Canonical Allele Identifier: CA399304653

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881381A>G (hg19) ; chr17:g.39725128A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725128A>G , CM000679.2:g.39725128A>G	GRCh38
NC_000017.10:g.37881381A>G , CM000679.1:g.37881381A>G	GRCh37
NC_000017.9:g.35134907A>G	NCBI36
NG_007503.1:g.41989A>G , LRG_724:g.41989A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2573A>G MANE Select	ENSP00000269571.4:p.His858Arg
ENST00000269571.9:c.2573A>G	ENSP00000269571.4:p.His858Arg
ENST00000406381.6:c.2483A>G	ENSP00000385185.2:p.His828Arg
ENST00000445658.6:c.1745A>G	ENSP00000404047.2:p.His582Arg
ENST00000541774.5:c.2528A>G	ENSP00000446466.1:p.His843Arg
ENST00000578373.5:c.*2363A>G	ENSP00000463427.1:n.*2363A>G
ENST00000580074.1:c.679A>G
ENST00000583038.5:n.3707A>G
ENST00000584450.5:c.2573A>G	ENSP00000463714.1:p.His858Arg
ENST00000584601.5:c.2483A>G	ENSP00000462438.1:p.His828Arg
NM_001005862.2:c.2483A>G , LRG_724t1:c.2483A>G	NP_001005862.1:p.His828Arg
NM_001289936.1:c.2528A>G , LRG_724t4:c.2528A>G	NP_001276865.1:p.His843Arg
NM_001289937.1:c.2573A>G	NP_001276866.1:p.His858Arg
NM_004448.3:c.2573A>G , LRG_724t2:c.2573A>G	NP_004439.2:p.His858Arg
NR_110535.1:n.2897A>G
XM_024450641.1:c.2711A>G	XP_024306409.1:p.His904Arg
XM_024450642.1:c.2666A>G	XP_024306410.1:p.His889Arg
XM_024450643.1:c.2621A>G	XP_024306411.1:p.His874Arg
NM_001005862.3:c.2483A>G	NP_001005862.1:p.His828Arg
NM_001289936.2:c.2528A>G	NP_001276865.1:p.His843Arg
NM_001289937.2:c.2573A>G	NP_001276866.1:p.His858Arg
NM_001382782.1:c.2483A>G	NP_001369711.1:p.His828Arg
NM_001382783.1:c.2483A>G	NP_001369712.1:p.His828Arg
NM_001382784.1:c.2690A>G	NP_001369713.1:p.His897Arg
NM_001382785.1:c.2675A>G	NP_001369714.1:p.His892Arg
NM_001382786.1:c.2654A>G	NP_001369715.1:p.His885Arg
NM_001382787.1:c.2648A>G	NP_001369716.1:p.His883Arg
NM_001382788.1:c.2603A>G	NP_001369717.1:p.His868Arg
NM_001382789.1:c.2594A>G	NP_001369718.1:p.His865Arg
NM_001382790.1:c.2570A>G	NP_001369719.1:p.His857Arg
NM_001382791.1:c.2564A>G	NP_001369720.1:p.His855Arg
NM_001382792.1:c.2537A>G	NP_001369721.1:p.His846Arg
NM_001382793.1:c.2531A>G	NP_001369722.1:p.His844Arg
NM_001382794.1:c.2531A>G	NP_001369723.1:p.His844Arg
NM_001382795.1:c.2525A>G	NP_001369724.1:p.His842Arg
NM_001382796.1:c.2573A>G	NP_001369725.1:p.His858Arg
NM_001382797.1:c.2474A>G	NP_001369726.1:p.His825Arg
NM_001382798.1:c.2494-199A>G	NP_001369727.1:n.2494-199A>G
NM_001382799.1:c.2393A>G	NP_001369728.1:p.His798Arg
NM_001382800.1:c.2387A>G	NP_001369729.1:p.His796Arg
NM_001382801.1:c.2446-199A>G	NP_001369730.1:n.2446-199A>G
NM_001382802.1:c.2315A>G	NP_001369731.1:p.His772Arg
NM_001382803.1:c.2531A>G	NP_001369732.1:p.His844Arg
NM_001382804.1:c.1745A>G	NP_001369733.1:p.His582Arg
NM_001382805.1:c.2208+1468A>G	NP_001369734.1:n.2208+1468A>G
NM_001382806.1:c.1535A>G	NP_001369735.1:p.His512Arg
NM_004448.4:c.2573A>G MANE Select	NP_004439.2:p.His858Arg
NR_110535.2:n.2811A>G