Canonical Allele Identifier: CA499890164

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059678289
• MyVariant Identifiers: chr17:g.37881385C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725132C>G , CM000679.2:g.39725132C>G	GRCh38
NC_000017.10:g.37881385C>G , CM000679.1:g.37881385C>G	GRCh37
NC_000017.9:g.35134911C>G	NCBI36
NG_007503.1:g.41993C>G , LRG_724:g.41993C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2577C>G MANE Select	ENSP00000269571.4:p.Val859=
ENST00000269571.9:c.2577C>G	ENSP00000269571.4:p.Val859=
ENST00000406381.6:c.2487C>G	ENSP00000385185.2:p.Val829=
ENST00000445658.6:c.1749C>G	ENSP00000404047.2:p.Val583=
ENST00000541774.5:c.2532C>G	ENSP00000446466.1:p.Val844=
ENST00000578373.5:c.*2367C>G	ENSP00000463427.1:n.*2367C>G
ENST00000580074.1:c.683C>G
ENST00000583038.5:n.3711C>G
ENST00000584450.5:c.2577C>G	ENSP00000463714.1:p.Val859=
ENST00000584601.5:c.2487C>G	ENSP00000462438.1:p.Val829=
NM_001005862.2:c.2487C>G , LRG_724t1:c.2487C>G	NP_001005862.1:p.Val829=
NM_001289936.1:c.2532C>G , LRG_724t4:c.2532C>G	NP_001276865.1:p.Val844=
NM_001289937.1:c.2577C>G	NP_001276866.1:p.Val859=
NM_004448.3:c.2577C>G , LRG_724t2:c.2577C>G	NP_004439.2:p.Val859=
NR_110535.1:n.2901C>G
XM_024450641.1:c.2715C>G	XP_024306409.1:p.Val905=
XM_024450642.1:c.2670C>G	XP_024306410.1:p.Val890=
XM_024450643.1:c.2625C>G	XP_024306411.1:p.Val875=
NM_001005862.3:c.2487C>G	NP_001005862.1:p.Val829=
NM_001289936.2:c.2532C>G	NP_001276865.1:p.Val844=
NM_001289937.2:c.2577C>G	NP_001276866.1:p.Val859=
NM_001382782.1:c.2487C>G	NP_001369711.1:p.Val829=
NM_001382783.1:c.2487C>G	NP_001369712.1:p.Val829=
NM_001382784.1:c.2694C>G	NP_001369713.1:p.Val898=
NM_001382785.1:c.2679C>G	NP_001369714.1:p.Val893=
NM_001382786.1:c.2658C>G	NP_001369715.1:p.Val886=
NM_001382787.1:c.2652C>G	NP_001369716.1:p.Val884=
NM_001382788.1:c.2607C>G	NP_001369717.1:p.Val869=
NM_001382789.1:c.2598C>G	NP_001369718.1:p.Val866=
NM_001382790.1:c.2574C>G	NP_001369719.1:p.Val858=
NM_001382791.1:c.2568C>G	NP_001369720.1:p.Val856=
NM_001382792.1:c.2541C>G	NP_001369721.1:p.Val847=
NM_001382793.1:c.2535C>G	NP_001369722.1:p.Val845=
NM_001382794.1:c.2535C>G	NP_001369723.1:p.Val845=
NM_001382795.1:c.2529C>G	NP_001369724.1:p.Val843=
NM_001382796.1:c.2577C>G	NP_001369725.1:p.Val859=
NM_001382797.1:c.2478C>G	NP_001369726.1:p.Val826=
NM_001382798.1:c.2494-195C>G	NP_001369727.1:n.2494-195C>G
NM_001382799.1:c.2397C>G	NP_001369728.1:p.Val799=
NM_001382800.1:c.2391C>G	NP_001369729.1:p.Val797=
NM_001382801.1:c.2446-195C>G	NP_001369730.1:n.2446-195C>G
NM_001382802.1:c.2319C>G	NP_001369731.1:p.Val773=
NM_001382803.1:c.2535C>G	NP_001369732.1:p.Val845=
NM_001382804.1:c.1749C>G	NP_001369733.1:p.Val583=
NM_001382805.1:c.2208+1472C>G	NP_001369734.1:n.2208+1472C>G
NM_001382806.1:c.1539C>G	NP_001369735.1:p.Val513=
NM_004448.4:c.2577C>G MANE Select	NP_004439.2:p.Val859=
NR_110535.2:n.2815C>G