Canonical Allele Identifier: CA399314348

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884190T>G (hg19) ; chr17:g.39727937T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3661T>G MANE Select	ENSP00000269571.4:p.Tyr1221Asp
ENST00000269571.9:c.3661T>G	ENSP00000269571.4:p.Tyr1221Asp
ENST00000406381.6:c.3571T>G	ENSP00000385185.2:p.Tyr1191Asp
ENST00000445658.6:c.2833T>G	ENSP00000404047.2:p.Tyr945Asp
ENST00000541774.5:c.3616T>G	ENSP00000446466.1:p.Tyr1206Asp
ENST00000578373.5:c.*3451T>G	ENSP00000463427.1:n.*3451T>G
ENST00000584450.5:c.*240T>G	ENSP00000463714.1:n.*240T>G
ENST00000584601.5:c.3571T>G	ENSP00000462438.1:p.Tyr1191Asp
NM_001005862.2:c.3571T>G , LRG_724t1:c.3571T>G	NP_001005862.1:p.Tyr1191Asp
NM_001289936.1:c.3616T>G , LRG_724t4:c.3616T>G	NP_001276865.1:p.Tyr1206Asp
NM_001289937.1:c.*240T>G	NP_001276866.1:n.*240T>G
NM_004448.3:c.3661T>G , LRG_724t2:c.3661T>G	NP_004439.2:p.Tyr1221Asp
NR_110535.1:n.3985T>G
XM_024450641.1:c.3799T>G	XP_024306409.1:p.Tyr1267Asp
XM_024450642.1:c.3754T>G	XP_024306410.1:p.Tyr1252Asp
XM_024450643.1:c.3709T>G	XP_024306411.1:p.Tyr1237Asp
NM_001005862.3:c.3571T>G	NP_001005862.1:p.Tyr1191Asp
NM_001289936.2:c.3616T>G	NP_001276865.1:p.Tyr1206Asp
NM_001289937.2:c.*240T>G	NP_001276866.1:n.*240T>G
NM_001382782.1:c.3571T>G	NP_001369711.1:p.Tyr1191Asp
NM_001382783.1:c.3571T>G	NP_001369712.1:p.Tyr1191Asp
NM_001382784.1:c.3778T>G	NP_001369713.1:p.Tyr1260Asp
NM_001382785.1:c.3763T>G	NP_001369714.1:p.Tyr1255Asp
NM_001382786.1:c.3742T>G	NP_001369715.1:p.Tyr1248Asp
NM_001382787.1:c.3736T>G	NP_001369716.1:p.Tyr1246Asp
NM_001382788.1:c.3691T>G	NP_001369717.1:p.Tyr1231Asp
NM_001382789.1:c.3682T>G	NP_001369718.1:p.Tyr1228Asp
NM_001382790.1:c.3658T>G	NP_001369719.1:p.Tyr1220Asp
NM_001382791.1:c.3652T>G	NP_001369720.1:p.Tyr1218Asp
NM_001382792.1:c.3625T>G	NP_001369721.1:p.Tyr1209Asp
NM_001382793.1:c.3619T>G	NP_001369722.1:p.Tyr1207Asp
NM_001382794.1:c.3619T>G	NP_001369723.1:p.Tyr1207Asp
NM_001382795.1:c.3613T>G	NP_001369724.1:p.Tyr1205Asp
NM_001382796.1:c.3574T>G	NP_001369725.1:p.Tyr1192Asp
NM_001382797.1:c.3562T>G	NP_001369726.1:p.Tyr1188Asp
NM_001382798.1:c.3505T>G	NP_001369727.1:p.Tyr1169Asp
NM_001382799.1:c.3481T>G	NP_001369728.1:p.Tyr1161Asp
NM_001382800.1:c.3475T>G	NP_001369729.1:p.Tyr1159Asp
NM_001382801.1:c.3457T>G	NP_001369730.1:p.Tyr1153Asp
NM_001382802.1:c.3403T>G	NP_001369731.1:p.Tyr1135Asp
NM_001382803.1:c.*240T>G	NP_001369732.1:n.*240T>G
NM_001382804.1:c.2833T>G	NP_001369733.1:p.Tyr945Asp
NM_001382805.1:c.2710T>G	NP_001369734.1:p.Tyr904Asp
NM_001382806.1:c.2623T>G	NP_001369735.1:p.Tyr875Asp
NM_004448.4:c.3661T>G MANE Select	NP_004439.2:p.Tyr1221Asp
NR_110535.2:n.3899T>G