Canonical Allele Identifier: CA399304211

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145862829
• MyVariant Identifiers: chr17:g.37881322T>A (hg19) ; chr17:g.39725069T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725069T>A , CM000679.2:g.39725069T>A	GRCh38
NC_000017.10:g.37881322T>A , CM000679.1:g.37881322T>A	GRCh37
NC_000017.9:g.35134848T>A	NCBI36
NG_007503.1:g.41930T>A , LRG_724:g.41930T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2514T>A MANE Select	ENSP00000269571.4:p.Asp838Glu
ENST00000269571.9:c.2514T>A	ENSP00000269571.4:p.Asp838Glu
ENST00000406381.6:c.2424T>A	ENSP00000385185.2:p.Asp808Glu
ENST00000445658.6:c.1686T>A	ENSP00000404047.2:p.Asp562Glu
ENST00000541774.5:c.2469T>A	ENSP00000446466.1:p.Asp823Glu
ENST00000578373.5:c.*2304T>A	ENSP00000463427.1:n.*2304T>A
ENST00000580074.1:c.620T>A
ENST00000583038.5:n.3648T>A
ENST00000584450.5:c.2514T>A	ENSP00000463714.1:p.Asp838Glu
ENST00000584601.5:c.2424T>A	ENSP00000462438.1:p.Asp808Glu
NM_001005862.2:c.2424T>A , LRG_724t1:c.2424T>A	NP_001005862.1:p.Asp808Glu
NM_001289936.1:c.2469T>A , LRG_724t4:c.2469T>A	NP_001276865.1:p.Asp823Glu
NM_001289937.1:c.2514T>A	NP_001276866.1:p.Asp838Glu
NM_004448.3:c.2514T>A , LRG_724t2:c.2514T>A	NP_004439.2:p.Asp838Glu
NR_110535.1:n.2838T>A
XM_024450641.1:c.2652T>A	XP_024306409.1:p.Asp884Glu
XM_024450642.1:c.2607T>A	XP_024306410.1:p.Asp869Glu
XM_024450643.1:c.2562T>A	XP_024306411.1:p.Asp854Glu
NM_001005862.3:c.2424T>A	NP_001005862.1:p.Asp808Glu
NM_001289936.2:c.2469T>A	NP_001276865.1:p.Asp823Glu
NM_001289937.2:c.2514T>A	NP_001276866.1:p.Asp838Glu
NM_001382782.1:c.2424T>A	NP_001369711.1:p.Asp808Glu
NM_001382783.1:c.2424T>A	NP_001369712.1:p.Asp808Glu
NM_001382784.1:c.2631T>A	NP_001369713.1:p.Asp877Glu
NM_001382785.1:c.2616T>A	NP_001369714.1:p.Asp872Glu
NM_001382786.1:c.2595T>A	NP_001369715.1:p.Asp865Glu
NM_001382787.1:c.2589T>A	NP_001369716.1:p.Asp863Glu
NM_001382788.1:c.2544T>A	NP_001369717.1:p.Asp848Glu
NM_001382789.1:c.2535T>A	NP_001369718.1:p.Asp845Glu
NM_001382790.1:c.2511T>A	NP_001369719.1:p.Asp837Glu
NM_001382791.1:c.2505T>A	NP_001369720.1:p.Asp835Glu
NM_001382792.1:c.2478T>A	NP_001369721.1:p.Asp826Glu
NM_001382793.1:c.2472T>A	NP_001369722.1:p.Asp824Glu
NM_001382794.1:c.2472T>A	NP_001369723.1:p.Asp824Glu
NM_001382795.1:c.2466T>A	NP_001369724.1:p.Asp822Glu
NM_001382796.1:c.2514T>A	NP_001369725.1:p.Asp838Glu
NM_001382797.1:c.2415T>A	NP_001369726.1:p.Asp805Glu
NM_001382798.1:c.2493+158T>A	NP_001369727.1:n.2493+158T>A
NM_001382799.1:c.2334T>A	NP_001369728.1:p.Asp778Glu
NM_001382800.1:c.2328T>A	NP_001369729.1:p.Asp776Glu
NM_001382801.1:c.2445+158T>A	NP_001369730.1:n.2445+158T>A
NM_001382802.1:c.2256T>A	NP_001369731.1:p.Asp752Glu
NM_001382803.1:c.2472T>A	NP_001369732.1:p.Asp824Glu
NM_001382804.1:c.1686T>A	NP_001369733.1:p.Asp562Glu
NM_001382805.1:c.2208+1409T>A	NP_001369734.1:n.2208+1409T>A
NM_001382806.1:c.1476T>A	NP_001369735.1:p.Asp492Glu
NM_004448.4:c.2514T>A MANE Select	NP_004439.2:p.Asp838Glu
NR_110535.2:n.2752T>A