Canonical Allele Identifier: CA399312515

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143250313
• MyVariant Identifiers: chr17:g.37883708G>T (hg19) ; chr17:g.39727455G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727455G>T , CM000679.2:g.39727455G>T	GRCh38
NC_000017.10:g.37883708G>T , CM000679.1:g.37883708G>T	GRCh37
NC_000017.9:g.35137234G>T	NCBI36
NG_007503.1:g.44316G>T , LRG_724:g.44316G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3320G>T MANE Select	ENSP00000269571.4:p.Ser1107Ile
ENST00000269571.9:c.3320G>T	ENSP00000269571.4:p.Ser1107Ile
ENST00000406381.6:c.3230G>T	ENSP00000385185.2:p.Ser1077Ile
ENST00000445658.6:c.2492G>T	ENSP00000404047.2:p.Ser831Ile
ENST00000541774.5:c.3275G>T	ENSP00000446466.1:p.Ser1092Ile
ENST00000578373.5:c.*3110G>T	ENSP00000463427.1:n.*3110G>T
ENST00000584450.5:c.3160-234G>T	ENSP00000463714.1:n.3160-234G>T
ENST00000584601.5:c.3230G>T	ENSP00000462438.1:p.Ser1077Ile
NM_001005862.2:c.3230G>T , LRG_724t1:c.3230G>T	NP_001005862.1:p.Ser1077Ile
NM_001289936.1:c.3275G>T , LRG_724t4:c.3275G>T	NP_001276865.1:p.Ser1092Ile
NM_001289937.1:c.3160-234G>T	NP_001276866.1:n.3160-234G>T
NM_004448.3:c.3320G>T , LRG_724t2:c.3320G>T	NP_004439.2:p.Ser1107Ile
NR_110535.1:n.3644G>T
XM_024450641.1:c.3458G>T	XP_024306409.1:p.Ser1153Ile
XM_024450642.1:c.3413G>T	XP_024306410.1:p.Ser1138Ile
XM_024450643.1:c.3368G>T	XP_024306411.1:p.Ser1123Ile
NM_001005862.3:c.3230G>T	NP_001005862.1:p.Ser1077Ile
NM_001289936.2:c.3275G>T	NP_001276865.1:p.Ser1092Ile
NM_001289937.2:c.3160-234G>T	NP_001276866.1:n.3160-234G>T
NM_001382782.1:c.3230G>T	NP_001369711.1:p.Ser1077Ile
NM_001382783.1:c.3230G>T	NP_001369712.1:p.Ser1077Ile
NM_001382784.1:c.3437G>T	NP_001369713.1:p.Ser1146Ile
NM_001382785.1:c.3422G>T	NP_001369714.1:p.Ser1141Ile
NM_001382786.1:c.3401G>T	NP_001369715.1:p.Ser1134Ile
NM_001382787.1:c.3395G>T	NP_001369716.1:p.Ser1132Ile
NM_001382788.1:c.3350G>T	NP_001369717.1:p.Ser1117Ile
NM_001382789.1:c.3341G>T	NP_001369718.1:p.Ser1114Ile
NM_001382790.1:c.3317G>T	NP_001369719.1:p.Ser1106Ile
NM_001382791.1:c.3311G>T	NP_001369720.1:p.Ser1104Ile
NM_001382792.1:c.3284G>T	NP_001369721.1:p.Ser1095Ile
NM_001382793.1:c.3278G>T	NP_001369722.1:p.Ser1093Ile
NM_001382794.1:c.3278G>T	NP_001369723.1:p.Ser1093Ile
NM_001382795.1:c.3272G>T	NP_001369724.1:p.Ser1091Ile
NM_001382796.1:c.3233G>T	NP_001369725.1:p.Ser1078Ile
NM_001382797.1:c.3221G>T	NP_001369726.1:p.Ser1074Ile
NM_001382798.1:c.3164G>T	NP_001369727.1:p.Ser1055Ile
NM_001382799.1:c.3140G>T	NP_001369728.1:p.Ser1047Ile
NM_001382800.1:c.3134G>T	NP_001369729.1:p.Ser1045Ile
NM_001382801.1:c.3116G>T	NP_001369730.1:p.Ser1039Ile
NM_001382802.1:c.3062G>T	NP_001369731.1:p.Ser1021Ile
NM_001382803.1:c.3118-234G>T	NP_001369732.1:n.3118-234G>T
NM_001382804.1:c.2492G>T	NP_001369733.1:p.Ser831Ile
NM_001382805.1:c.2369G>T	NP_001369734.1:p.Ser790Ile
NM_001382806.1:c.2282G>T	NP_001369735.1:p.Ser761Ile
NM_004448.4:c.3320G>T MANE Select	NP_004439.2:p.Ser1107Ile
NR_110535.2:n.3558G>T