Canonical Allele Identifier: CA399281690

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37868183A>G (hg19) ; chr17:g.39711930A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39711930A>G , CM000679.2:g.39711930A>G	GRCh38
NC_000017.10:g.37868183A>G , CM000679.1:g.37868183A>G	GRCh37
NC_000017.9:g.35121709A>G	NCBI36
NG_007503.1:g.28791A>G , LRG_724:g.28791A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.904A>G MANE Select	ENSP00000269571.4:p.Asn302Asp
ENST00000269571.9:c.904A>G	ENSP00000269571.4:p.Asn302Asp
ENST00000406381.6:c.814A>G	ENSP00000385185.2:p.Asn272Asp
ENST00000445658.6:c.76A>G	ENSP00000404047.2:p.Asn26Asp
ENST00000541774.5:c.859A>G	ENSP00000446466.1:p.Asn287Asp
ENST00000578199.5:c.814A>G	ENSP00000462808.1:p.Asn272Asp
ENST00000578373.5:c.*694A>G	ENSP00000463427.1:n.*694A>G
ENST00000578502.1:c.129A>G
ENST00000582648.5:c.228A>G	ENSP00000462024.1:p.Thr76=
ENST00000582788.5:n.393A>G
ENST00000583038.5:n.1596A>G
ENST00000584450.5:c.904A>G	ENSP00000463714.1:p.Asn302Asp
ENST00000584601.5:c.814A>G	ENSP00000462438.1:p.Asn272Asp
ENST00000584908.5:n.916A>G
NM_001005862.2:c.814A>G , LRG_724t1:c.814A>G	NP_001005862.1:p.Asn272Asp
NM_001289936.1:c.859A>G , LRG_724t4:c.859A>G	NP_001276865.1:p.Asn287Asp
NM_001289937.1:c.904A>G	NP_001276866.1:p.Asn302Asp
NM_001289938.1:c.814A>G , LRG_724t3:c.814A>G	NP_001276867.1:p.Asn272Asp
NM_004448.3:c.904A>G , LRG_724t2:c.904A>G	NP_004439.2:p.Asn302Asp
NR_110535.1:n.1228A>G
XM_024450641.1:c.1042A>G	XP_024306409.1:p.Asn348Asp
XM_024450642.1:c.997A>G	XP_024306410.1:p.Asn333Asp
XM_024450643.1:c.952A>G	XP_024306411.1:p.Asn318Asp
NM_001005862.3:c.814A>G	NP_001005862.1:p.Asn272Asp
NM_001289936.2:c.859A>G	NP_001276865.1:p.Asn287Asp
NM_001289937.2:c.904A>G	NP_001276866.1:p.Asn302Asp
NM_001289938.2:c.814A>G	NP_001276867.1:p.Asn272Asp
NM_001382782.1:c.814A>G	NP_001369711.1:p.Asn272Asp
NM_001382783.1:c.814A>G	NP_001369712.1:p.Asn272Asp
NM_001382784.1:c.904A>G	NP_001369713.1:p.Asn302Asp
NM_001382785.1:c.904A>G	NP_001369714.1:p.Asn302Asp
NM_001382786.1:c.904A>G	NP_001369715.1:p.Asn302Asp
NM_001382787.1:c.979A>G	NP_001369716.1:p.Asn327Asp
NM_001382788.1:c.904A>G	NP_001369717.1:p.Asn302Asp
NM_001382789.1:c.904A>G	NP_001369718.1:p.Asn302Asp
NM_001382790.1:c.904A>G	NP_001369719.1:p.Asn302Asp
NM_001382791.1:c.895A>G	NP_001369720.1:p.Asn299Asp
NM_001382792.1:c.904A>G	NP_001369721.1:p.Asn302Asp
NM_001382793.1:c.904A>G	NP_001369722.1:p.Asn302Asp
NM_001382794.1:c.904A>G	NP_001369723.1:p.Asn302Asp
NM_001382795.1:c.904A>G	NP_001369724.1:p.Asn302Asp
NM_001382796.1:c.904A>G	NP_001369725.1:p.Asn302Asp
NM_001382797.1:c.904A>G	NP_001369726.1:p.Asn302Asp
NM_001382798.1:c.904A>G	NP_001369727.1:p.Asn302Asp
NM_001382799.1:c.724A>G	NP_001369728.1:p.Asn242Asp
NM_001382800.1:c.904A>G	NP_001369729.1:p.Asn302Asp
NM_001382801.1:c.904A>G	NP_001369730.1:p.Asn302Asp
NM_001382802.1:c.646A>G	NP_001369731.1:p.Asn216Asp
NM_001382803.1:c.904A>G	NP_001369732.1:p.Asn302Asp
NM_001382804.1:c.76A>G	NP_001369733.1:p.Asn26Asp
NM_001382805.1:c.904A>G	NP_001369734.1:p.Asn302Asp
NM_001382806.1:c.904A>G	NP_001369735.1:p.Asn302Asp
NM_004448.4:c.904A>G MANE Select	NP_004439.2:p.Asn302Asp
NR_110535.2:n.1142A>G