Canonical Allele Identifier: CA399303448

Gene: ERBB2

Linked Data

• dbSNP Id: rs1398689580
• MyVariant Identifiers: chr17:g.37881098T>A (hg19) ; chr17:g.39724845T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724845T>A , CM000679.2:g.39724845T>A	GRCh38
NC_000017.10:g.37881098T>A , CM000679.1:g.37881098T>A	GRCh37
NC_000017.9:g.35134624T>A	NCBI36
NG_007503.1:g.41706T>A , LRG_724:g.41706T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2427T>A MANE Select	ENSP00000269571.4:p.His809Gln
ENST00000269571.9:c.2427T>A	ENSP00000269571.4:p.His809Gln
ENST00000406381.6:c.2337T>A	ENSP00000385185.2:p.His779Gln
ENST00000445658.6:c.1599T>A	ENSP00000404047.2:p.His533Gln
ENST00000541774.5:c.2382T>A	ENSP00000446466.1:p.His794Gln
ENST00000578373.5:c.*2217T>A	ENSP00000463427.1:n.*2217T>A
ENST00000580074.1:c.533T>A
ENST00000583038.5:n.3561T>A
ENST00000584450.5:c.2427T>A	ENSP00000463714.1:p.His809Gln
ENST00000584601.5:c.2337T>A	ENSP00000462438.1:p.His779Gln
NM_001005862.2:c.2337T>A , LRG_724t1:c.2337T>A	NP_001005862.1:p.His779Gln
NM_001289936.1:c.2382T>A , LRG_724t4:c.2382T>A	NP_001276865.1:p.His794Gln
NM_001289937.1:c.2427T>A	NP_001276866.1:p.His809Gln
NM_004448.3:c.2427T>A , LRG_724t2:c.2427T>A	NP_004439.2:p.His809Gln
NR_110535.1:n.2751T>A
XM_024450641.1:c.2565T>A	XP_024306409.1:p.His855Gln
XM_024450642.1:c.2520T>A	XP_024306410.1:p.His840Gln
XM_024450643.1:c.2475T>A	XP_024306411.1:p.His825Gln
NM_001005862.3:c.2337T>A	NP_001005862.1:p.His779Gln
NM_001289936.2:c.2382T>A	NP_001276865.1:p.His794Gln
NM_001289937.2:c.2427T>A	NP_001276866.1:p.His809Gln
NM_001382782.1:c.2337T>A	NP_001369711.1:p.His779Gln
NM_001382783.1:c.2337T>A	NP_001369712.1:p.His779Gln
NM_001382784.1:c.2544T>A	NP_001369713.1:p.His848Gln
NM_001382785.1:c.2529T>A	NP_001369714.1:p.His843Gln
NM_001382786.1:c.2508T>A	NP_001369715.1:p.His836Gln
NM_001382787.1:c.2502T>A	NP_001369716.1:p.His834Gln
NM_001382788.1:c.2457T>A	NP_001369717.1:p.His819Gln
NM_001382789.1:c.2448T>A	NP_001369718.1:p.His816Gln
NM_001382790.1:c.2424T>A	NP_001369719.1:p.His808Gln
NM_001382791.1:c.2418T>A	NP_001369720.1:p.His806Gln
NM_001382792.1:c.2391T>A	NP_001369721.1:p.His797Gln
NM_001382793.1:c.2385T>A	NP_001369722.1:p.His795Gln
NM_001382794.1:c.2385T>A	NP_001369723.1:p.His795Gln
NM_001382795.1:c.2379T>A	NP_001369724.1:p.His793Gln
NM_001382796.1:c.2427T>A	NP_001369725.1:p.His809Gln
NM_001382797.1:c.2328T>A	NP_001369726.1:p.His776Gln
NM_001382798.1:c.2427T>A	NP_001369727.1:p.His809Gln
NM_001382799.1:c.2247T>A	NP_001369728.1:p.His749Gln
NM_001382800.1:c.2308-204T>A	NP_001369729.1:n.2308-204T>A
NM_001382801.1:c.2379T>A	NP_001369730.1:p.His793Gln
NM_001382802.1:c.2169T>A	NP_001369731.1:p.His723Gln
NM_001382803.1:c.2385T>A	NP_001369732.1:p.His795Gln
NM_001382804.1:c.1599T>A	NP_001369733.1:p.His533Gln
NM_001382805.1:c.2208+1185T>A	NP_001369734.1:n.2208+1185T>A
NM_001382806.1:c.1389T>A	NP_001369735.1:p.His463Gln
NM_004448.4:c.2427T>A MANE Select	NP_004439.2:p.His809Gln
NR_110535.2:n.2665T>A