n.*180G>C
NM_001382804.1:c.2773G>C	NP_001369733.1:p.Gly925Arg
NM_001382805.1:c.2650G>C	NP_001369734.1:p.Gly884Arg
NM_001382806.1:c.2563G>C	NP_001369735.1:p.Gly855Arg
NM_004448.4:c.3601G>C MANE Select	NP_004439.2:p.Gly1201Arg
NR_110535.2:n.3839G>C