Canonical Allele Identifier: CA399304336

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145863486
• MyVariant Identifiers: chr17:g.37881338A>T (hg19) ; chr17:g.39725085A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725085A>T , CM000679.2:g.39725085A>T	GRCh38
NC_000017.10:g.37881338A>T , CM000679.1:g.37881338A>T	GRCh37
NC_000017.9:g.35134864A>T	NCBI36
NG_007503.1:g.41946A>T , LRG_724:g.41946A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2530A>T MANE Select	ENSP00000269571.4:p.Arg844Trp
ENST00000269571.9:c.2530A>T	ENSP00000269571.4:p.Arg844Trp
ENST00000406381.6:c.2440A>T	ENSP00000385185.2:p.Arg814Trp
ENST00000445658.6:c.1702A>T	ENSP00000404047.2:p.Arg568Trp
ENST00000541774.5:c.2485A>T	ENSP00000446466.1:p.Arg829Trp
ENST00000578373.5:c.*2320A>T	ENSP00000463427.1:n.*2320A>T
ENST00000580074.1:c.636A>T
ENST00000583038.5:n.3664A>T
ENST00000584450.5:c.2530A>T	ENSP00000463714.1:p.Arg844Trp
ENST00000584601.5:c.2440A>T	ENSP00000462438.1:p.Arg814Trp
NM_001005862.2:c.2440A>T , LRG_724t1:c.2440A>T	NP_001005862.1:p.Arg814Trp
NM_001289936.1:c.2485A>T , LRG_724t4:c.2485A>T	NP_001276865.1:p.Arg829Trp
NM_001289937.1:c.2530A>T	NP_001276866.1:p.Arg844Trp
NM_004448.3:c.2530A>T , LRG_724t2:c.2530A>T	NP_004439.2:p.Arg844Trp
NR_110535.1:n.2854A>T
XM_024450641.1:c.2668A>T	XP_024306409.1:p.Arg890Trp
XM_024450642.1:c.2623A>T	XP_024306410.1:p.Arg875Trp
XM_024450643.1:c.2578A>T	XP_024306411.1:p.Arg860Trp
NM_001005862.3:c.2440A>T	NP_001005862.1:p.Arg814Trp
NM_001289936.2:c.2485A>T	NP_001276865.1:p.Arg829Trp
NM_001289937.2:c.2530A>T	NP_001276866.1:p.Arg844Trp
NM_001382782.1:c.2440A>T	NP_001369711.1:p.Arg814Trp
NM_001382783.1:c.2440A>T	NP_001369712.1:p.Arg814Trp
NM_001382784.1:c.2647A>T	NP_001369713.1:p.Arg883Trp
NM_001382785.1:c.2632A>T	NP_001369714.1:p.Arg878Trp
NM_001382786.1:c.2611A>T	NP_001369715.1:p.Arg871Trp
NM_001382787.1:c.2605A>T	NP_001369716.1:p.Arg869Trp
NM_001382788.1:c.2560A>T	NP_001369717.1:p.Arg854Trp
NM_001382789.1:c.2551A>T	NP_001369718.1:p.Arg851Trp
NM_001382790.1:c.2527A>T	NP_001369719.1:p.Arg843Trp
NM_001382791.1:c.2521A>T	NP_001369720.1:p.Arg841Trp
NM_001382792.1:c.2494A>T	NP_001369721.1:p.Arg832Trp
NM_001382793.1:c.2488A>T	NP_001369722.1:p.Arg830Trp
NM_001382794.1:c.2488A>T	NP_001369723.1:p.Arg830Trp
NM_001382795.1:c.2482A>T	NP_001369724.1:p.Arg828Trp
NM_001382796.1:c.2530A>T	NP_001369725.1:p.Arg844Trp
NM_001382797.1:c.2431A>T	NP_001369726.1:p.Arg811Trp
NM_001382798.1:c.2493+174A>T	NP_001369727.1:n.2493+174A>T
NM_001382799.1:c.2350A>T	NP_001369728.1:p.Arg784Trp
NM_001382800.1:c.2344A>T	NP_001369729.1:p.Arg782Trp
NM_001382801.1:c.2445+174A>T	NP_001369730.1:n.2445+174A>T
NM_001382802.1:c.2272A>T	NP_001369731.1:p.Arg758Trp
NM_001382803.1:c.2488A>T	NP_001369732.1:p.Arg830Trp
NM_001382804.1:c.1702A>T	NP_001369733.1:p.Arg568Trp
NM_001382805.1:c.2208+1425A>T	NP_001369734.1:n.2208+1425A>T
NM_001382806.1:c.1492A>T	NP_001369735.1:p.Arg498Trp
NM_004448.4:c.2530A>T MANE Select	NP_004439.2:p.Arg844Trp
NR_110535.2:n.2768A>T