Canonical Allele Identifier: CA399313717

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143304048
• MyVariant Identifiers: chr17:g.37884106A>G (hg19) ; chr17:g.39727853A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727853A>G , CM000679.2:g.39727853A>G	GRCh38
NC_000017.10:g.37884106A>G , CM000679.1:g.37884106A>G	GRCh37
NC_000017.9:g.35137632A>G	NCBI36
NG_007503.1:g.44714A>G , LRG_724:g.44714A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3577A>G MANE Select	ENSP00000269571.4:p.Asn1193Asp
ENST00000269571.9:c.3577A>G	ENSP00000269571.4:p.Asn1193Asp
ENST00000406381.6:c.3487A>G	ENSP00000385185.2:p.Asn1163Asp
ENST00000445658.6:c.2749A>G	ENSP00000404047.2:p.Asn917Asp
ENST00000541774.5:c.3532A>G	ENSP00000446466.1:p.Asn1178Asp
ENST00000578373.5:c.*3367A>G	ENSP00000463427.1:n.*3367A>G
ENST00000584450.5:c.*156A>G	ENSP00000463714.1:n.*156A>G
ENST00000584601.5:c.3487A>G	ENSP00000462438.1:p.Asn1163Asp
NM_001005862.2:c.3487A>G , LRG_724t1:c.3487A>G	NP_001005862.1:p.Asn1163Asp
NM_001289936.1:c.3532A>G , LRG_724t4:c.3532A>G	NP_001276865.1:p.Asn1178Asp
NM_001289937.1:c.*156A>G	NP_001276866.1:n.*156A>G
NM_004448.3:c.3577A>G , LRG_724t2:c.3577A>G	NP_004439.2:p.Asn1193Asp
NR_110535.1:n.3901A>G
XM_024450641.1:c.3715A>G	XP_024306409.1:p.Asn1239Asp
XM_024450642.1:c.3670A>G	XP_024306410.1:p.Asn1224Asp
XM_024450643.1:c.3625A>G	XP_024306411.1:p.Asn1209Asp
NM_001005862.3:c.3487A>G	NP_001005862.1:p.Asn1163Asp
NM_001289936.2:c.3532A>G	NP_001276865.1:p.Asn1178Asp
NM_001289937.2:c.*156A>G	NP_001276866.1:n.*156A>G
NM_001382782.1:c.3487A>G	NP_001369711.1:p.Asn1163Asp
NM_001382783.1:c.3487A>G	NP_001369712.1:p.Asn1163Asp
NM_001382784.1:c.3694A>G	NP_001369713.1:p.Asn1232Asp
NM_001382785.1:c.3679A>G	NP_001369714.1:p.Asn1227Asp
NM_001382786.1:c.3658A>G	NP_001369715.1:p.Asn1220Asp
NM_001382787.1:c.3652A>G	NP_001369716.1:p.Asn1218Asp
NM_001382788.1:c.3607A>G	NP_001369717.1:p.Asn1203Asp
NM_001382789.1:c.3598A>G	NP_001369718.1:p.Asn1200Asp
NM_001382790.1:c.3574A>G	NP_001369719.1:p.Asn1192Asp
NM_001382791.1:c.3568A>G	NP_001369720.1:p.Asn1190Asp
NM_001382792.1:c.3541A>G	NP_001369721.1:p.Asn1181Asp
NM_001382793.1:c.3535A>G	NP_001369722.1:p.Asn1179Asp
NM_001382794.1:c.3535A>G	NP_001369723.1:p.Asn1179Asp
NM_001382795.1:c.3529A>G	NP_001369724.1:p.Asn1177Asp
NM_001382796.1:c.3490A>G	NP_001369725.1:p.Asn1164Asp
NM_001382797.1:c.3478A>G	NP_001369726.1:p.Asn1160Asp
NM_001382798.1:c.3421A>G	NP_001369727.1:p.Asn1141Asp
NM_001382799.1:c.3397A>G	NP_001369728.1:p.Asn1133Asp
NM_001382800.1:c.3391A>G	NP_001369729.1:p.Asn1131Asp
NM_001382801.1:c.3373A>G	NP_001369730.1:p.Asn1125Asp
NM_001382802.1:c.3319A>G	NP_001369731.1:p.Asn1107Asp
NM_001382803.1:c.*156A>G	NP_001369732.1:n.*156A>G
NM_001382804.1:c.2749A>G	NP_001369733.1:p.Asn917Asp
NM_001382805.1:c.2626A>G	NP_001369734.1:p.Asn876Asp
NM_001382806.1:c.2539A>G	NP_001369735.1:p.Asn847Asp
NM_004448.4:c.3577A>G MANE Select	NP_004439.2:p.Asn1193Asp
NR_110535.2:n.3815A>G