Canonical Allele Identifier: CA399303454

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881099G>T (hg19) ; chr17:g.39724846G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724846G>T , CM000679.2:g.39724846G>T	GRCh38
NC_000017.10:g.37881099G>T , CM000679.1:g.37881099G>T	GRCh37
NC_000017.9:g.35134625G>T	NCBI36
NG_007503.1:g.41707G>T , LRG_724:g.41707G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2428G>T MANE Select	ENSP00000269571.4:p.Val810Phe
ENST00000269571.9:c.2428G>T	ENSP00000269571.4:p.Val810Phe
ENST00000406381.6:c.2338G>T	ENSP00000385185.2:p.Val780Phe
ENST00000445658.6:c.1600G>T	ENSP00000404047.2:p.Val534Phe
ENST00000541774.5:c.2383G>T	ENSP00000446466.1:p.Val795Phe
ENST00000578373.5:c.*2218G>T	ENSP00000463427.1:n.*2218G>T
ENST00000580074.1:c.534G>T
ENST00000583038.5:n.3562G>T
ENST00000584450.5:c.2428G>T	ENSP00000463714.1:p.Val810Phe
ENST00000584601.5:c.2338G>T	ENSP00000462438.1:p.Val780Phe
NM_001005862.2:c.2338G>T , LRG_724t1:c.2338G>T	NP_001005862.1:p.Val780Phe
NM_001289936.1:c.2383G>T , LRG_724t4:c.2383G>T	NP_001276865.1:p.Val795Phe
NM_001289937.1:c.2428G>T	NP_001276866.1:p.Val810Phe
NM_004448.3:c.2428G>T , LRG_724t2:c.2428G>T	NP_004439.2:p.Val810Phe
NR_110535.1:n.2752G>T
XM_024450641.1:c.2566G>T	XP_024306409.1:p.Val856Phe
XM_024450642.1:c.2521G>T	XP_024306410.1:p.Val841Phe
XM_024450643.1:c.2476G>T	XP_024306411.1:p.Val826Phe
NM_001005862.3:c.2338G>T	NP_001005862.1:p.Val780Phe
NM_001289936.2:c.2383G>T	NP_001276865.1:p.Val795Phe
NM_001289937.2:c.2428G>T	NP_001276866.1:p.Val810Phe
NM_001382782.1:c.2338G>T	NP_001369711.1:p.Val780Phe
NM_001382783.1:c.2338G>T	NP_001369712.1:p.Val780Phe
NM_001382784.1:c.2545G>T	NP_001369713.1:p.Val849Phe
NM_001382785.1:c.2530G>T	NP_001369714.1:p.Val844Phe
NM_001382786.1:c.2509G>T	NP_001369715.1:p.Val837Phe
NM_001382787.1:c.2503G>T	NP_001369716.1:p.Val835Phe
NM_001382788.1:c.2458G>T	NP_001369717.1:p.Val820Phe
NM_001382789.1:c.2449G>T	NP_001369718.1:p.Val817Phe
NM_001382790.1:c.2425G>T	NP_001369719.1:p.Val809Phe
NM_001382791.1:c.2419G>T	NP_001369720.1:p.Val807Phe
NM_001382792.1:c.2392G>T	NP_001369721.1:p.Val798Phe
NM_001382793.1:c.2386G>T	NP_001369722.1:p.Val796Phe
NM_001382794.1:c.2386G>T	NP_001369723.1:p.Val796Phe
NM_001382795.1:c.2380G>T	NP_001369724.1:p.Val794Phe
NM_001382796.1:c.2428G>T	NP_001369725.1:p.Val810Phe
NM_001382797.1:c.2329G>T	NP_001369726.1:p.Val777Phe
NM_001382798.1:c.2428G>T	NP_001369727.1:p.Val810Phe
NM_001382799.1:c.2248G>T	NP_001369728.1:p.Val750Phe
NM_001382800.1:c.2308-203G>T	NP_001369729.1:n.2308-203G>T
NM_001382801.1:c.2380G>T	NP_001369730.1:p.Val794Phe
NM_001382802.1:c.2170G>T	NP_001369731.1:p.Val724Phe
NM_001382803.1:c.2386G>T	NP_001369732.1:p.Val796Phe
NM_001382804.1:c.1600G>T	NP_001369733.1:p.Val534Phe
NM_001382805.1:c.2208+1186G>T	NP_001369734.1:n.2208+1186G>T
NM_001382806.1:c.1390G>T	NP_001369735.1:p.Val464Phe
NM_004448.4:c.2428G>T MANE Select	NP_004439.2:p.Val810Phe
NR_110535.2:n.2666G>T