Canonical Allele Identifier: CA399303305

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881074G>T (hg19) ; chr17:g.39724821G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724821G>T , CM000679.2:g.39724821G>T	GRCh38
NC_000017.10:g.37881074G>T , CM000679.1:g.37881074G>T	GRCh37
NC_000017.9:g.35134600G>T	NCBI36
NG_007503.1:g.41682G>T , LRG_724:g.41682G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2403G>T MANE Select	ENSP00000269571.4:p.Met801Ile
ENST00000269571.9:c.2403G>T	ENSP00000269571.4:p.Met801Ile
ENST00000406381.6:c.2313G>T	ENSP00000385185.2:p.Met771Ile
ENST00000445658.6:c.1575G>T	ENSP00000404047.2:p.Met525Ile
ENST00000541774.5:c.2358G>T	ENSP00000446466.1:p.Met786Ile
ENST00000578373.5:c.*2193G>T	ENSP00000463427.1:n.*2193G>T
ENST00000580074.1:c.509G>T
ENST00000583038.5:n.3537G>T
ENST00000584450.5:c.2403G>T	ENSP00000463714.1:p.Met801Ile
ENST00000584601.5:c.2313G>T	ENSP00000462438.1:p.Met771Ile
NM_001005862.2:c.2313G>T , LRG_724t1:c.2313G>T	NP_001005862.1:p.Met771Ile
NM_001289936.1:c.2358G>T , LRG_724t4:c.2358G>T	NP_001276865.1:p.Met786Ile
NM_001289937.1:c.2403G>T	NP_001276866.1:p.Met801Ile
NM_004448.3:c.2403G>T , LRG_724t2:c.2403G>T	NP_004439.2:p.Met801Ile
NR_110535.1:n.2727G>T
XM_024450641.1:c.2541G>T	XP_024306409.1:p.Met847Ile
XM_024450642.1:c.2496G>T	XP_024306410.1:p.Met832Ile
XM_024450643.1:c.2451G>T	XP_024306411.1:p.Met817Ile
NM_001005862.3:c.2313G>T	NP_001005862.1:p.Met771Ile
NM_001289936.2:c.2358G>T	NP_001276865.1:p.Met786Ile
NM_001289937.2:c.2403G>T	NP_001276866.1:p.Met801Ile
NM_001382782.1:c.2313G>T	NP_001369711.1:p.Met771Ile
NM_001382783.1:c.2313G>T	NP_001369712.1:p.Met771Ile
NM_001382784.1:c.2520G>T	NP_001369713.1:p.Met840Ile
NM_001382785.1:c.2505G>T	NP_001369714.1:p.Met835Ile
NM_001382786.1:c.2484G>T	NP_001369715.1:p.Met828Ile
NM_001382787.1:c.2478G>T	NP_001369716.1:p.Met826Ile
NM_001382788.1:c.2433G>T	NP_001369717.1:p.Met811Ile
NM_001382789.1:c.2424G>T	NP_001369718.1:p.Met808Ile
NM_001382790.1:c.2400G>T	NP_001369719.1:p.Met800Ile
NM_001382791.1:c.2394G>T	NP_001369720.1:p.Met798Ile
NM_001382792.1:c.2367G>T	NP_001369721.1:p.Met789Ile
NM_001382793.1:c.2361G>T	NP_001369722.1:p.Met787Ile
NM_001382794.1:c.2361G>T	NP_001369723.1:p.Met787Ile
NM_001382795.1:c.2355G>T	NP_001369724.1:p.Met785Ile
NM_001382796.1:c.2403G>T	NP_001369725.1:p.Met801Ile
NM_001382797.1:c.2304G>T	NP_001369726.1:p.Met768Ile
NM_001382798.1:c.2403G>T	NP_001369727.1:p.Met801Ile
NM_001382799.1:c.2223G>T	NP_001369728.1:p.Met741Ile
NM_001382800.1:c.2308-228G>T	NP_001369729.1:n.2308-228G>T
NM_001382801.1:c.2355G>T	NP_001369730.1:p.Met785Ile
NM_001382802.1:c.2145G>T	NP_001369731.1:p.Met715Ile
NM_001382803.1:c.2361G>T	NP_001369732.1:p.Met787Ile
NM_001382804.1:c.1575G>T	NP_001369733.1:p.Met525Ile
NM_001382805.1:c.2208+1161G>T	NP_001369734.1:n.2208+1161G>T
NM_001382806.1:c.1365G>T	NP_001369735.1:p.Met455Ile
NM_004448.4:c.2403G>T MANE Select	NP_004439.2:p.Met801Ile
NR_110535.2:n.2641G>T