Canonical Allele Identifier: CA399302850

Gene: ERBB2

Linked Data

• dbSNP Id: rs28933369
• COSMIC: COSM303938
• MyVariant Identifiers: chr17:g.37880997G>T (hg19) ; chr17:g.39724744G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724744G>T , CM000679.2:g.39724744G>T	GRCh38
NC_000017.10:g.37880997G>T , CM000679.1:g.37880997G>T	GRCh37
NC_000017.9:g.35134523G>T	NCBI36
NG_007503.1:g.41605G>T , LRG_724:g.41605G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2326G>T MANE Select	ENSP00000269571.4:p.Gly776Cys
ENST00000269571.9:c.2326G>T	ENSP00000269571.4:p.Gly776Cys
ENST00000406381.6:c.2236G>T	ENSP00000385185.2:p.Gly746Cys
ENST00000445658.6:c.1498G>T	ENSP00000404047.2:p.Gly500Cys
ENST00000541774.5:c.2281G>T	ENSP00000446466.1:p.Gly761Cys
ENST00000578373.5:c.*2116G>T	ENSP00000463427.1:n.*2116G>T
ENST00000580074.1:c.432G>T
ENST00000583038.5:n.3460G>T
ENST00000584450.5:c.2326G>T	ENSP00000463714.1:p.Gly776Cys
ENST00000584601.5:c.2236G>T	ENSP00000462438.1:p.Gly746Cys
NM_001005862.2:c.2236G>T , LRG_724t1:c.2236G>T	NP_001005862.1:p.Gly746Cys
NM_001289936.1:c.2281G>T , LRG_724t4:c.2281G>T	NP_001276865.1:p.Gly761Cys
NM_001289937.1:c.2326G>T	NP_001276866.1:p.Gly776Cys
NM_004448.3:c.2326G>T , LRG_724t2:c.2326G>T	NP_004439.2:p.Gly776Cys
NR_110535.1:n.2650G>T
XM_024450641.1:c.2464G>T	XP_024306409.1:p.Gly822Cys
XM_024450642.1:c.2419G>T	XP_024306410.1:p.Gly807Cys
XM_024450643.1:c.2374G>T	XP_024306411.1:p.Gly792Cys
NM_001005862.3:c.2236G>T	NP_001005862.1:p.Gly746Cys
NM_001289936.2:c.2281G>T	NP_001276865.1:p.Gly761Cys
NM_001289937.2:c.2326G>T	NP_001276866.1:p.Gly776Cys
NM_001382782.1:c.2236G>T	NP_001369711.1:p.Gly746Cys
NM_001382783.1:c.2236G>T	NP_001369712.1:p.Gly746Cys
NM_001382784.1:c.2443G>T	NP_001369713.1:p.Gly815Cys
NM_001382785.1:c.2428G>T	NP_001369714.1:p.Gly810Cys
NM_001382786.1:c.2407G>T	NP_001369715.1:p.Gly803Cys
NM_001382787.1:c.2401G>T	NP_001369716.1:p.Gly801Cys
NM_001382788.1:c.2356G>T	NP_001369717.1:p.Gly786Cys
NM_001382789.1:c.2347G>T	NP_001369718.1:p.Gly783Cys
NM_001382790.1:c.2323G>T	NP_001369719.1:p.Gly775Cys
NM_001382791.1:c.2317G>T	NP_001369720.1:p.Gly773Cys
NM_001382792.1:c.2290G>T	NP_001369721.1:p.Gly764Cys
NM_001382793.1:c.2284G>T	NP_001369722.1:p.Gly762Cys
NM_001382794.1:c.2284G>T	NP_001369723.1:p.Gly762Cys
NM_001382795.1:c.2278G>T	NP_001369724.1:p.Gly760Cys
NM_001382796.1:c.2326G>T	NP_001369725.1:p.Gly776Cys
NM_001382797.1:c.2227G>T	NP_001369726.1:p.Gly743Cys
NM_001382798.1:c.2326G>T	NP_001369727.1:p.Gly776Cys
NM_001382799.1:c.2146G>T	NP_001369728.1:p.Gly716Cys
NM_001382800.1:c.2308-305G>T	NP_001369729.1:n.2308-305G>T
NM_001382801.1:c.2278G>T	NP_001369730.1:p.Gly760Cys
NM_001382802.1:c.2068G>T	NP_001369731.1:p.Gly690Cys
NM_001382803.1:c.2284G>T	NP_001369732.1:p.Gly762Cys
NM_001382804.1:c.1498G>T	NP_001369733.1:p.Gly500Cys
NM_001382805.1:c.2208+1084G>T	NP_001369734.1:n.2208+1084G>T
NM_001382806.1:c.1288G>T	NP_001369735.1:p.Gly430Cys
NM_004448.4:c.2326G>T MANE Select	NP_004439.2:p.Gly776Cys
NR_110535.2:n.2564G>T