Canonical Allele Identifier: CA399302845

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145847414
• MyVariant Identifiers: chr17:g.37880995C>T (hg19) ; chr17:g.39724742C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724742C>T , CM000679.2:g.39724742C>T	GRCh38
NC_000017.10:g.37880995C>T , CM000679.1:g.37880995C>T	GRCh37
NC_000017.9:g.35134521C>T	NCBI36
NG_007503.1:g.41603C>T , LRG_724:g.41603C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2324C>T MANE Select	ENSP00000269571.4:p.Ala775Val
ENST00000269571.9:c.2324C>T	ENSP00000269571.4:p.Ala775Val
ENST00000406381.6:c.2234C>T	ENSP00000385185.2:p.Ala745Val
ENST00000445658.6:c.1496C>T	ENSP00000404047.2:p.Ala499Val
ENST00000541774.5:c.2279C>T	ENSP00000446466.1:p.Ala760Val
ENST00000578373.5:c.*2114C>T	ENSP00000463427.1:n.*2114C>T
ENST00000580074.1:c.430C>T
ENST00000583038.5:n.3458C>T
ENST00000584450.5:c.2324C>T	ENSP00000463714.1:p.Ala775Val
ENST00000584601.5:c.2234C>T	ENSP00000462438.1:p.Ala745Val
NM_001005862.2:c.2234C>T , LRG_724t1:c.2234C>T	NP_001005862.1:p.Ala745Val
NM_001289936.1:c.2279C>T , LRG_724t4:c.2279C>T	NP_001276865.1:p.Ala760Val
NM_001289937.1:c.2324C>T	NP_001276866.1:p.Ala775Val
NM_004448.3:c.2324C>T , LRG_724t2:c.2324C>T	NP_004439.2:p.Ala775Val
NR_110535.1:n.2648C>T
XM_024450641.1:c.2462C>T	XP_024306409.1:p.Ala821Val
XM_024450642.1:c.2417C>T	XP_024306410.1:p.Ala806Val
XM_024450643.1:c.2372C>T	XP_024306411.1:p.Ala791Val
NM_001005862.3:c.2234C>T	NP_001005862.1:p.Ala745Val
NM_001289936.2:c.2279C>T	NP_001276865.1:p.Ala760Val
NM_001289937.2:c.2324C>T	NP_001276866.1:p.Ala775Val
NM_001382782.1:c.2234C>T	NP_001369711.1:p.Ala745Val
NM_001382783.1:c.2234C>T	NP_001369712.1:p.Ala745Val
NM_001382784.1:c.2441C>T	NP_001369713.1:p.Ala814Val
NM_001382785.1:c.2426C>T	NP_001369714.1:p.Ala809Val
NM_001382786.1:c.2405C>T	NP_001369715.1:p.Ala802Val
NM_001382787.1:c.2399C>T	NP_001369716.1:p.Ala800Val
NM_001382788.1:c.2354C>T	NP_001369717.1:p.Ala785Val
NM_001382789.1:c.2345C>T	NP_001369718.1:p.Ala782Val
NM_001382790.1:c.2321C>T	NP_001369719.1:p.Ala774Val
NM_001382791.1:c.2315C>T	NP_001369720.1:p.Ala772Val
NM_001382792.1:c.2288C>T	NP_001369721.1:p.Ala763Val
NM_001382793.1:c.2282C>T	NP_001369722.1:p.Ala761Val
NM_001382794.1:c.2282C>T	NP_001369723.1:p.Ala761Val
NM_001382795.1:c.2276C>T	NP_001369724.1:p.Ala759Val
NM_001382796.1:c.2324C>T	NP_001369725.1:p.Ala775Val
NM_001382797.1:c.2225C>T	NP_001369726.1:p.Ala742Val
NM_001382798.1:c.2324C>T	NP_001369727.1:p.Ala775Val
NM_001382799.1:c.2144C>T	NP_001369728.1:p.Ala715Val
NM_001382800.1:c.2308-307C>T	NP_001369729.1:n.2308-307C>T
NM_001382801.1:c.2276C>T	NP_001369730.1:p.Ala759Val
NM_001382802.1:c.2066C>T	NP_001369731.1:p.Ala689Val
NM_001382803.1:c.2282C>T	NP_001369732.1:p.Ala761Val
NM_001382804.1:c.1496C>T	NP_001369733.1:p.Ala499Val
NM_001382805.1:c.2208+1082C>T	NP_001369734.1:n.2208+1082C>T
NM_001382806.1:c.1286C>T	NP_001369735.1:p.Ala429Val
NM_004448.4:c.2324C>T MANE Select	NP_004439.2:p.Ala775Val
NR_110535.2:n.2562C>T