Canonical Allele Identifier: CA399313901

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143306855
• MyVariant Identifiers: chr17:g.37884131G>C (hg19) ; chr17:g.39727878G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727878G>C , CM000679.2:g.39727878G>C	GRCh38
NC_000017.10:g.37884131G>C , CM000679.1:g.37884131G>C	GRCh37
NC_000017.9:g.35137657G>C	NCBI36
NG_007503.1:g.44739G>C , LRG_724:g.44739G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3602G>C MANE Select	ENSP00000269571.4:p.Gly1201Ala
ENST00000269571.9:c.3602G>C	ENSP00000269571.4:p.Gly1201Ala
ENST00000406381.6:c.3512G>C	ENSP00000385185.2:p.Gly1171Ala
ENST00000445658.6:c.2774G>C	ENSP00000404047.2:p.Gly925Ala
ENST00000541774.5:c.3557G>C	ENSP00000446466.1:p.Gly1186Ala
ENST00000578373.5:c.*3392G>C	ENSP00000463427.1:n.*3392G>C
ENST00000584450.5:c.*181G>C	ENSP00000463714.1:n.*181G>C
ENST00000584601.5:c.3512G>C	ENSP00000462438.1:p.Gly1171Ala
NM_001005862.2:c.3512G>C , LRG_724t1:c.3512G>C	NP_001005862.1:p.Gly1171Ala
NM_001289936.1:c.3557G>C , LRG_724t4:c.3557G>C	NP_001276865.1:p.Gly1186Ala
NM_001289937.1:c.*181G>C	NP_001276866.1:n.*181G>C
NM_004448.3:c.3602G>C , LRG_724t2:c.3602G>C	NP_004439.2:p.Gly1201Ala
NR_110535.1:n.3926G>C
XM_024450641.1:c.3740G>C	XP_024306409.1:p.Gly1247Ala
XM_024450642.1:c.3695G>C	XP_024306410.1:p.Gly1232Ala
XM_024450643.1:c.3650G>C	XP_024306411.1:p.Gly1217Ala
NM_001005862.3:c.3512G>C	NP_001005862.1:p.Gly1171Ala
NM_001289936.2:c.3557G>C	NP_001276865.1:p.Gly1186Ala
NM_001289937.2:c.*181G>C	NP_001276866.1:n.*181G>C
NM_001382782.1:c.3512G>C	NP_001369711.1:p.Gly1171Ala
NM_001382783.1:c.3512G>C	NP_001369712.1:p.Gly1171Ala
NM_001382784.1:c.3719G>C	NP_001369713.1:p.Gly1240Ala
NM_001382785.1:c.3704G>C	NP_001369714.1:p.Gly1235Ala
NM_001382786.1:c.3683G>C	NP_001369715.1:p.Gly1228Ala
NM_001382787.1:c.3677G>C	NP_001369716.1:p.Gly1226Ala
NM_001382788.1:c.3632G>C	NP_001369717.1:p.Gly1211Ala
NM_001382789.1:c.3623G>C	NP_001369718.1:p.Gly1208Ala
NM_001382790.1:c.3599G>C	NP_001369719.1:p.Gly1200Ala
NM_001382791.1:c.3593G>C	NP_001369720.1:p.Gly1198Ala
NM_001382792.1:c.3566G>C	NP_001369721.1:p.Gly1189Ala
NM_001382793.1:c.3560G>C	NP_001369722.1:p.Gly1187Ala
NM_001382794.1:c.3560G>C	NP_001369723.1:p.Gly1187Ala
NM_001382795.1:c.3554G>C	NP_001369724.1:p.Gly1185Ala
NM_001382796.1:c.3515G>C	NP_001369725.1:p.Gly1172Ala
NM_001382797.1:c.3503G>C	NP_001369726.1:p.Gly1168Ala
NM_001382798.1:c.3446G>C	NP_001369727.1:p.Gly1149Ala
NM_001382799.1:c.3422G>C	NP_001369728.1:p.Gly1141Ala
NM_001382800.1:c.3416G>C	NP_001369729.1:p.Gly1139Ala
NM_001382801.1:c.3398G>C	NP_001369730.1:p.Gly1133Ala
NM_001382802.1:c.3344G>C	NP_001369731.1:p.Gly1115Ala
NM_001382803.1:c.*181G>C	NP_001369732.1:n.*181G>C
NM_001382804.1:c.2774G>C	NP_001369733.1:p.Gly925Ala
NM_001382805.1:c.2651G>C	NP_001369734.1:p.Gly884Ala
NM_001382806.1:c.2564G>C	NP_001369735.1:p.Gly855Ala
NM_004448.4:c.3602G>C MANE Select	NP_004439.2:p.Gly1201Ala
NR_110535.2:n.3840G>C