Canonical Allele Identifier: CA499670833

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145847460
• MyVariant Identifiers: chr17:g.37880996T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724743T>C , CM000679.2:g.39724743T>C	GRCh38
NC_000017.10:g.37880996T>C , CM000679.1:g.37880996T>C	GRCh37
NC_000017.9:g.35134522T>C	NCBI36
NG_007503.1:g.41604T>C , LRG_724:g.41604T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2325T>C MANE Select	ENSP00000269571.4:p.Ala775=
ENST00000269571.9:c.2325T>C	ENSP00000269571.4:p.Ala775=
ENST00000406381.6:c.2235T>C	ENSP00000385185.2:p.Ala745=
ENST00000445658.6:c.1497T>C	ENSP00000404047.2:p.Ala499=
ENST00000541774.5:c.2280T>C	ENSP00000446466.1:p.Ala760=
ENST00000578373.5:c.*2115T>C	ENSP00000463427.1:n.*2115T>C
ENST00000580074.1:c.431T>C
ENST00000583038.5:n.3459T>C
ENST00000584450.5:c.2325T>C	ENSP00000463714.1:p.Ala775=
ENST00000584601.5:c.2235T>C	ENSP00000462438.1:p.Ala745=
NM_001005862.2:c.2235T>C , LRG_724t1:c.2235T>C	NP_001005862.1:p.Ala745=
NM_001289936.1:c.2280T>C , LRG_724t4:c.2280T>C	NP_001276865.1:p.Ala760=
NM_001289937.1:c.2325T>C	NP_001276866.1:p.Ala775=
NM_004448.3:c.2325T>C , LRG_724t2:c.2325T>C	NP_004439.2:p.Ala775=
NR_110535.1:n.2649T>C
XM_024450641.1:c.2463T>C	XP_024306409.1:p.Ala821=
XM_024450642.1:c.2418T>C	XP_024306410.1:p.Ala806=
XM_024450643.1:c.2373T>C	XP_024306411.1:p.Ala791=
NM_001005862.3:c.2235T>C	NP_001005862.1:p.Ala745=
NM_001289936.2:c.2280T>C	NP_001276865.1:p.Ala760=
NM_001289937.2:c.2325T>C	NP_001276866.1:p.Ala775=
NM_001382782.1:c.2235T>C	NP_001369711.1:p.Ala745=
NM_001382783.1:c.2235T>C	NP_001369712.1:p.Ala745=
NM_001382784.1:c.2442T>C	NP_001369713.1:p.Ala814=
NM_001382785.1:c.2427T>C	NP_001369714.1:p.Ala809=
NM_001382786.1:c.2406T>C	NP_001369715.1:p.Ala802=
NM_001382787.1:c.2400T>C	NP_001369716.1:p.Ala800=
NM_001382788.1:c.2355T>C	NP_001369717.1:p.Ala785=
NM_001382789.1:c.2346T>C	NP_001369718.1:p.Ala782=
NM_001382790.1:c.2322T>C	NP_001369719.1:p.Ala774=
NM_001382791.1:c.2316T>C	NP_001369720.1:p.Ala772=
NM_001382792.1:c.2289T>C	NP_001369721.1:p.Ala763=
NM_001382793.1:c.2283T>C	NP_001369722.1:p.Ala761=
NM_001382794.1:c.2283T>C	NP_001369723.1:p.Ala761=
NM_001382795.1:c.2277T>C	NP_001369724.1:p.Ala759=
NM_001382796.1:c.2325T>C	NP_001369725.1:p.Ala775=
NM_001382797.1:c.2226T>C	NP_001369726.1:p.Ala742=
NM_001382798.1:c.2325T>C	NP_001369727.1:p.Ala775=
NM_001382799.1:c.2145T>C	NP_001369728.1:p.Ala715=
NM_001382800.1:c.2308-306T>C	NP_001369729.1:n.2308-306T>C
NM_001382801.1:c.2277T>C	NP_001369730.1:p.Ala759=
NM_001382802.1:c.2067T>C	NP_001369731.1:p.Ala689=
NM_001382803.1:c.2283T>C	NP_001369732.1:p.Ala761=
NM_001382804.1:c.1497T>C	NP_001369733.1:p.Ala499=
NM_001382805.1:c.2208+1083T>C	NP_001369734.1:n.2208+1083T>C
NM_001382806.1:c.1287T>C	NP_001369735.1:p.Ala429=
NM_004448.4:c.2325T>C MANE Select	NP_004439.2:p.Ala775=
NR_110535.2:n.2563T>C