Canonical Allele Identifier: CA399312779

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3400A>T MANE Select	ENSP00000269571.4:p.Ser1134Cys
ENST00000269571.9:c.3400A>T	ENSP00000269571.4:p.Ser1134Cys
ENST00000406381.6:c.3310A>T	ENSP00000385185.2:p.Ser1104Cys
ENST00000445658.6:c.2572A>T	ENSP00000404047.2:p.Ser858Cys
ENST00000541774.5:c.3355A>T	ENSP00000446466.1:p.Ser1119Cys
ENST00000578373.5:c.*3190A>T	ENSP00000463427.1:n.*3190A>T
ENST00000584450.5:c.3160-154A>T	ENSP00000463714.1:n.3160-154A>T
ENST00000584601.5:c.3310A>T	ENSP00000462438.1:p.Ser1104Cys
NM_001005862.2:c.3310A>T , LRG_724t1:c.3310A>T	NP_001005862.1:p.Ser1104Cys
NM_001289936.1:c.3355A>T , LRG_724t4:c.3355A>T	NP_001276865.1:p.Ser1119Cys
NM_001289937.1:c.3160-154A>T	NP_001276866.1:n.3160-154A>T
NM_004448.3:c.3400A>T , LRG_724t2:c.3400A>T	NP_004439.2:p.Ser1134Cys
NR_110535.1:n.3724A>T
XM_024450641.1:c.3538A>T	XP_024306409.1:p.Ser1180Cys
XM_024450642.1:c.3493A>T	XP_024306410.1:p.Ser1165Cys
XM_024450643.1:c.3448A>T	XP_024306411.1:p.Ser1150Cys
NM_001005862.3:c.3310A>T	NP_001005862.1:p.Ser1104Cys
NM_001289936.2:c.3355A>T	NP_001276865.1:p.Ser1119Cys
NM_001289937.2:c.3160-154A>T	NP_001276866.1:n.3160-154A>T
NM_001382782.1:c.3310A>T	NP_001369711.1:p.Ser1104Cys
NM_001382783.1:c.3310A>T	NP_001369712.1:p.Ser1104Cys
NM_001382784.1:c.3517A>T	NP_001369713.1:p.Ser1173Cys
NM_001382785.1:c.3502A>T	NP_001369714.1:p.Ser1168Cys
NM_001382786.1:c.3481A>T	NP_001369715.1:p.Ser1161Cys
NM_001382787.1:c.3475A>T	NP_001369716.1:p.Ser1159Cys
NM_001382788.1:c.3430A>T	NP_001369717.1:p.Ser1144Cys
NM_001382789.1:c.3421A>T	NP_001369718.1:p.Ser1141Cys
NM_001382790.1:c.3397A>T	NP_001369719.1:p.Ser1133Cys
NM_001382791.1:c.3391A>T	NP_001369720.1:p.Ser1131Cys
NM_001382792.1:c.3364A>T	NP_001369721.1:p.Ser1122Cys
NM_001382793.1:c.3358A>T	NP_001369722.1:p.Ser1120Cys
NM_001382794.1:c.3358A>T	NP_001369723.1:p.Ser1120Cys
NM_001382795.1:c.3352A>T	NP_001369724.1:p.Ser1118Cys
NM_001382796.1:c.3313A>T	NP_001369725.1:p.Ser1105Cys
NM_001382797.1:c.3301A>T	NP_001369726.1:p.Ser1101Cys
NM_001382798.1:c.3244A>T	NP_001369727.1:p.Ser1082Cys
NM_001382799.1:c.3220A>T	NP_001369728.1:p.Ser1074Cys
NM_001382800.1:c.3214A>T	NP_001369729.1:p.Ser1072Cys
NM_001382801.1:c.3196A>T	NP_001369730.1:p.Ser1066Cys
NM_001382802.1:c.3142A>T	NP_001369731.1:p.Ser1048Cys
NM_001382803.1:c.3118-154A>T	NP_001369732.1:n.3118-154A>T
NM_001382804.1:c.2572A>T	NP_001369733.1:p.Ser858Cys
NM_001382805.1:c.2449A>T	NP_001369734.1:p.Ser817Cys
NM_001382806.1:c.2362A>T	NP_001369735.1:p.Ser788Cys
NM_004448.4:c.3400A>T MANE Select	NP_004439.2:p.Ser1134Cys
NR_110535.2:n.3638A>T