Canonical Allele Identifier: CA399304157

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145862672
• MyVariant Identifiers: chr17:g.37881319G>C (hg19) ; chr17:g.39725066G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725066G>C , CM000679.2:g.39725066G>C	GRCh38
NC_000017.10:g.37881319G>C , CM000679.1:g.37881319G>C	GRCh37
NC_000017.9:g.35134845G>C	NCBI36
NG_007503.1:g.41927G>C , LRG_724:g.41927G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2511G>C MANE Select	ENSP00000269571.4:p.Glu837Asp
ENST00000269571.9:c.2511G>C	ENSP00000269571.4:p.Glu837Asp
ENST00000406381.6:c.2421G>C	ENSP00000385185.2:p.Glu807Asp
ENST00000445658.6:c.1683G>C	ENSP00000404047.2:p.Glu561Asp
ENST00000541774.5:c.2466G>C	ENSP00000446466.1:p.Glu822Asp
ENST00000578373.5:c.*2301G>C	ENSP00000463427.1:n.*2301G>C
ENST00000580074.1:c.617G>C
ENST00000583038.5:n.3645G>C
ENST00000584450.5:c.2511G>C	ENSP00000463714.1:p.Glu837Asp
ENST00000584601.5:c.2421G>C	ENSP00000462438.1:p.Glu807Asp
NM_001005862.2:c.2421G>C , LRG_724t1:c.2421G>C	NP_001005862.1:p.Glu807Asp
NM_001289936.1:c.2466G>C , LRG_724t4:c.2466G>C	NP_001276865.1:p.Glu822Asp
NM_001289937.1:c.2511G>C	NP_001276866.1:p.Glu837Asp
NM_004448.3:c.2511G>C , LRG_724t2:c.2511G>C	NP_004439.2:p.Glu837Asp
NR_110535.1:n.2835G>C
XM_024450641.1:c.2649G>C	XP_024306409.1:p.Glu883Asp
XM_024450642.1:c.2604G>C	XP_024306410.1:p.Glu868Asp
XM_024450643.1:c.2559G>C	XP_024306411.1:p.Glu853Asp
NM_001005862.3:c.2421G>C	NP_001005862.1:p.Glu807Asp
NM_001289936.2:c.2466G>C	NP_001276865.1:p.Glu822Asp
NM_001289937.2:c.2511G>C	NP_001276866.1:p.Glu837Asp
NM_001382782.1:c.2421G>C	NP_001369711.1:p.Glu807Asp
NM_001382783.1:c.2421G>C	NP_001369712.1:p.Glu807Asp
NM_001382784.1:c.2628G>C	NP_001369713.1:p.Glu876Asp
NM_001382785.1:c.2613G>C	NP_001369714.1:p.Glu871Asp
NM_001382786.1:c.2592G>C	NP_001369715.1:p.Glu864Asp
NM_001382787.1:c.2586G>C	NP_001369716.1:p.Glu862Asp
NM_001382788.1:c.2541G>C	NP_001369717.1:p.Glu847Asp
NM_001382789.1:c.2532G>C	NP_001369718.1:p.Glu844Asp
NM_001382790.1:c.2508G>C	NP_001369719.1:p.Glu836Asp
NM_001382791.1:c.2502G>C	NP_001369720.1:p.Glu834Asp
NM_001382792.1:c.2475G>C	NP_001369721.1:p.Glu825Asp
NM_001382793.1:c.2469G>C	NP_001369722.1:p.Glu823Asp
NM_001382794.1:c.2469G>C	NP_001369723.1:p.Glu823Asp
NM_001382795.1:c.2463G>C	NP_001369724.1:p.Glu821Asp
NM_001382796.1:c.2511G>C	NP_001369725.1:p.Glu837Asp
NM_001382797.1:c.2412G>C	NP_001369726.1:p.Glu804Asp
NM_001382798.1:c.2493+155G>C	NP_001369727.1:n.2493+155G>C
NM_001382799.1:c.2331G>C	NP_001369728.1:p.Glu777Asp
NM_001382800.1:c.2325G>C	NP_001369729.1:p.Glu775Asp
NM_001382801.1:c.2445+155G>C	NP_001369730.1:n.2445+155G>C
NM_001382802.1:c.2253G>C	NP_001369731.1:p.Glu751Asp
NM_001382803.1:c.2469G>C	NP_001369732.1:p.Glu823Asp
NM_001382804.1:c.1683G>C	NP_001369733.1:p.Glu561Asp
NM_001382805.1:c.2208+1406G>C	NP_001369734.1:n.2208+1406G>C
NM_001382806.1:c.1473G>C	NP_001369735.1:p.Glu491Asp
NM_004448.4:c.2511G>C MANE Select	NP_004439.2:p.Glu837Asp
NR_110535.2:n.2749G>C