Canonical Allele Identifier: CA399303136

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2377A>T MANE Select	ENSP00000269571.4:p.Thr793Ser
ENST00000269571.9:c.2377A>T	ENSP00000269571.4:p.Thr793Ser
ENST00000406381.6:c.2287A>T	ENSP00000385185.2:p.Thr763Ser
ENST00000445658.6:c.1549A>T	ENSP00000404047.2:p.Thr517Ser
ENST00000541774.5:c.2332A>T	ENSP00000446466.1:p.Thr778Ser
ENST00000578373.5:c.*2167A>T	ENSP00000463427.1:n.*2167A>T
ENST00000580074.1:c.483A>T
ENST00000583038.5:n.3511A>T
ENST00000584450.5:c.2377A>T	ENSP00000463714.1:p.Thr793Ser
ENST00000584601.5:c.2287A>T	ENSP00000462438.1:p.Thr763Ser
NM_001005862.2:c.2287A>T , LRG_724t1:c.2287A>T	NP_001005862.1:p.Thr763Ser
NM_001289936.1:c.2332A>T , LRG_724t4:c.2332A>T	NP_001276865.1:p.Thr778Ser
NM_001289937.1:c.2377A>T	NP_001276866.1:p.Thr793Ser
NM_004448.3:c.2377A>T , LRG_724t2:c.2377A>T	NP_004439.2:p.Thr793Ser
NR_110535.1:n.2701A>T
XM_024450641.1:c.2515A>T	XP_024306409.1:p.Thr839Ser
XM_024450642.1:c.2470A>T	XP_024306410.1:p.Thr824Ser
XM_024450643.1:c.2425A>T	XP_024306411.1:p.Thr809Ser
NM_001005862.3:c.2287A>T	NP_001005862.1:p.Thr763Ser
NM_001289936.2:c.2332A>T	NP_001276865.1:p.Thr778Ser
NM_001289937.2:c.2377A>T	NP_001276866.1:p.Thr793Ser
NM_001382782.1:c.2287A>T	NP_001369711.1:p.Thr763Ser
NM_001382783.1:c.2287A>T	NP_001369712.1:p.Thr763Ser
NM_001382784.1:c.2494A>T	NP_001369713.1:p.Thr832Ser
NM_001382785.1:c.2479A>T	NP_001369714.1:p.Thr827Ser
NM_001382786.1:c.2458A>T	NP_001369715.1:p.Thr820Ser
NM_001382787.1:c.2452A>T	NP_001369716.1:p.Thr818Ser
NM_001382788.1:c.2407A>T	NP_001369717.1:p.Thr803Ser
NM_001382789.1:c.2398A>T	NP_001369718.1:p.Thr800Ser
NM_001382790.1:c.2374A>T	NP_001369719.1:p.Thr792Ser
NM_001382791.1:c.2368A>T	NP_001369720.1:p.Thr790Ser
NM_001382792.1:c.2341A>T	NP_001369721.1:p.Thr781Ser
NM_001382793.1:c.2335A>T	NP_001369722.1:p.Thr779Ser
NM_001382794.1:c.2335A>T	NP_001369723.1:p.Thr779Ser
NM_001382795.1:c.2329A>T	NP_001369724.1:p.Thr777Ser
NM_001382796.1:c.2377A>T	NP_001369725.1:p.Thr793Ser
NM_001382797.1:c.2278A>T	NP_001369726.1:p.Thr760Ser
NM_001382798.1:c.2377A>T	NP_001369727.1:p.Thr793Ser
NM_001382799.1:c.2197A>T	NP_001369728.1:p.Thr733Ser
NM_001382800.1:c.2308-254A>T	NP_001369729.1:n.2308-254A>T
NM_001382801.1:c.2329A>T	NP_001369730.1:p.Thr777Ser
NM_001382802.1:c.2119A>T	NP_001369731.1:p.Thr707Ser
NM_001382803.1:c.2335A>T	NP_001369732.1:p.Thr779Ser
NM_001382804.1:c.1549A>T	NP_001369733.1:p.Thr517Ser
NM_001382805.1:c.2208+1135A>T	NP_001369734.1:n.2208+1135A>T
NM_001382806.1:c.1339A>T	NP_001369735.1:p.Thr447Ser
NM_004448.4:c.2377A>T MANE Select	NP_004439.2:p.Thr793Ser
NR_110535.2:n.2615A>T