Canonical Allele Identifier: CA399312898

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143290284
• MyVariant Identifiers: chr17:g.37883980T>A (hg19) ; chr17:g.39727727T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727727T>A , CM000679.2:g.39727727T>A	GRCh38
NC_000017.10:g.37883980T>A , CM000679.1:g.37883980T>A	GRCh37
NC_000017.9:g.35137506T>A	NCBI36
NG_007503.1:g.44588T>A , LRG_724:g.44588T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3451T>A MANE Select	ENSP00000269571.4:p.Ser1151Thr
ENST00000269571.9:c.3451T>A	ENSP00000269571.4:p.Ser1151Thr
ENST00000406381.6:c.3361T>A	ENSP00000385185.2:p.Ser1121Thr
ENST00000445658.6:c.2623T>A	ENSP00000404047.2:p.Ser875Thr
ENST00000541774.5:c.3406T>A	ENSP00000446466.1:p.Ser1136Thr
ENST00000578373.5:c.*3241T>A	ENSP00000463427.1:n.*3241T>A
ENST00000584450.5:c.*30T>A	ENSP00000463714.1:n.*30T>A
ENST00000584601.5:c.3361T>A	ENSP00000462438.1:p.Ser1121Thr
NM_001005862.2:c.3361T>A , LRG_724t1:c.3361T>A	NP_001005862.1:p.Ser1121Thr
NM_001289936.1:c.3406T>A , LRG_724t4:c.3406T>A	NP_001276865.1:p.Ser1136Thr
NM_001289937.1:c.*30T>A	NP_001276866.1:n.*30T>A
NM_004448.3:c.3451T>A , LRG_724t2:c.3451T>A	NP_004439.2:p.Ser1151Thr
NR_110535.1:n.3775T>A
XM_024450641.1:c.3589T>A	XP_024306409.1:p.Ser1197Thr
XM_024450642.1:c.3544T>A	XP_024306410.1:p.Ser1182Thr
XM_024450643.1:c.3499T>A	XP_024306411.1:p.Ser1167Thr
NM_001005862.3:c.3361T>A	NP_001005862.1:p.Ser1121Thr
NM_001289936.2:c.3406T>A	NP_001276865.1:p.Ser1136Thr
NM_001289937.2:c.*30T>A	NP_001276866.1:n.*30T>A
NM_001382782.1:c.3361T>A	NP_001369711.1:p.Ser1121Thr
NM_001382783.1:c.3361T>A	NP_001369712.1:p.Ser1121Thr
NM_001382784.1:c.3568T>A	NP_001369713.1:p.Ser1190Thr
NM_001382785.1:c.3553T>A	NP_001369714.1:p.Ser1185Thr
NM_001382786.1:c.3532T>A	NP_001369715.1:p.Ser1178Thr
NM_001382787.1:c.3526T>A	NP_001369716.1:p.Ser1176Thr
NM_001382788.1:c.3481T>A	NP_001369717.1:p.Ser1161Thr
NM_001382789.1:c.3472T>A	NP_001369718.1:p.Ser1158Thr
NM_001382790.1:c.3448T>A	NP_001369719.1:p.Ser1150Thr
NM_001382791.1:c.3442T>A	NP_001369720.1:p.Ser1148Thr
NM_001382792.1:c.3415T>A	NP_001369721.1:p.Ser1139Thr
NM_001382793.1:c.3409T>A	NP_001369722.1:p.Ser1137Thr
NM_001382794.1:c.3409T>A	NP_001369723.1:p.Ser1137Thr
NM_001382795.1:c.3403T>A	NP_001369724.1:p.Ser1135Thr
NM_001382796.1:c.3364T>A	NP_001369725.1:p.Ser1122Thr
NM_001382797.1:c.3352T>A	NP_001369726.1:p.Ser1118Thr
NM_001382798.1:c.3295T>A	NP_001369727.1:p.Ser1099Thr
NM_001382799.1:c.3271T>A	NP_001369728.1:p.Ser1091Thr
NM_001382800.1:c.3265T>A	NP_001369729.1:p.Ser1089Thr
NM_001382801.1:c.3247T>A	NP_001369730.1:p.Ser1083Thr
NM_001382802.1:c.3193T>A	NP_001369731.1:p.Ser1065Thr
NM_001382803.1:c.*30T>A	NP_001369732.1:n.*30T>A
NM_001382804.1:c.2623T>A	NP_001369733.1:p.Ser875Thr
NM_001382805.1:c.2500T>A	NP_001369734.1:p.Ser834Thr
NM_001382806.1:c.2413T>A	NP_001369735.1:p.Ser805Thr
NM_004448.4:c.3451T>A MANE Select	NP_004439.2:p.Ser1151Thr
NR_110535.2:n.3689T>A