Canonical Allele Identifier: CA399304251

Gene: ERBB2

Linked Data

• dbSNP Id: rs747967722
• MyVariant Identifiers: chr17:g.37881327G>C (hg19) ; chr17:g.39725074G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725074G>C , CM000679.2:g.39725074G>C	GRCh38
NC_000017.10:g.37881327G>C , CM000679.1:g.37881327G>C	GRCh37
NC_000017.9:g.35134853G>C	NCBI36
NG_007503.1:g.41935G>C , LRG_724:g.41935G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2519G>C MANE Select	ENSP00000269571.4:p.Arg840Pro
ENST00000269571.9:c.2519G>C	ENSP00000269571.4:p.Arg840Pro
ENST00000406381.6:c.2429G>C	ENSP00000385185.2:p.Arg810Pro
ENST00000445658.6:c.1691G>C	ENSP00000404047.2:p.Arg564Pro
ENST00000541774.5:c.2474G>C	ENSP00000446466.1:p.Arg825Pro
ENST00000578373.5:c.*2309G>C	ENSP00000463427.1:n.*2309G>C
ENST00000580074.1:c.625G>C
ENST00000583038.5:n.3653G>C
ENST00000584450.5:c.2519G>C	ENSP00000463714.1:p.Arg840Pro
ENST00000584601.5:c.2429G>C	ENSP00000462438.1:p.Arg810Pro
NM_001005862.2:c.2429G>C , LRG_724t1:c.2429G>C	NP_001005862.1:p.Arg810Pro
NM_001289936.1:c.2474G>C , LRG_724t4:c.2474G>C	NP_001276865.1:p.Arg825Pro
NM_001289937.1:c.2519G>C	NP_001276866.1:p.Arg840Pro
NM_004448.3:c.2519G>C , LRG_724t2:c.2519G>C	NP_004439.2:p.Arg840Pro
NR_110535.1:n.2843G>C
XM_024450641.1:c.2657G>C	XP_024306409.1:p.Arg886Pro
XM_024450642.1:c.2612G>C	XP_024306410.1:p.Arg871Pro
XM_024450643.1:c.2567G>C	XP_024306411.1:p.Arg856Pro
NM_001005862.3:c.2429G>C	NP_001005862.1:p.Arg810Pro
NM_001289936.2:c.2474G>C	NP_001276865.1:p.Arg825Pro
NM_001289937.2:c.2519G>C	NP_001276866.1:p.Arg840Pro
NM_001382782.1:c.2429G>C	NP_001369711.1:p.Arg810Pro
NM_001382783.1:c.2429G>C	NP_001369712.1:p.Arg810Pro
NM_001382784.1:c.2636G>C	NP_001369713.1:p.Arg879Pro
NM_001382785.1:c.2621G>C	NP_001369714.1:p.Arg874Pro
NM_001382786.1:c.2600G>C	NP_001369715.1:p.Arg867Pro
NM_001382787.1:c.2594G>C	NP_001369716.1:p.Arg865Pro
NM_001382788.1:c.2549G>C	NP_001369717.1:p.Arg850Pro
NM_001382789.1:c.2540G>C	NP_001369718.1:p.Arg847Pro
NM_001382790.1:c.2516G>C	NP_001369719.1:p.Arg839Pro
NM_001382791.1:c.2510G>C	NP_001369720.1:p.Arg837Pro
NM_001382792.1:c.2483G>C	NP_001369721.1:p.Arg828Pro
NM_001382793.1:c.2477G>C	NP_001369722.1:p.Arg826Pro
NM_001382794.1:c.2477G>C	NP_001369723.1:p.Arg826Pro
NM_001382795.1:c.2471G>C	NP_001369724.1:p.Arg824Pro
NM_001382796.1:c.2519G>C	NP_001369725.1:p.Arg840Pro
NM_001382797.1:c.2420G>C	NP_001369726.1:p.Arg807Pro
NM_001382798.1:c.2493+163G>C	NP_001369727.1:n.2493+163G>C
NM_001382799.1:c.2339G>C	NP_001369728.1:p.Arg780Pro
NM_001382800.1:c.2333G>C	NP_001369729.1:p.Arg778Pro
NM_001382801.1:c.2445+163G>C	NP_001369730.1:n.2445+163G>C
NM_001382802.1:c.2261G>C	NP_001369731.1:p.Arg754Pro
NM_001382803.1:c.2477G>C	NP_001369732.1:p.Arg826Pro
NM_001382804.1:c.1691G>C	NP_001369733.1:p.Arg564Pro
NM_001382805.1:c.2208+1414G>C	NP_001369734.1:n.2208+1414G>C
NM_001382806.1:c.1481G>C	NP_001369735.1:p.Arg494Pro
NM_004448.4:c.2519G>C MANE Select	NP_004439.2:p.Arg840Pro
NR_110535.2:n.2757G>C