Canonical Allele Identifier: CA399312777

Gene: ERBB2

Linked Data

• dbSNP Id: rs1166464063
• MyVariant Identifiers: chr17:g.37883788A>C (hg19) ; chr17:g.39727535A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727535A>C , CM000679.2:g.39727535A>C	GRCh38
NC_000017.10:g.37883788A>C , CM000679.1:g.37883788A>C	GRCh37
NC_000017.9:g.35137314A>C	NCBI36
NG_007503.1:g.44396A>C , LRG_724:g.44396A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3400A>C MANE Select	ENSP00000269571.4:p.Ser1134Arg
ENST00000269571.9:c.3400A>C	ENSP00000269571.4:p.Ser1134Arg
ENST00000406381.6:c.3310A>C	ENSP00000385185.2:p.Ser1104Arg
ENST00000445658.6:c.2572A>C	ENSP00000404047.2:p.Ser858Arg
ENST00000541774.5:c.3355A>C	ENSP00000446466.1:p.Ser1119Arg
ENST00000578373.5:c.*3190A>C	ENSP00000463427.1:n.*3190A>C
ENST00000584450.5:c.3160-154A>C	ENSP00000463714.1:n.3160-154A>C
ENST00000584601.5:c.3310A>C	ENSP00000462438.1:p.Ser1104Arg
NM_001005862.2:c.3310A>C , LRG_724t1:c.3310A>C	NP_001005862.1:p.Ser1104Arg
NM_001289936.1:c.3355A>C , LRG_724t4:c.3355A>C	NP_001276865.1:p.Ser1119Arg
NM_001289937.1:c.3160-154A>C	NP_001276866.1:n.3160-154A>C
NM_004448.3:c.3400A>C , LRG_724t2:c.3400A>C	NP_004439.2:p.Ser1134Arg
NR_110535.1:n.3724A>C
XM_024450641.1:c.3538A>C	XP_024306409.1:p.Ser1180Arg
XM_024450642.1:c.3493A>C	XP_024306410.1:p.Ser1165Arg
XM_024450643.1:c.3448A>C	XP_024306411.1:p.Ser1150Arg
NM_001005862.3:c.3310A>C	NP_001005862.1:p.Ser1104Arg
NM_001289936.2:c.3355A>C	NP_001276865.1:p.Ser1119Arg
NM_001289937.2:c.3160-154A>C	NP_001276866.1:n.3160-154A>C
NM_001382782.1:c.3310A>C	NP_001369711.1:p.Ser1104Arg
NM_001382783.1:c.3310A>C	NP_001369712.1:p.Ser1104Arg
NM_001382784.1:c.3517A>C	NP_001369713.1:p.Ser1173Arg
NM_001382785.1:c.3502A>C	NP_001369714.1:p.Ser1168Arg
NM_001382786.1:c.3481A>C	NP_001369715.1:p.Ser1161Arg
NM_001382787.1:c.3475A>C	NP_001369716.1:p.Ser1159Arg
NM_001382788.1:c.3430A>C	NP_001369717.1:p.Ser1144Arg
NM_001382789.1:c.3421A>C	NP_001369718.1:p.Ser1141Arg
NM_001382790.1:c.3397A>C	NP_001369719.1:p.Ser1133Arg
NM_001382791.1:c.3391A>C	NP_001369720.1:p.Ser1131Arg
NM_001382792.1:c.3364A>C	NP_001369721.1:p.Ser1122Arg
NM_001382793.1:c.3358A>C	NP_001369722.1:p.Ser1120Arg
NM_001382794.1:c.3358A>C	NP_001369723.1:p.Ser1120Arg
NM_001382795.1:c.3352A>C	NP_001369724.1:p.Ser1118Arg
NM_001382796.1:c.3313A>C	NP_001369725.1:p.Ser1105Arg
NM_001382797.1:c.3301A>C	NP_001369726.1:p.Ser1101Arg
NM_001382798.1:c.3244A>C	NP_001369727.1:p.Ser1082Arg
NM_001382799.1:c.3220A>C	NP_001369728.1:p.Ser1074Arg
NM_001382800.1:c.3214A>C	NP_001369729.1:p.Ser1072Arg
NM_001382801.1:c.3196A>C	NP_001369730.1:p.Ser1066Arg
NM_001382802.1:c.3142A>C	NP_001369731.1:p.Ser1048Arg
NM_001382803.1:c.3118-154A>C	NP_001369732.1:n.3118-154A>C
NM_001382804.1:c.2572A>C	NP_001369733.1:p.Ser858Arg
NM_001382805.1:c.2449A>C	NP_001369734.1:p.Ser817Arg
NM_001382806.1:c.2362A>C	NP_001369735.1:p.Ser788Arg
NM_004448.4:c.3400A>C MANE Select	NP_004439.2:p.Ser1134Arg
NR_110535.2:n.3638A>C