Canonical Allele Identifier: CA399304320

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881336A>G (hg19) ; chr17:g.39725083A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725083A>G , CM000679.2:g.39725083A>G	GRCh38
NC_000017.10:g.37881336A>G , CM000679.1:g.37881336A>G	GRCh37
NC_000017.9:g.35134862A>G	NCBI36
NG_007503.1:g.41944A>G , LRG_724:g.41944A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2528A>G MANE Select	ENSP00000269571.4:p.His843Arg
ENST00000269571.9:c.2528A>G	ENSP00000269571.4:p.His843Arg
ENST00000406381.6:c.2438A>G	ENSP00000385185.2:p.His813Arg
ENST00000445658.6:c.1700A>G	ENSP00000404047.2:p.His567Arg
ENST00000541774.5:c.2483A>G	ENSP00000446466.1:p.His828Arg
ENST00000578373.5:c.*2318A>G	ENSP00000463427.1:n.*2318A>G
ENST00000580074.1:c.634A>G
ENST00000583038.5:n.3662A>G
ENST00000584450.5:c.2528A>G	ENSP00000463714.1:p.His843Arg
ENST00000584601.5:c.2438A>G	ENSP00000462438.1:p.His813Arg
NM_001005862.2:c.2438A>G , LRG_724t1:c.2438A>G	NP_001005862.1:p.His813Arg
NM_001289936.1:c.2483A>G , LRG_724t4:c.2483A>G	NP_001276865.1:p.His828Arg
NM_001289937.1:c.2528A>G	NP_001276866.1:p.His843Arg
NM_004448.3:c.2528A>G , LRG_724t2:c.2528A>G	NP_004439.2:p.His843Arg
NR_110535.1:n.2852A>G
XM_024450641.1:c.2666A>G	XP_024306409.1:p.His889Arg
XM_024450642.1:c.2621A>G	XP_024306410.1:p.His874Arg
XM_024450643.1:c.2576A>G	XP_024306411.1:p.His859Arg
NM_001005862.3:c.2438A>G	NP_001005862.1:p.His813Arg
NM_001289936.2:c.2483A>G	NP_001276865.1:p.His828Arg
NM_001289937.2:c.2528A>G	NP_001276866.1:p.His843Arg
NM_001382782.1:c.2438A>G	NP_001369711.1:p.His813Arg
NM_001382783.1:c.2438A>G	NP_001369712.1:p.His813Arg
NM_001382784.1:c.2645A>G	NP_001369713.1:p.His882Arg
NM_001382785.1:c.2630A>G	NP_001369714.1:p.His877Arg
NM_001382786.1:c.2609A>G	NP_001369715.1:p.His870Arg
NM_001382787.1:c.2603A>G	NP_001369716.1:p.His868Arg
NM_001382788.1:c.2558A>G	NP_001369717.1:p.His853Arg
NM_001382789.1:c.2549A>G	NP_001369718.1:p.His850Arg
NM_001382790.1:c.2525A>G	NP_001369719.1:p.His842Arg
NM_001382791.1:c.2519A>G	NP_001369720.1:p.His840Arg
NM_001382792.1:c.2492A>G	NP_001369721.1:p.His831Arg
NM_001382793.1:c.2486A>G	NP_001369722.1:p.His829Arg
NM_001382794.1:c.2486A>G	NP_001369723.1:p.His829Arg
NM_001382795.1:c.2480A>G	NP_001369724.1:p.His827Arg
NM_001382796.1:c.2528A>G	NP_001369725.1:p.His843Arg
NM_001382797.1:c.2429A>G	NP_001369726.1:p.His810Arg
NM_001382798.1:c.2493+172A>G	NP_001369727.1:n.2493+172A>G
NM_001382799.1:c.2348A>G	NP_001369728.1:p.His783Arg
NM_001382800.1:c.2342A>G	NP_001369729.1:p.His781Arg
NM_001382801.1:c.2445+172A>G	NP_001369730.1:n.2445+172A>G
NM_001382802.1:c.2270A>G	NP_001369731.1:p.His757Arg
NM_001382803.1:c.2486A>G	NP_001369732.1:p.His829Arg
NM_001382804.1:c.1700A>G	NP_001369733.1:p.His567Arg
NM_001382805.1:c.2208+1423A>G	NP_001369734.1:n.2208+1423A>G
NM_001382806.1:c.1490A>G	NP_001369735.1:p.His497Arg
NM_004448.4:c.2528A>G MANE Select	NP_004439.2:p.His843Arg
NR_110535.2:n.2766A>G