Canonical Allele Identifier: CA399310566

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143243107
• MyVariant Identifiers: chr17:g.37883645T>A (hg19) ; chr17:g.39727392T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727392T>A , CM000679.2:g.39727392T>A	GRCh38
NC_000017.10:g.37883645T>A , CM000679.1:g.37883645T>A	GRCh37
NC_000017.9:g.35137171T>A	NCBI36
NG_007503.1:g.44253T>A , LRG_724:g.44253T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3257T>A MANE Select	ENSP00000269571.4:p.Phe1086Tyr
ENST00000269571.9:c.3257T>A	ENSP00000269571.4:p.Phe1086Tyr
ENST00000406381.6:c.3167T>A	ENSP00000385185.2:p.Phe1056Tyr
ENST00000445658.6:c.2429T>A	ENSP00000404047.2:p.Phe810Tyr
ENST00000541774.5:c.3212T>A	ENSP00000446466.1:p.Phe1071Tyr
ENST00000578373.5:c.*3047T>A	ENSP00000463427.1:n.*3047T>A
ENST00000584450.5:c.3160-297T>A	ENSP00000463714.1:n.3160-297T>A
ENST00000584601.5:c.3167T>A	ENSP00000462438.1:p.Phe1056Tyr
NM_001005862.2:c.3167T>A , LRG_724t1:c.3167T>A	NP_001005862.1:p.Phe1056Tyr
NM_001289936.1:c.3212T>A , LRG_724t4:c.3212T>A	NP_001276865.1:p.Phe1071Tyr
NM_001289937.1:c.3160-297T>A	NP_001276866.1:n.3160-297T>A
NM_004448.3:c.3257T>A , LRG_724t2:c.3257T>A	NP_004439.2:p.Phe1086Tyr
NR_110535.1:n.3581T>A
XM_024450641.1:c.3395T>A	XP_024306409.1:p.Phe1132Tyr
XM_024450642.1:c.3350T>A	XP_024306410.1:p.Phe1117Tyr
XM_024450643.1:c.3305T>A	XP_024306411.1:p.Phe1102Tyr
NM_001005862.3:c.3167T>A	NP_001005862.1:p.Phe1056Tyr
NM_001289936.2:c.3212T>A	NP_001276865.1:p.Phe1071Tyr
NM_001289937.2:c.3160-297T>A	NP_001276866.1:n.3160-297T>A
NM_001382782.1:c.3167T>A	NP_001369711.1:p.Phe1056Tyr
NM_001382783.1:c.3167T>A	NP_001369712.1:p.Phe1056Tyr
NM_001382784.1:c.3374T>A	NP_001369713.1:p.Phe1125Tyr
NM_001382785.1:c.3359T>A	NP_001369714.1:p.Phe1120Tyr
NM_001382786.1:c.3338T>A	NP_001369715.1:p.Phe1113Tyr
NM_001382787.1:c.3332T>A	NP_001369716.1:p.Phe1111Tyr
NM_001382788.1:c.3287T>A	NP_001369717.1:p.Phe1096Tyr
NM_001382789.1:c.3278T>A	NP_001369718.1:p.Phe1093Tyr
NM_001382790.1:c.3254T>A	NP_001369719.1:p.Phe1085Tyr
NM_001382791.1:c.3248T>A	NP_001369720.1:p.Phe1083Tyr
NM_001382792.1:c.3221T>A	NP_001369721.1:p.Phe1074Tyr
NM_001382793.1:c.3215T>A	NP_001369722.1:p.Phe1072Tyr
NM_001382794.1:c.3215T>A	NP_001369723.1:p.Phe1072Tyr
NM_001382795.1:c.3209T>A	NP_001369724.1:p.Phe1070Tyr
NM_001382796.1:c.3170T>A	NP_001369725.1:p.Phe1057Tyr
NM_001382797.1:c.3158T>A	NP_001369726.1:p.Phe1053Tyr
NM_001382798.1:c.3101T>A	NP_001369727.1:p.Phe1034Tyr
NM_001382799.1:c.3077T>A	NP_001369728.1:p.Phe1026Tyr
NM_001382800.1:c.3071T>A	NP_001369729.1:p.Phe1024Tyr
NM_001382801.1:c.3053T>A	NP_001369730.1:p.Phe1018Tyr
NM_001382802.1:c.2999T>A	NP_001369731.1:p.Phe1000Tyr
NM_001382803.1:c.3118-297T>A	NP_001369732.1:n.3118-297T>A
NM_001382804.1:c.2429T>A	NP_001369733.1:p.Phe810Tyr
NM_001382805.1:c.2306T>A	NP_001369734.1:p.Phe769Tyr
NM_001382806.1:c.2219T>A	NP_001369735.1:p.Phe740Tyr
NM_004448.4:c.3257T>A MANE Select	NP_004439.2:p.Phe1086Tyr
NR_110535.2:n.3495T>A