Canonical Allele Identifier: CA499670898

Gene: ERBB2

Linked Data

• dbSNP Id: rs754308267
• MyVariant Identifiers: chr17:g.37881071T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724818T>A , CM000679.2:g.39724818T>A	GRCh38
NC_000017.10:g.37881071T>A , CM000679.1:g.37881071T>A	GRCh37
NC_000017.9:g.35134597T>A	NCBI36
NG_007503.1:g.41679T>A , LRG_724:g.41679T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2400T>A MANE Select	ENSP00000269571.4:p.Leu800=
ENST00000269571.9:c.2400T>A	ENSP00000269571.4:p.Leu800=
ENST00000406381.6:c.2310T>A	ENSP00000385185.2:p.Leu770=
ENST00000445658.6:c.1572T>A	ENSP00000404047.2:p.Leu524=
ENST00000541774.5:c.2355T>A	ENSP00000446466.1:p.Leu785=
ENST00000578373.5:c.*2190T>A	ENSP00000463427.1:n.*2190T>A
ENST00000580074.1:c.506T>A
ENST00000583038.5:n.3534T>A
ENST00000584450.5:c.2400T>A	ENSP00000463714.1:p.Leu800=
ENST00000584601.5:c.2310T>A	ENSP00000462438.1:p.Leu770=
NM_001005862.2:c.2310T>A , LRG_724t1:c.2310T>A	NP_001005862.1:p.Leu770=
NM_001289936.1:c.2355T>A , LRG_724t4:c.2355T>A	NP_001276865.1:p.Leu785=
NM_001289937.1:c.2400T>A	NP_001276866.1:p.Leu800=
NM_004448.3:c.2400T>A , LRG_724t2:c.2400T>A	NP_004439.2:p.Leu800=
NR_110535.1:n.2724T>A
XM_024450641.1:c.2538T>A	XP_024306409.1:p.Leu846=
XM_024450642.1:c.2493T>A	XP_024306410.1:p.Leu831=
XM_024450643.1:c.2448T>A	XP_024306411.1:p.Leu816=
NM_001005862.3:c.2310T>A	NP_001005862.1:p.Leu770=
NM_001289936.2:c.2355T>A	NP_001276865.1:p.Leu785=
NM_001289937.2:c.2400T>A	NP_001276866.1:p.Leu800=
NM_001382782.1:c.2310T>A	NP_001369711.1:p.Leu770=
NM_001382783.1:c.2310T>A	NP_001369712.1:p.Leu770=
NM_001382784.1:c.2517T>A	NP_001369713.1:p.Leu839=
NM_001382785.1:c.2502T>A	NP_001369714.1:p.Leu834=
NM_001382786.1:c.2481T>A	NP_001369715.1:p.Leu827=
NM_001382787.1:c.2475T>A	NP_001369716.1:p.Leu825=
NM_001382788.1:c.2430T>A	NP_001369717.1:p.Leu810=
NM_001382789.1:c.2421T>A	NP_001369718.1:p.Leu807=
NM_001382790.1:c.2397T>A	NP_001369719.1:p.Leu799=
NM_001382791.1:c.2391T>A	NP_001369720.1:p.Leu797=
NM_001382792.1:c.2364T>A	NP_001369721.1:p.Leu788=
NM_001382793.1:c.2358T>A	NP_001369722.1:p.Leu786=
NM_001382794.1:c.2358T>A	NP_001369723.1:p.Leu786=
NM_001382795.1:c.2352T>A	NP_001369724.1:p.Leu784=
NM_001382796.1:c.2400T>A	NP_001369725.1:p.Leu800=
NM_001382797.1:c.2301T>A	NP_001369726.1:p.Leu767=
NM_001382798.1:c.2400T>A	NP_001369727.1:p.Leu800=
NM_001382799.1:c.2220T>A	NP_001369728.1:p.Leu740=
NM_001382800.1:c.2308-231T>A	NP_001369729.1:n.2308-231T>A
NM_001382801.1:c.2352T>A	NP_001369730.1:p.Leu784=
NM_001382802.1:c.2142T>A	NP_001369731.1:p.Leu714=
NM_001382803.1:c.2358T>A	NP_001369732.1:p.Leu786=
NM_001382804.1:c.1572T>A	NP_001369733.1:p.Leu524=
NM_001382805.1:c.2208+1158T>A	NP_001369734.1:n.2208+1158T>A
NM_001382806.1:c.1362T>A	NP_001369735.1:p.Leu454=
NM_004448.4:c.2400T>A MANE Select	NP_004439.2:p.Leu800=
NR_110535.2:n.2638T>A