Canonical Allele Identifier: CA499670863

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145848946
• MyVariant Identifiers: chr17:g.37881026T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724773T>C , CM000679.2:g.39724773T>C	GRCh38
NC_000017.10:g.37881026T>C , CM000679.1:g.37881026T>C	GRCh37
NC_000017.9:g.35134552T>C	NCBI36
NG_007503.1:g.41634T>C , LRG_724:g.41634T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2355T>C MANE Select	ENSP00000269571.4:p.Leu785=
ENST00000269571.9:c.2355T>C	ENSP00000269571.4:p.Leu785=
ENST00000406381.6:c.2265T>C	ENSP00000385185.2:p.Leu755=
ENST00000445658.6:c.1527T>C	ENSP00000404047.2:p.Leu509=
ENST00000541774.5:c.2310T>C	ENSP00000446466.1:p.Leu770=
ENST00000578373.5:c.*2145T>C	ENSP00000463427.1:n.*2145T>C
ENST00000580074.1:c.461T>C
ENST00000583038.5:n.3489T>C
ENST00000584450.5:c.2355T>C	ENSP00000463714.1:p.Leu785=
ENST00000584601.5:c.2265T>C	ENSP00000462438.1:p.Leu755=
NM_001005862.2:c.2265T>C , LRG_724t1:c.2265T>C	NP_001005862.1:p.Leu755=
NM_001289936.1:c.2310T>C , LRG_724t4:c.2310T>C	NP_001276865.1:p.Leu770=
NM_001289937.1:c.2355T>C	NP_001276866.1:p.Leu785=
NM_004448.3:c.2355T>C , LRG_724t2:c.2355T>C	NP_004439.2:p.Leu785=
NR_110535.1:n.2679T>C
XM_024450641.1:c.2493T>C	XP_024306409.1:p.Leu831=
XM_024450642.1:c.2448T>C	XP_024306410.1:p.Leu816=
XM_024450643.1:c.2403T>C	XP_024306411.1:p.Leu801=
NM_001005862.3:c.2265T>C	NP_001005862.1:p.Leu755=
NM_001289936.2:c.2310T>C	NP_001276865.1:p.Leu770=
NM_001289937.2:c.2355T>C	NP_001276866.1:p.Leu785=
NM_001382782.1:c.2265T>C	NP_001369711.1:p.Leu755=
NM_001382783.1:c.2265T>C	NP_001369712.1:p.Leu755=
NM_001382784.1:c.2472T>C	NP_001369713.1:p.Leu824=
NM_001382785.1:c.2457T>C	NP_001369714.1:p.Leu819=
NM_001382786.1:c.2436T>C	NP_001369715.1:p.Leu812=
NM_001382787.1:c.2430T>C	NP_001369716.1:p.Leu810=
NM_001382788.1:c.2385T>C	NP_001369717.1:p.Leu795=
NM_001382789.1:c.2376T>C	NP_001369718.1:p.Leu792=
NM_001382790.1:c.2352T>C	NP_001369719.1:p.Leu784=
NM_001382791.1:c.2346T>C	NP_001369720.1:p.Leu782=
NM_001382792.1:c.2319T>C	NP_001369721.1:p.Leu773=
NM_001382793.1:c.2313T>C	NP_001369722.1:p.Leu771=
NM_001382794.1:c.2313T>C	NP_001369723.1:p.Leu771=
NM_001382795.1:c.2307T>C	NP_001369724.1:p.Leu769=
NM_001382796.1:c.2355T>C	NP_001369725.1:p.Leu785=
NM_001382797.1:c.2256T>C	NP_001369726.1:p.Leu752=
NM_001382798.1:c.2355T>C	NP_001369727.1:p.Leu785=
NM_001382799.1:c.2175T>C	NP_001369728.1:p.Leu725=
NM_001382800.1:c.2308-276T>C	NP_001369729.1:n.2308-276T>C
NM_001382801.1:c.2307T>C	NP_001369730.1:p.Leu769=
NM_001382802.1:c.2097T>C	NP_001369731.1:p.Leu699=
NM_001382803.1:c.2313T>C	NP_001369732.1:p.Leu771=
NM_001382804.1:c.1527T>C	NP_001369733.1:p.Leu509=
NM_001382805.1:c.2208+1113T>C	NP_001369734.1:n.2208+1113T>C
NM_001382806.1:c.1317T>C	NP_001369735.1:p.Leu439=
NM_004448.4:c.2355T>C MANE Select	NP_004439.2:p.Leu785=
NR_110535.2:n.2593T>C