Canonical Allele Identifier: CA399303131

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849776
• MyVariant Identifiers: chr17:g.37881048A>C (hg19) ; chr17:g.39724795A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724795A>C , CM000679.2:g.39724795A>C	GRCh38
NC_000017.10:g.37881048A>C , CM000679.1:g.37881048A>C	GRCh37
NC_000017.9:g.35134574A>C	NCBI36
NG_007503.1:g.41656A>C , LRG_724:g.41656A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2377A>C MANE Select	ENSP00000269571.4:p.Thr793Pro
ENST00000269571.9:c.2377A>C	ENSP00000269571.4:p.Thr793Pro
ENST00000406381.6:c.2287A>C	ENSP00000385185.2:p.Thr763Pro
ENST00000445658.6:c.1549A>C	ENSP00000404047.2:p.Thr517Pro
ENST00000541774.5:c.2332A>C	ENSP00000446466.1:p.Thr778Pro
ENST00000578373.5:c.*2167A>C	ENSP00000463427.1:n.*2167A>C
ENST00000580074.1:c.483A>C
ENST00000583038.5:n.3511A>C
ENST00000584450.5:c.2377A>C	ENSP00000463714.1:p.Thr793Pro
ENST00000584601.5:c.2287A>C	ENSP00000462438.1:p.Thr763Pro
NM_001005862.2:c.2287A>C , LRG_724t1:c.2287A>C	NP_001005862.1:p.Thr763Pro
NM_001289936.1:c.2332A>C , LRG_724t4:c.2332A>C	NP_001276865.1:p.Thr778Pro
NM_001289937.1:c.2377A>C	NP_001276866.1:p.Thr793Pro
NM_004448.3:c.2377A>C , LRG_724t2:c.2377A>C	NP_004439.2:p.Thr793Pro
NR_110535.1:n.2701A>C
XM_024450641.1:c.2515A>C	XP_024306409.1:p.Thr839Pro
XM_024450642.1:c.2470A>C	XP_024306410.1:p.Thr824Pro
XM_024450643.1:c.2425A>C	XP_024306411.1:p.Thr809Pro
NM_001005862.3:c.2287A>C	NP_001005862.1:p.Thr763Pro
NM_001289936.2:c.2332A>C	NP_001276865.1:p.Thr778Pro
NM_001289937.2:c.2377A>C	NP_001276866.1:p.Thr793Pro
NM_001382782.1:c.2287A>C	NP_001369711.1:p.Thr763Pro
NM_001382783.1:c.2287A>C	NP_001369712.1:p.Thr763Pro
NM_001382784.1:c.2494A>C	NP_001369713.1:p.Thr832Pro
NM_001382785.1:c.2479A>C	NP_001369714.1:p.Thr827Pro
NM_001382786.1:c.2458A>C	NP_001369715.1:p.Thr820Pro
NM_001382787.1:c.2452A>C	NP_001369716.1:p.Thr818Pro
NM_001382788.1:c.2407A>C	NP_001369717.1:p.Thr803Pro
NM_001382789.1:c.2398A>C	NP_001369718.1:p.Thr800Pro
NM_001382790.1:c.2374A>C	NP_001369719.1:p.Thr792Pro
NM_001382791.1:c.2368A>C	NP_001369720.1:p.Thr790Pro
NM_001382792.1:c.2341A>C	NP_001369721.1:p.Thr781Pro
NM_001382793.1:c.2335A>C	NP_001369722.1:p.Thr779Pro
NM_001382794.1:c.2335A>C	NP_001369723.1:p.Thr779Pro
NM_001382795.1:c.2329A>C	NP_001369724.1:p.Thr777Pro
NM_001382796.1:c.2377A>C	NP_001369725.1:p.Thr793Pro
NM_001382797.1:c.2278A>C	NP_001369726.1:p.Thr760Pro
NM_001382798.1:c.2377A>C	NP_001369727.1:p.Thr793Pro
NM_001382799.1:c.2197A>C	NP_001369728.1:p.Thr733Pro
NM_001382800.1:c.2308-254A>C	NP_001369729.1:n.2308-254A>C
NM_001382801.1:c.2329A>C	NP_001369730.1:p.Thr777Pro
NM_001382802.1:c.2119A>C	NP_001369731.1:p.Thr707Pro
NM_001382803.1:c.2335A>C	NP_001369732.1:p.Thr779Pro
NM_001382804.1:c.1549A>C	NP_001369733.1:p.Thr517Pro
NM_001382805.1:c.2208+1135A>C	NP_001369734.1:n.2208+1135A>C
NM_001382806.1:c.1339A>C	NP_001369735.1:p.Thr447Pro
NM_004448.4:c.2377A>C MANE Select	NP_004439.2:p.Thr793Pro
NR_110535.2:n.2615A>C