Canonical Allele Identifier: CA399304597

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881375C>A (hg19) ; chr17:g.39725122C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725122C>A , CM000679.2:g.39725122C>A	GRCh38
NC_000017.10:g.37881375C>A , CM000679.1:g.37881375C>A	GRCh37
NC_000017.9:g.35134901C>A	NCBI36
NG_007503.1:g.41983C>A , LRG_724:g.41983C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2567C>A MANE Select	ENSP00000269571.4:p.Pro856His
ENST00000269571.9:c.2567C>A	ENSP00000269571.4:p.Pro856His
ENST00000406381.6:c.2477C>A	ENSP00000385185.2:p.Pro826His
ENST00000445658.6:c.1739C>A	ENSP00000404047.2:p.Pro580His
ENST00000541774.5:c.2522C>A	ENSP00000446466.1:p.Pro841His
ENST00000578373.5:c.*2357C>A	ENSP00000463427.1:n.*2357C>A
ENST00000580074.1:c.673C>A
ENST00000583038.5:n.3701C>A
ENST00000584450.5:c.2567C>A	ENSP00000463714.1:p.Pro856His
ENST00000584601.5:c.2477C>A	ENSP00000462438.1:p.Pro826His
NM_001005862.2:c.2477C>A , LRG_724t1:c.2477C>A	NP_001005862.1:p.Pro826His
NM_001289936.1:c.2522C>A , LRG_724t4:c.2522C>A	NP_001276865.1:p.Pro841His
NM_001289937.1:c.2567C>A	NP_001276866.1:p.Pro856His
NM_004448.3:c.2567C>A , LRG_724t2:c.2567C>A	NP_004439.2:p.Pro856His
NR_110535.1:n.2891C>A
XM_024450641.1:c.2705C>A	XP_024306409.1:p.Pro902His
XM_024450642.1:c.2660C>A	XP_024306410.1:p.Pro887His
XM_024450643.1:c.2615C>A	XP_024306411.1:p.Pro872His
NM_001005862.3:c.2477C>A	NP_001005862.1:p.Pro826His
NM_001289936.2:c.2522C>A	NP_001276865.1:p.Pro841His
NM_001289937.2:c.2567C>A	NP_001276866.1:p.Pro856His
NM_001382782.1:c.2477C>A	NP_001369711.1:p.Pro826His
NM_001382783.1:c.2477C>A	NP_001369712.1:p.Pro826His
NM_001382784.1:c.2684C>A	NP_001369713.1:p.Pro895His
NM_001382785.1:c.2669C>A	NP_001369714.1:p.Pro890His
NM_001382786.1:c.2648C>A	NP_001369715.1:p.Pro883His
NM_001382787.1:c.2642C>A	NP_001369716.1:p.Pro881His
NM_001382788.1:c.2597C>A	NP_001369717.1:p.Pro866His
NM_001382789.1:c.2588C>A	NP_001369718.1:p.Pro863His
NM_001382790.1:c.2564C>A	NP_001369719.1:p.Pro855His
NM_001382791.1:c.2558C>A	NP_001369720.1:p.Pro853His
NM_001382792.1:c.2531C>A	NP_001369721.1:p.Pro844His
NM_001382793.1:c.2525C>A	NP_001369722.1:p.Pro842His
NM_001382794.1:c.2525C>A	NP_001369723.1:p.Pro842His
NM_001382795.1:c.2519C>A	NP_001369724.1:p.Pro840His
NM_001382796.1:c.2567C>A	NP_001369725.1:p.Pro856His
NM_001382797.1:c.2468C>A	NP_001369726.1:p.Pro823His
NM_001382798.1:c.2494-205C>A	NP_001369727.1:n.2494-205C>A
NM_001382799.1:c.2387C>A	NP_001369728.1:p.Pro796His
NM_001382800.1:c.2381C>A	NP_001369729.1:p.Pro794His
NM_001382801.1:c.2446-205C>A	NP_001369730.1:n.2446-205C>A
NM_001382802.1:c.2309C>A	NP_001369731.1:p.Pro770His
NM_001382803.1:c.2525C>A	NP_001369732.1:p.Pro842His
NM_001382804.1:c.1739C>A	NP_001369733.1:p.Pro580His
NM_001382805.1:c.2208+1462C>A	NP_001369734.1:n.2208+1462C>A
NM_001382806.1:c.1529C>A	NP_001369735.1:p.Pro510His
NM_004448.4:c.2567C>A MANE Select	NP_004439.2:p.Pro856His
NR_110535.2:n.2805C>A