Canonical Allele Identifier: CA399314344

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143312859
• MyVariant Identifiers: chr17:g.37884190T>A (hg19) ; chr17:g.39727937T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727937T>A , CM000679.2:g.39727937T>A	GRCh38
NC_000017.10:g.37884190T>A , CM000679.1:g.37884190T>A	GRCh37
NC_000017.9:g.35137716T>A	NCBI36
NG_007503.1:g.44798T>A , LRG_724:g.44798T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3661T>A MANE Select	ENSP00000269571.4:p.Tyr1221Asn
ENST00000269571.9:c.3661T>A	ENSP00000269571.4:p.Tyr1221Asn
ENST00000406381.6:c.3571T>A	ENSP00000385185.2:p.Tyr1191Asn
ENST00000445658.6:c.2833T>A	ENSP00000404047.2:p.Tyr945Asn
ENST00000541774.5:c.3616T>A	ENSP00000446466.1:p.Tyr1206Asn
ENST00000578373.5:c.*3451T>A	ENSP00000463427.1:n.*3451T>A
ENST00000584450.5:c.*240T>A	ENSP00000463714.1:n.*240T>A
ENST00000584601.5:c.3571T>A	ENSP00000462438.1:p.Tyr1191Asn
NM_001005862.2:c.3571T>A , LRG_724t1:c.3571T>A	NP_001005862.1:p.Tyr1191Asn
NM_001289936.1:c.3616T>A , LRG_724t4:c.3616T>A	NP_001276865.1:p.Tyr1206Asn
NM_001289937.1:c.*240T>A	NP_001276866.1:n.*240T>A
NM_004448.3:c.3661T>A , LRG_724t2:c.3661T>A	NP_004439.2:p.Tyr1221Asn
NR_110535.1:n.3985T>A
XM_024450641.1:c.3799T>A	XP_024306409.1:p.Tyr1267Asn
XM_024450642.1:c.3754T>A	XP_024306410.1:p.Tyr1252Asn
XM_024450643.1:c.3709T>A	XP_024306411.1:p.Tyr1237Asn
NM_001005862.3:c.3571T>A	NP_001005862.1:p.Tyr1191Asn
NM_001289936.2:c.3616T>A	NP_001276865.1:p.Tyr1206Asn
NM_001289937.2:c.*240T>A	NP_001276866.1:n.*240T>A
NM_001382782.1:c.3571T>A	NP_001369711.1:p.Tyr1191Asn
NM_001382783.1:c.3571T>A	NP_001369712.1:p.Tyr1191Asn
NM_001382784.1:c.3778T>A	NP_001369713.1:p.Tyr1260Asn
NM_001382785.1:c.3763T>A	NP_001369714.1:p.Tyr1255Asn
NM_001382786.1:c.3742T>A	NP_001369715.1:p.Tyr1248Asn
NM_001382787.1:c.3736T>A	NP_001369716.1:p.Tyr1246Asn
NM_001382788.1:c.3691T>A	NP_001369717.1:p.Tyr1231Asn
NM_001382789.1:c.3682T>A	NP_001369718.1:p.Tyr1228Asn
NM_001382790.1:c.3658T>A	NP_001369719.1:p.Tyr1220Asn
NM_001382791.1:c.3652T>A	NP_001369720.1:p.Tyr1218Asn
NM_001382792.1:c.3625T>A	NP_001369721.1:p.Tyr1209Asn
NM_001382793.1:c.3619T>A	NP_001369722.1:p.Tyr1207Asn
NM_001382794.1:c.3619T>A	NP_001369723.1:p.Tyr1207Asn
NM_001382795.1:c.3613T>A	NP_001369724.1:p.Tyr1205Asn
NM_001382796.1:c.3574T>A	NP_001369725.1:p.Tyr1192Asn
NM_001382797.1:c.3562T>A	NP_001369726.1:p.Tyr1188Asn
NM_001382798.1:c.3505T>A	NP_001369727.1:p.Tyr1169Asn
NM_001382799.1:c.3481T>A	NP_001369728.1:p.Tyr1161Asn
NM_001382800.1:c.3475T>A	NP_001369729.1:p.Tyr1159Asn
NM_001382801.1:c.3457T>A	NP_001369730.1:p.Tyr1153Asn
NM_001382802.1:c.3403T>A	NP_001369731.1:p.Tyr1135Asn
NM_001382803.1:c.*240T>A	NP_001369732.1:n.*240T>A
NM_001382804.1:c.2833T>A	NP_001369733.1:p.Tyr945Asn
NM_001382805.1:c.2710T>A	NP_001369734.1:p.Tyr904Asn
NM_001382806.1:c.2623T>A	NP_001369735.1:p.Tyr875Asn
NM_004448.4:c.3661T>A MANE Select	NP_004439.2:p.Tyr1221Asn
NR_110535.2:n.3899T>A