Canonical Allele Identifier: CA399303330

Gene: ERBB2

Linked Data

• dbSNP Id: rs755402782
• MyVariant Identifiers: chr17:g.37881079A>C (hg19) ; chr17:g.39724826A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724826A>C , CM000679.2:g.39724826A>C	GRCh38
NC_000017.10:g.37881079A>C , CM000679.1:g.37881079A>C	GRCh37
NC_000017.9:g.35134605A>C	NCBI36
NG_007503.1:g.41687A>C , LRG_724:g.41687A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2408A>C MANE Select	ENSP00000269571.4:p.Tyr803Ser
ENST00000269571.9:c.2408A>C	ENSP00000269571.4:p.Tyr803Ser
ENST00000406381.6:c.2318A>C	ENSP00000385185.2:p.Tyr773Ser
ENST00000445658.6:c.1580A>C	ENSP00000404047.2:p.Tyr527Ser
ENST00000541774.5:c.2363A>C	ENSP00000446466.1:p.Tyr788Ser
ENST00000578373.5:c.*2198A>C	ENSP00000463427.1:n.*2198A>C
ENST00000580074.1:c.514A>C
ENST00000583038.5:n.3542A>C
ENST00000584450.5:c.2408A>C	ENSP00000463714.1:p.Tyr803Ser
ENST00000584601.5:c.2318A>C	ENSP00000462438.1:p.Tyr773Ser
NM_001005862.2:c.2318A>C , LRG_724t1:c.2318A>C	NP_001005862.1:p.Tyr773Ser
NM_001289936.1:c.2363A>C , LRG_724t4:c.2363A>C	NP_001276865.1:p.Tyr788Ser
NM_001289937.1:c.2408A>C	NP_001276866.1:p.Tyr803Ser
NM_004448.3:c.2408A>C , LRG_724t2:c.2408A>C	NP_004439.2:p.Tyr803Ser
NR_110535.1:n.2732A>C
XM_024450641.1:c.2546A>C	XP_024306409.1:p.Tyr849Ser
XM_024450642.1:c.2501A>C	XP_024306410.1:p.Tyr834Ser
XM_024450643.1:c.2456A>C	XP_024306411.1:p.Tyr819Ser
NM_001005862.3:c.2318A>C	NP_001005862.1:p.Tyr773Ser
NM_001289936.2:c.2363A>C	NP_001276865.1:p.Tyr788Ser
NM_001289937.2:c.2408A>C	NP_001276866.1:p.Tyr803Ser
NM_001382782.1:c.2318A>C	NP_001369711.1:p.Tyr773Ser
NM_001382783.1:c.2318A>C	NP_001369712.1:p.Tyr773Ser
NM_001382784.1:c.2525A>C	NP_001369713.1:p.Tyr842Ser
NM_001382785.1:c.2510A>C	NP_001369714.1:p.Tyr837Ser
NM_001382786.1:c.2489A>C	NP_001369715.1:p.Tyr830Ser
NM_001382787.1:c.2483A>C	NP_001369716.1:p.Tyr828Ser
NM_001382788.1:c.2438A>C	NP_001369717.1:p.Tyr813Ser
NM_001382789.1:c.2429A>C	NP_001369718.1:p.Tyr810Ser
NM_001382790.1:c.2405A>C	NP_001369719.1:p.Tyr802Ser
NM_001382791.1:c.2399A>C	NP_001369720.1:p.Tyr800Ser
NM_001382792.1:c.2372A>C	NP_001369721.1:p.Tyr791Ser
NM_001382793.1:c.2366A>C	NP_001369722.1:p.Tyr789Ser
NM_001382794.1:c.2366A>C	NP_001369723.1:p.Tyr789Ser
NM_001382795.1:c.2360A>C	NP_001369724.1:p.Tyr787Ser
NM_001382796.1:c.2408A>C	NP_001369725.1:p.Tyr803Ser
NM_001382797.1:c.2309A>C	NP_001369726.1:p.Tyr770Ser
NM_001382798.1:c.2408A>C	NP_001369727.1:p.Tyr803Ser
NM_001382799.1:c.2228A>C	NP_001369728.1:p.Tyr743Ser
NM_001382800.1:c.2308-223A>C	NP_001369729.1:n.2308-223A>C
NM_001382801.1:c.2360A>C	NP_001369730.1:p.Tyr787Ser
NM_001382802.1:c.2150A>C	NP_001369731.1:p.Tyr717Ser
NM_001382803.1:c.2366A>C	NP_001369732.1:p.Tyr789Ser
NM_001382804.1:c.1580A>C	NP_001369733.1:p.Tyr527Ser
NM_001382805.1:c.2208+1166A>C	NP_001369734.1:n.2208+1166A>C
NM_001382806.1:c.1370A>C	NP_001369735.1:p.Tyr457Ser
NM_004448.4:c.2408A>C MANE Select	NP_004439.2:p.Tyr803Ser
NR_110535.2:n.2646A>C