Canonical Allele Identifier: CA399302925

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2347T>G MANE Select	ENSP00000269571.4:p.Ser783Ala
ENST00000269571.9:c.2347T>G	ENSP00000269571.4:p.Ser783Ala
ENST00000406381.6:c.2257T>G	ENSP00000385185.2:p.Ser753Ala
ENST00000445658.6:c.1519T>G	ENSP00000404047.2:p.Ser507Ala
ENST00000541774.5:c.2302T>G	ENSP00000446466.1:p.Ser768Ala
ENST00000578373.5:c.*2137T>G	ENSP00000463427.1:n.*2137T>G
ENST00000580074.1:c.453T>G
ENST00000583038.5:n.3481T>G
ENST00000584450.5:c.2347T>G	ENSP00000463714.1:p.Ser783Ala
ENST00000584601.5:c.2257T>G	ENSP00000462438.1:p.Ser753Ala
NM_001005862.2:c.2257T>G , LRG_724t1:c.2257T>G	NP_001005862.1:p.Ser753Ala
NM_001289936.1:c.2302T>G , LRG_724t4:c.2302T>G	NP_001276865.1:p.Ser768Ala
NM_001289937.1:c.2347T>G	NP_001276866.1:p.Ser783Ala
NM_004448.3:c.2347T>G , LRG_724t2:c.2347T>G	NP_004439.2:p.Ser783Ala
NR_110535.1:n.2671T>G
XM_024450641.1:c.2485T>G	XP_024306409.1:p.Ser829Ala
XM_024450642.1:c.2440T>G	XP_024306410.1:p.Ser814Ala
XM_024450643.1:c.2395T>G	XP_024306411.1:p.Ser799Ala
NM_001005862.3:c.2257T>G	NP_001005862.1:p.Ser753Ala
NM_001289936.2:c.2302T>G	NP_001276865.1:p.Ser768Ala
NM_001289937.2:c.2347T>G	NP_001276866.1:p.Ser783Ala
NM_001382782.1:c.2257T>G	NP_001369711.1:p.Ser753Ala
NM_001382783.1:c.2257T>G	NP_001369712.1:p.Ser753Ala
NM_001382784.1:c.2464T>G	NP_001369713.1:p.Ser822Ala
NM_001382785.1:c.2449T>G	NP_001369714.1:p.Ser817Ala
NM_001382786.1:c.2428T>G	NP_001369715.1:p.Ser810Ala
NM_001382787.1:c.2422T>G	NP_001369716.1:p.Ser808Ala
NM_001382788.1:c.2377T>G	NP_001369717.1:p.Ser793Ala
NM_001382789.1:c.2368T>G	NP_001369718.1:p.Ser790Ala
NM_001382790.1:c.2344T>G	NP_001369719.1:p.Ser782Ala
NM_001382791.1:c.2338T>G	NP_001369720.1:p.Ser780Ala
NM_001382792.1:c.2311T>G	NP_001369721.1:p.Ser771Ala
NM_001382793.1:c.2305T>G	NP_001369722.1:p.Ser769Ala
NM_001382794.1:c.2305T>G	NP_001369723.1:p.Ser769Ala
NM_001382795.1:c.2299T>G	NP_001369724.1:p.Ser767Ala
NM_001382796.1:c.2347T>G	NP_001369725.1:p.Ser783Ala
NM_001382797.1:c.2248T>G	NP_001369726.1:p.Ser750Ala
NM_001382798.1:c.2347T>G	NP_001369727.1:p.Ser783Ala
NM_001382799.1:c.2167T>G	NP_001369728.1:p.Ser723Ala
NM_001382800.1:c.2308-284T>G	NP_001369729.1:n.2308-284T>G
NM_001382801.1:c.2299T>G	NP_001369730.1:p.Ser767Ala
NM_001382802.1:c.2089T>G	NP_001369731.1:p.Ser697Ala
NM_001382803.1:c.2305T>G	NP_001369732.1:p.Ser769Ala
NM_001382804.1:c.1519T>G	NP_001369733.1:p.Ser507Ala
NM_001382805.1:c.2208+1105T>G	NP_001369734.1:n.2208+1105T>G
NM_001382806.1:c.1309T>G	NP_001369735.1:p.Ser437Ala
NM_004448.4:c.2347T>G MANE Select	NP_004439.2:p.Ser783Ala
NR_110535.2:n.2585T>G