Canonical Allele Identifier: CA399302920

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881018T>A (hg19) ; chr17:g.39724765T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724765T>A , CM000679.2:g.39724765T>A	GRCh38
NC_000017.10:g.37881018T>A , CM000679.1:g.37881018T>A	GRCh37
NC_000017.9:g.35134544T>A	NCBI36
NG_007503.1:g.41626T>A , LRG_724:g.41626T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2347T>A MANE Select	ENSP00000269571.4:p.Ser783Thr
ENST00000269571.9:c.2347T>A	ENSP00000269571.4:p.Ser783Thr
ENST00000406381.6:c.2257T>A	ENSP00000385185.2:p.Ser753Thr
ENST00000445658.6:c.1519T>A	ENSP00000404047.2:p.Ser507Thr
ENST00000541774.5:c.2302T>A	ENSP00000446466.1:p.Ser768Thr
ENST00000578373.5:c.*2137T>A	ENSP00000463427.1:n.*2137T>A
ENST00000580074.1:c.453T>A
ENST00000583038.5:n.3481T>A
ENST00000584450.5:c.2347T>A	ENSP00000463714.1:p.Ser783Thr
ENST00000584601.5:c.2257T>A	ENSP00000462438.1:p.Ser753Thr
NM_001005862.2:c.2257T>A , LRG_724t1:c.2257T>A	NP_001005862.1:p.Ser753Thr
NM_001289936.1:c.2302T>A , LRG_724t4:c.2302T>A	NP_001276865.1:p.Ser768Thr
NM_001289937.1:c.2347T>A	NP_001276866.1:p.Ser783Thr
NM_004448.3:c.2347T>A , LRG_724t2:c.2347T>A	NP_004439.2:p.Ser783Thr
NR_110535.1:n.2671T>A
XM_024450641.1:c.2485T>A	XP_024306409.1:p.Ser829Thr
XM_024450642.1:c.2440T>A	XP_024306410.1:p.Ser814Thr
XM_024450643.1:c.2395T>A	XP_024306411.1:p.Ser799Thr
NM_001005862.3:c.2257T>A	NP_001005862.1:p.Ser753Thr
NM_001289936.2:c.2302T>A	NP_001276865.1:p.Ser768Thr
NM_001289937.2:c.2347T>A	NP_001276866.1:p.Ser783Thr
NM_001382782.1:c.2257T>A	NP_001369711.1:p.Ser753Thr
NM_001382783.1:c.2257T>A	NP_001369712.1:p.Ser753Thr
NM_001382784.1:c.2464T>A	NP_001369713.1:p.Ser822Thr
NM_001382785.1:c.2449T>A	NP_001369714.1:p.Ser817Thr
NM_001382786.1:c.2428T>A	NP_001369715.1:p.Ser810Thr
NM_001382787.1:c.2422T>A	NP_001369716.1:p.Ser808Thr
NM_001382788.1:c.2377T>A	NP_001369717.1:p.Ser793Thr
NM_001382789.1:c.2368T>A	NP_001369718.1:p.Ser790Thr
NM_001382790.1:c.2344T>A	NP_001369719.1:p.Ser782Thr
NM_001382791.1:c.2338T>A	NP_001369720.1:p.Ser780Thr
NM_001382792.1:c.2311T>A	NP_001369721.1:p.Ser771Thr
NM_001382793.1:c.2305T>A	NP_001369722.1:p.Ser769Thr
NM_001382794.1:c.2305T>A	NP_001369723.1:p.Ser769Thr
NM_001382795.1:c.2299T>A	NP_001369724.1:p.Ser767Thr
NM_001382796.1:c.2347T>A	NP_001369725.1:p.Ser783Thr
NM_001382797.1:c.2248T>A	NP_001369726.1:p.Ser750Thr
NM_001382798.1:c.2347T>A	NP_001369727.1:p.Ser783Thr
NM_001382799.1:c.2167T>A	NP_001369728.1:p.Ser723Thr
NM_001382800.1:c.2308-284T>A	NP_001369729.1:n.2308-284T>A
NM_001382801.1:c.2299T>A	NP_001369730.1:p.Ser767Thr
NM_001382802.1:c.2089T>A	NP_001369731.1:p.Ser697Thr
NM_001382803.1:c.2305T>A	NP_001369732.1:p.Ser769Thr
NM_001382804.1:c.1519T>A	NP_001369733.1:p.Ser507Thr
NM_001382805.1:c.2208+1105T>A	NP_001369734.1:n.2208+1105T>A
NM_001382806.1:c.1309T>A	NP_001369735.1:p.Ser437Thr
NM_004448.4:c.2347T>A MANE Select	NP_004439.2:p.Ser783Thr
NR_110535.2:n.2585T>A