Canonical Allele Identifier: CA399304074

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145862098
• MyVariant Identifiers: chr17:g.37881305A>G (hg19) ; chr17:g.39725052A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725052A>G , CM000679.2:g.39725052A>G	GRCh38
NC_000017.10:g.37881305A>G , CM000679.1:g.37881305A>G	GRCh37
NC_000017.9:g.35134831A>G	NCBI36
NG_007503.1:g.41913A>G , LRG_724:g.41913A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2497A>G MANE Select	ENSP00000269571.4:p.Met833Val
ENST00000269571.9:c.2497A>G	ENSP00000269571.4:p.Met833Val
ENST00000406381.6:c.2407A>G	ENSP00000385185.2:p.Met803Val
ENST00000445658.6:c.1669A>G	ENSP00000404047.2:p.Met557Val
ENST00000541774.5:c.2452A>G	ENSP00000446466.1:p.Met818Val
ENST00000578373.5:c.*2287A>G	ENSP00000463427.1:n.*2287A>G
ENST00000580074.1:c.603A>G
ENST00000583038.5:n.3631A>G
ENST00000584450.5:c.2497A>G	ENSP00000463714.1:p.Met833Val
ENST00000584601.5:c.2407A>G	ENSP00000462438.1:p.Met803Val
NM_001005862.2:c.2407A>G , LRG_724t1:c.2407A>G	NP_001005862.1:p.Met803Val
NM_001289936.1:c.2452A>G , LRG_724t4:c.2452A>G	NP_001276865.1:p.Met818Val
NM_001289937.1:c.2497A>G	NP_001276866.1:p.Met833Val
NM_004448.3:c.2497A>G , LRG_724t2:c.2497A>G	NP_004439.2:p.Met833Val
NR_110535.1:n.2821A>G
XM_024450641.1:c.2635A>G	XP_024306409.1:p.Met879Val
XM_024450642.1:c.2590A>G	XP_024306410.1:p.Met864Val
XM_024450643.1:c.2545A>G	XP_024306411.1:p.Met849Val
NM_001005862.3:c.2407A>G	NP_001005862.1:p.Met803Val
NM_001289936.2:c.2452A>G	NP_001276865.1:p.Met818Val
NM_001289937.2:c.2497A>G	NP_001276866.1:p.Met833Val
NM_001382782.1:c.2407A>G	NP_001369711.1:p.Met803Val
NM_001382783.1:c.2407A>G	NP_001369712.1:p.Met803Val
NM_001382784.1:c.2614A>G	NP_001369713.1:p.Met872Val
NM_001382785.1:c.2599A>G	NP_001369714.1:p.Met867Val
NM_001382786.1:c.2578A>G	NP_001369715.1:p.Met860Val
NM_001382787.1:c.2572A>G	NP_001369716.1:p.Met858Val
NM_001382788.1:c.2527A>G	NP_001369717.1:p.Met843Val
NM_001382789.1:c.2518A>G	NP_001369718.1:p.Met840Val
NM_001382790.1:c.2494A>G	NP_001369719.1:p.Met832Val
NM_001382791.1:c.2488A>G	NP_001369720.1:p.Met830Val
NM_001382792.1:c.2461A>G	NP_001369721.1:p.Met821Val
NM_001382793.1:c.2455A>G	NP_001369722.1:p.Met819Val
NM_001382794.1:c.2455A>G	NP_001369723.1:p.Met819Val
NM_001382795.1:c.2449A>G	NP_001369724.1:p.Met817Val
NM_001382796.1:c.2497A>G	NP_001369725.1:p.Met833Val
NM_001382797.1:c.2398A>G	NP_001369726.1:p.Met800Val
NM_001382798.1:c.2493+141A>G	NP_001369727.1:n.2493+141A>G
NM_001382799.1:c.2317A>G	NP_001369728.1:p.Met773Val
NM_001382800.1:c.2311A>G	NP_001369729.1:p.Met771Val
NM_001382801.1:c.2445+141A>G	NP_001369730.1:n.2445+141A>G
NM_001382802.1:c.2239A>G	NP_001369731.1:p.Met747Val
NM_001382803.1:c.2455A>G	NP_001369732.1:p.Met819Val
NM_001382804.1:c.1669A>G	NP_001369733.1:p.Met557Val
NM_001382805.1:c.2208+1392A>G	NP_001369734.1:n.2208+1392A>G
NM_001382806.1:c.1459A>G	NP_001369735.1:p.Met487Val
NM_004448.4:c.2497A>G MANE Select	NP_004439.2:p.Met833Val
NR_110535.2:n.2735A>G