Canonical Allele Identifier: CA399312711

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143256280
• MyVariant Identifiers: chr17:g.37883761G>T (hg19) ; chr17:g.39727508G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727508G>T , CM000679.2:g.39727508G>T	GRCh38
NC_000017.10:g.37883761G>T , CM000679.1:g.37883761G>T	GRCh37
NC_000017.9:g.35137287G>T	NCBI36
NG_007503.1:g.44369G>T , LRG_724:g.44369G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3373G>T MANE Select	ENSP00000269571.4:p.Asp1125Tyr
ENST00000269571.9:c.3373G>T	ENSP00000269571.4:p.Asp1125Tyr
ENST00000406381.6:c.3283G>T	ENSP00000385185.2:p.Asp1095Tyr
ENST00000445658.6:c.2545G>T	ENSP00000404047.2:p.Asp849Tyr
ENST00000541774.5:c.3328G>T	ENSP00000446466.1:p.Asp1110Tyr
ENST00000578373.5:c.*3163G>T	ENSP00000463427.1:n.*3163G>T
ENST00000584450.5:c.3160-181G>T	ENSP00000463714.1:n.3160-181G>T
ENST00000584601.5:c.3283G>T	ENSP00000462438.1:p.Asp1095Tyr
NM_001005862.2:c.3283G>T , LRG_724t1:c.3283G>T	NP_001005862.1:p.Asp1095Tyr
NM_001289936.1:c.3328G>T , LRG_724t4:c.3328G>T	NP_001276865.1:p.Asp1110Tyr
NM_001289937.1:c.3160-181G>T	NP_001276866.1:n.3160-181G>T
NM_004448.3:c.3373G>T , LRG_724t2:c.3373G>T	NP_004439.2:p.Asp1125Tyr
NR_110535.1:n.3697G>T
XM_024450641.1:c.3511G>T	XP_024306409.1:p.Asp1171Tyr
XM_024450642.1:c.3466G>T	XP_024306410.1:p.Asp1156Tyr
XM_024450643.1:c.3421G>T	XP_024306411.1:p.Asp1141Tyr
NM_001005862.3:c.3283G>T	NP_001005862.1:p.Asp1095Tyr
NM_001289936.2:c.3328G>T	NP_001276865.1:p.Asp1110Tyr
NM_001289937.2:c.3160-181G>T	NP_001276866.1:n.3160-181G>T
NM_001382782.1:c.3283G>T	NP_001369711.1:p.Asp1095Tyr
NM_001382783.1:c.3283G>T	NP_001369712.1:p.Asp1095Tyr
NM_001382784.1:c.3490G>T	NP_001369713.1:p.Asp1164Tyr
NM_001382785.1:c.3475G>T	NP_001369714.1:p.Asp1159Tyr
NM_001382786.1:c.3454G>T	NP_001369715.1:p.Asp1152Tyr
NM_001382787.1:c.3448G>T	NP_001369716.1:p.Asp1150Tyr
NM_001382788.1:c.3403G>T	NP_001369717.1:p.Asp1135Tyr
NM_001382789.1:c.3394G>T	NP_001369718.1:p.Asp1132Tyr
NM_001382790.1:c.3370G>T	NP_001369719.1:p.Asp1124Tyr
NM_001382791.1:c.3364G>T	NP_001369720.1:p.Asp1122Tyr
NM_001382792.1:c.3337G>T	NP_001369721.1:p.Asp1113Tyr
NM_001382793.1:c.3331G>T	NP_001369722.1:p.Asp1111Tyr
NM_001382794.1:c.3331G>T	NP_001369723.1:p.Asp1111Tyr
NM_001382795.1:c.3325G>T	NP_001369724.1:p.Asp1109Tyr
NM_001382796.1:c.3286G>T	NP_001369725.1:p.Asp1096Tyr
NM_001382797.1:c.3274G>T	NP_001369726.1:p.Asp1092Tyr
NM_001382798.1:c.3217G>T	NP_001369727.1:p.Asp1073Tyr
NM_001382799.1:c.3193G>T	NP_001369728.1:p.Asp1065Tyr
NM_001382800.1:c.3187G>T	NP_001369729.1:p.Asp1063Tyr
NM_001382801.1:c.3169G>T	NP_001369730.1:p.Asp1057Tyr
NM_001382802.1:c.3115G>T	NP_001369731.1:p.Asp1039Tyr
NM_001382803.1:c.3118-181G>T	NP_001369732.1:n.3118-181G>T
NM_001382804.1:c.2545G>T	NP_001369733.1:p.Asp849Tyr
NM_001382805.1:c.2422G>T	NP_001369734.1:p.Asp808Tyr
NM_001382806.1:c.2335G>T	NP_001369735.1:p.Asp779Tyr
NM_004448.4:c.3373G>T MANE Select	NP_004439.2:p.Asp1125Tyr
NR_110535.2:n.3611G>T