Canonical Allele Identifier: CA399306504

Gene: ERBB2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725721G>T , CM000679.2:g.39725721G>T	GRCh38
NC_000017.10:g.37881974G>T , CM000679.1:g.37881974G>T	GRCh37
NC_000017.9:g.35135500G>T	NCBI36
NG_007503.1:g.42582G>T , LRG_724:g.42582G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2740G>T MANE Select	ENSP00000269571.4:p.Glu914Ter
ENST00000269571.9:c.2740G>T	ENSP00000269571.4:p.Glu914Ter
ENST00000406381.6:c.2650G>T	ENSP00000385185.2:p.Glu884Ter
ENST00000445658.6:c.1912G>T	ENSP00000404047.2:p.Glu638Ter
ENST00000541774.5:c.2695G>T	ENSP00000446466.1:p.Glu899Ter
ENST00000578373.5:c.*2530G>T	ENSP00000463427.1:n.*2530G>T
ENST00000583038.5:n.4300G>T
ENST00000584450.5:c.2740G>T	ENSP00000463714.1:p.Glu914Ter
ENST00000584601.5:c.2650G>T	ENSP00000462438.1:p.Glu884Ter
NM_001005862.2:c.2650G>T , LRG_724t1:c.2650G>T	NP_001005862.1:p.Glu884Ter
NM_001289936.1:c.2695G>T , LRG_724t4:c.2695G>T	NP_001276865.1:p.Glu899Ter
NM_001289937.1:c.2740G>T	NP_001276866.1:p.Glu914Ter
NM_004448.3:c.2740G>T , LRG_724t2:c.2740G>T	NP_004439.2:p.Glu914Ter
NR_110535.1:n.3064G>T
XM_024450641.1:c.2878G>T	XP_024306409.1:p.Glu960Ter
XM_024450642.1:c.2833G>T	XP_024306410.1:p.Glu945Ter
XM_024450643.1:c.2788G>T	XP_024306411.1:p.Glu930Ter
NM_001005862.3:c.2650G>T	NP_001005862.1:p.Glu884Ter
NM_001289936.2:c.2695G>T	NP_001276865.1:p.Glu899Ter
NM_001289937.2:c.2740G>T	NP_001276866.1:p.Glu914Ter
NM_001382782.1:c.2650G>T	NP_001369711.1:p.Glu884Ter
NM_001382783.1:c.2650G>T	NP_001369712.1:p.Glu884Ter
NM_001382784.1:c.2857G>T	NP_001369713.1:p.Glu953Ter
NM_001382785.1:c.2842G>T	NP_001369714.1:p.Glu948Ter
NM_001382786.1:c.2821G>T	NP_001369715.1:p.Glu941Ter
NM_001382787.1:c.2815G>T	NP_001369716.1:p.Glu939Ter
NM_001382788.1:c.2770G>T	NP_001369717.1:p.Glu924Ter
NM_001382789.1:c.2761G>T	NP_001369718.1:p.Glu921Ter
NM_001382790.1:c.2737G>T	NP_001369719.1:p.Glu913Ter
NM_001382791.1:c.2731G>T	NP_001369720.1:p.Glu911Ter
NM_001382792.1:c.2704G>T	NP_001369721.1:p.Glu902Ter
NM_001382793.1:c.2698G>T	NP_001369722.1:p.Glu900Ter
NM_001382794.1:c.2698G>T	NP_001369723.1:p.Glu900Ter
NM_001382795.1:c.2692G>T	NP_001369724.1:p.Glu898Ter
NM_001382796.1:c.2740G>T	NP_001369725.1:p.Glu914Ter
NM_001382797.1:c.2641G>T	NP_001369726.1:p.Glu881Ter
NM_001382798.1:c.2584G>T	NP_001369727.1:p.Glu862Ter
NM_001382799.1:c.2560G>T	NP_001369728.1:p.Glu854Ter
NM_001382800.1:c.2554G>T	NP_001369729.1:p.Glu852Ter
NM_001382801.1:c.2536G>T	NP_001369730.1:p.Glu846Ter
NM_001382802.1:c.2482G>T	NP_001369731.1:p.Glu828Ter
NM_001382803.1:c.2698G>T	NP_001369732.1:p.Glu900Ter
NM_001382804.1:c.1912G>T	NP_001369733.1:p.Glu638Ter
NM_001382805.1:c.2209-1574G>T	NP_001369734.1:n.2209-1574G>T
NM_001382806.1:c.1702G>T	NP_001369735.1:p.Glu568Ter
NM_004448.4:c.2740G>T MANE Select	NP_004439.2:p.Glu914Ter
NR_110535.2:n.2978G>T