Canonical Allele Identifier: CA399304528

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145864656
• MyVariant Identifiers: chr17:g.37881366T>A (hg19) ; chr17:g.39725113T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725113T>A , CM000679.2:g.39725113T>A	GRCh38
NC_000017.10:g.37881366T>A , CM000679.1:g.37881366T>A	GRCh37
NC_000017.9:g.35134892T>A	NCBI36
NG_007503.1:g.41974T>A , LRG_724:g.41974T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2558T>A MANE Select	ENSP00000269571.4:p.Val853Asp
ENST00000269571.9:c.2558T>A	ENSP00000269571.4:p.Val853Asp
ENST00000406381.6:c.2468T>A	ENSP00000385185.2:p.Val823Asp
ENST00000445658.6:c.1730T>A	ENSP00000404047.2:p.Val577Asp
ENST00000541774.5:c.2513T>A	ENSP00000446466.1:p.Val838Asp
ENST00000578373.5:c.*2348T>A	ENSP00000463427.1:n.*2348T>A
ENST00000580074.1:c.664T>A
ENST00000583038.5:n.3692T>A
ENST00000584450.5:c.2558T>A	ENSP00000463714.1:p.Val853Asp
ENST00000584601.5:c.2468T>A	ENSP00000462438.1:p.Val823Asp
NM_001005862.2:c.2468T>A , LRG_724t1:c.2468T>A	NP_001005862.1:p.Val823Asp
NM_001289936.1:c.2513T>A , LRG_724t4:c.2513T>A	NP_001276865.1:p.Val838Asp
NM_001289937.1:c.2558T>A	NP_001276866.1:p.Val853Asp
NM_004448.3:c.2558T>A , LRG_724t2:c.2558T>A	NP_004439.2:p.Val853Asp
NR_110535.1:n.2882T>A
XM_024450641.1:c.2696T>A	XP_024306409.1:p.Val899Asp
XM_024450642.1:c.2651T>A	XP_024306410.1:p.Val884Asp
XM_024450643.1:c.2606T>A	XP_024306411.1:p.Val869Asp
NM_001005862.3:c.2468T>A	NP_001005862.1:p.Val823Asp
NM_001289936.2:c.2513T>A	NP_001276865.1:p.Val838Asp
NM_001289937.2:c.2558T>A	NP_001276866.1:p.Val853Asp
NM_001382782.1:c.2468T>A	NP_001369711.1:p.Val823Asp
NM_001382783.1:c.2468T>A	NP_001369712.1:p.Val823Asp
NM_001382784.1:c.2675T>A	NP_001369713.1:p.Val892Asp
NM_001382785.1:c.2660T>A	NP_001369714.1:p.Val887Asp
NM_001382786.1:c.2639T>A	NP_001369715.1:p.Val880Asp
NM_001382787.1:c.2633T>A	NP_001369716.1:p.Val878Asp
NM_001382788.1:c.2588T>A	NP_001369717.1:p.Val863Asp
NM_001382789.1:c.2579T>A	NP_001369718.1:p.Val860Asp
NM_001382790.1:c.2555T>A	NP_001369719.1:p.Val852Asp
NM_001382791.1:c.2549T>A	NP_001369720.1:p.Val850Asp
NM_001382792.1:c.2522T>A	NP_001369721.1:p.Val841Asp
NM_001382793.1:c.2516T>A	NP_001369722.1:p.Val839Asp
NM_001382794.1:c.2516T>A	NP_001369723.1:p.Val839Asp
NM_001382795.1:c.2510T>A	NP_001369724.1:p.Val837Asp
NM_001382796.1:c.2558T>A	NP_001369725.1:p.Val853Asp
NM_001382797.1:c.2459T>A	NP_001369726.1:p.Val820Asp
NM_001382798.1:c.2493+202T>A	NP_001369727.1:n.2493+202T>A
NM_001382799.1:c.2378T>A	NP_001369728.1:p.Val793Asp
NM_001382800.1:c.2372T>A	NP_001369729.1:p.Val791Asp
NM_001382801.1:c.2445+202T>A	NP_001369730.1:n.2445+202T>A
NM_001382802.1:c.2300T>A	NP_001369731.1:p.Val767Asp
NM_001382803.1:c.2516T>A	NP_001369732.1:p.Val839Asp
NM_001382804.1:c.1730T>A	NP_001369733.1:p.Val577Asp
NM_001382805.1:c.2208+1453T>A	NP_001369734.1:n.2208+1453T>A
NM_001382806.1:c.1520T>A	NP_001369735.1:p.Val507Asp
NM_004448.4:c.2558T>A MANE Select	NP_004439.2:p.Val853Asp
NR_110535.2:n.2796T>A