Canonical Allele Identifier: CA399304664

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39725129-T-G
• MyVariant Identifiers: chr17:g.37881382T>G (hg19) ; chr17:g.39725129T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725129T>G , CM000679.2:g.39725129T>G	GRCh38
NC_000017.10:g.37881382T>G , CM000679.1:g.37881382T>G	GRCh37
NC_000017.9:g.35134908T>G	NCBI36
NG_007503.1:g.41990T>G , LRG_724:g.41990T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2574T>G MANE Select	ENSP00000269571.4:p.His858Gln
ENST00000269571.9:c.2574T>G	ENSP00000269571.4:p.His858Gln
ENST00000406381.6:c.2484T>G	ENSP00000385185.2:p.His828Gln
ENST00000445658.6:c.1746T>G	ENSP00000404047.2:p.His582Gln
ENST00000541774.5:c.2529T>G	ENSP00000446466.1:p.His843Gln
ENST00000578373.5:c.*2364T>G	ENSP00000463427.1:n.*2364T>G
ENST00000580074.1:c.680T>G
ENST00000583038.5:n.3708T>G
ENST00000584450.5:c.2574T>G	ENSP00000463714.1:p.His858Gln
ENST00000584601.5:c.2484T>G	ENSP00000462438.1:p.His828Gln
NM_001005862.2:c.2484T>G , LRG_724t1:c.2484T>G	NP_001005862.1:p.His828Gln
NM_001289936.1:c.2529T>G , LRG_724t4:c.2529T>G	NP_001276865.1:p.His843Gln
NM_001289937.1:c.2574T>G	NP_001276866.1:p.His858Gln
NM_004448.3:c.2574T>G , LRG_724t2:c.2574T>G	NP_004439.2:p.His858Gln
NR_110535.1:n.2898T>G
XM_024450641.1:c.2712T>G	XP_024306409.1:p.His904Gln
XM_024450642.1:c.2667T>G	XP_024306410.1:p.His889Gln
XM_024450643.1:c.2622T>G	XP_024306411.1:p.His874Gln
NM_001005862.3:c.2484T>G	NP_001005862.1:p.His828Gln
NM_001289936.2:c.2529T>G	NP_001276865.1:p.His843Gln
NM_001289937.2:c.2574T>G	NP_001276866.1:p.His858Gln
NM_001382782.1:c.2484T>G	NP_001369711.1:p.His828Gln
NM_001382783.1:c.2484T>G	NP_001369712.1:p.His828Gln
NM_001382784.1:c.2691T>G	NP_001369713.1:p.His897Gln
NM_001382785.1:c.2676T>G	NP_001369714.1:p.His892Gln
NM_001382786.1:c.2655T>G	NP_001369715.1:p.His885Gln
NM_001382787.1:c.2649T>G	NP_001369716.1:p.His883Gln
NM_001382788.1:c.2604T>G	NP_001369717.1:p.His868Gln
NM_001382789.1:c.2595T>G	NP_001369718.1:p.His865Gln
NM_001382790.1:c.2571T>G	NP_001369719.1:p.His857Gln
NM_001382791.1:c.2565T>G	NP_001369720.1:p.His855Gln
NM_001382792.1:c.2538T>G	NP_001369721.1:p.His846Gln
NM_001382793.1:c.2532T>G	NP_001369722.1:p.His844Gln
NM_001382794.1:c.2532T>G	NP_001369723.1:p.His844Gln
NM_001382795.1:c.2526T>G	NP_001369724.1:p.His842Gln
NM_001382796.1:c.2574T>G	NP_001369725.1:p.His858Gln
NM_001382797.1:c.2475T>G	NP_001369726.1:p.His825Gln
NM_001382798.1:c.2494-198T>G	NP_001369727.1:n.2494-198T>G
NM_001382799.1:c.2394T>G	NP_001369728.1:p.His798Gln
NM_001382800.1:c.2388T>G	NP_001369729.1:p.His796Gln
NM_001382801.1:c.2446-198T>G	NP_001369730.1:n.2446-198T>G
NM_001382802.1:c.2316T>G	NP_001369731.1:p.His772Gln
NM_001382803.1:c.2532T>G	NP_001369732.1:p.His844Gln
NM_001382804.1:c.1746T>G	NP_001369733.1:p.His582Gln
NM_001382805.1:c.2208+1469T>G	NP_001369734.1:n.2208+1469T>G
NM_001382806.1:c.1536T>G	NP_001369735.1:p.His512Gln
NM_004448.4:c.2574T>G MANE Select	NP_004439.2:p.His858Gln
NR_110535.2:n.2812T>G