Canonical Allele Identifier: CA399314376

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059871278
• MyVariant Identifiers: chr17:g.37884194A>C (hg19) ; chr17:g.39727941A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727941A>C , CM000679.2:g.39727941A>C	GRCh38
NC_000017.10:g.37884194A>C , CM000679.1:g.37884194A>C	GRCh37
NC_000017.9:g.35137720A>C	NCBI36
NG_007503.1:g.44802A>C , LRG_724:g.44802A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3665A>C MANE Select	ENSP00000269571.4:p.Tyr1222Ser
ENST00000269571.9:c.3665A>C	ENSP00000269571.4:p.Tyr1222Ser
ENST00000406381.6:c.3575A>C	ENSP00000385185.2:p.Tyr1192Ser
ENST00000445658.6:c.2837A>C	ENSP00000404047.2:p.Tyr946Ser
ENST00000541774.5:c.3620A>C	ENSP00000446466.1:p.Tyr1207Ser
ENST00000578373.5:c.*3455A>C	ENSP00000463427.1:n.*3455A>C
ENST00000584450.5:c.*244A>C	ENSP00000463714.1:n.*244A>C
ENST00000584601.5:c.3575A>C	ENSP00000462438.1:p.Tyr1192Ser
NM_001005862.2:c.3575A>C , LRG_724t1:c.3575A>C	NP_001005862.1:p.Tyr1192Ser
NM_001289936.1:c.3620A>C , LRG_724t4:c.3620A>C	NP_001276865.1:p.Tyr1207Ser
NM_001289937.1:c.*244A>C	NP_001276866.1:n.*244A>C
NM_004448.3:c.3665A>C , LRG_724t2:c.3665A>C	NP_004439.2:p.Tyr1222Ser
NR_110535.1:n.3989A>C
XM_024450641.1:c.3803A>C	XP_024306409.1:p.Tyr1268Ser
XM_024450642.1:c.3758A>C	XP_024306410.1:p.Tyr1253Ser
XM_024450643.1:c.3713A>C	XP_024306411.1:p.Tyr1238Ser
NM_001005862.3:c.3575A>C	NP_001005862.1:p.Tyr1192Ser
NM_001289936.2:c.3620A>C	NP_001276865.1:p.Tyr1207Ser
NM_001289937.2:c.*244A>C	NP_001276866.1:n.*244A>C
NM_001382782.1:c.3575A>C	NP_001369711.1:p.Tyr1192Ser
NM_001382783.1:c.3575A>C	NP_001369712.1:p.Tyr1192Ser
NM_001382784.1:c.3782A>C	NP_001369713.1:p.Tyr1261Ser
NM_001382785.1:c.3767A>C	NP_001369714.1:p.Tyr1256Ser
NM_001382786.1:c.3746A>C	NP_001369715.1:p.Tyr1249Ser
NM_001382787.1:c.3740A>C	NP_001369716.1:p.Tyr1247Ser
NM_001382788.1:c.3695A>C	NP_001369717.1:p.Tyr1232Ser
NM_001382789.1:c.3686A>C	NP_001369718.1:p.Tyr1229Ser
NM_001382790.1:c.3662A>C	NP_001369719.1:p.Tyr1221Ser
NM_001382791.1:c.3656A>C	NP_001369720.1:p.Tyr1219Ser
NM_001382792.1:c.3629A>C	NP_001369721.1:p.Tyr1210Ser
NM_001382793.1:c.3623A>C	NP_001369722.1:p.Tyr1208Ser
NM_001382794.1:c.3623A>C	NP_001369723.1:p.Tyr1208Ser
NM_001382795.1:c.3617A>C	NP_001369724.1:p.Tyr1206Ser
NM_001382796.1:c.3578A>C	NP_001369725.1:p.Tyr1193Ser
NM_001382797.1:c.3566A>C	NP_001369726.1:p.Tyr1189Ser
NM_001382798.1:c.3509A>C	NP_001369727.1:p.Tyr1170Ser
NM_001382799.1:c.3485A>C	NP_001369728.1:p.Tyr1162Ser
NM_001382800.1:c.3479A>C	NP_001369729.1:p.Tyr1160Ser
NM_001382801.1:c.3461A>C	NP_001369730.1:p.Tyr1154Ser
NM_001382802.1:c.3407A>C	NP_001369731.1:p.Tyr1136Ser
NM_001382803.1:c.*244A>C	NP_001369732.1:n.*244A>C
NM_001382804.1:c.2837A>C	NP_001369733.1:p.Tyr946Ser
NM_001382805.1:c.2714A>C	NP_001369734.1:p.Tyr905Ser
NM_001382806.1:c.2627A>C	NP_001369735.1:p.Tyr876Ser
NM_004448.4:c.3665A>C MANE Select	NP_004439.2:p.Tyr1222Ser
NR_110535.2:n.3903A>C