Canonical Allele Identifier: CA399303123

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849678
• MyVariant Identifiers: chr17:g.37881046C>A (hg19) ; chr17:g.39724793C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724793C>A , CM000679.2:g.39724793C>A	GRCh38
NC_000017.10:g.37881046C>A , CM000679.1:g.37881046C>A	GRCh37
NC_000017.9:g.35134572C>A	NCBI36
NG_007503.1:g.41654C>A , LRG_724:g.41654C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2375C>A MANE Select	ENSP00000269571.4:p.Ser792Tyr
ENST00000269571.9:c.2375C>A	ENSP00000269571.4:p.Ser792Tyr
ENST00000406381.6:c.2285C>A	ENSP00000385185.2:p.Ser762Tyr
ENST00000445658.6:c.1547C>A	ENSP00000404047.2:p.Ser516Tyr
ENST00000541774.5:c.2330C>A	ENSP00000446466.1:p.Ser777Tyr
ENST00000578373.5:c.*2165C>A	ENSP00000463427.1:n.*2165C>A
ENST00000580074.1:c.481C>A
ENST00000583038.5:n.3509C>A
ENST00000584450.5:c.2375C>A	ENSP00000463714.1:p.Ser792Tyr
ENST00000584601.5:c.2285C>A	ENSP00000462438.1:p.Ser762Tyr
NM_001005862.2:c.2285C>A , LRG_724t1:c.2285C>A	NP_001005862.1:p.Ser762Tyr
NM_001289936.1:c.2330C>A , LRG_724t4:c.2330C>A	NP_001276865.1:p.Ser777Tyr
NM_001289937.1:c.2375C>A	NP_001276866.1:p.Ser792Tyr
NM_004448.3:c.2375C>A , LRG_724t2:c.2375C>A	NP_004439.2:p.Ser792Tyr
NR_110535.1:n.2699C>A
XM_024450641.1:c.2513C>A	XP_024306409.1:p.Ser838Tyr
XM_024450642.1:c.2468C>A	XP_024306410.1:p.Ser823Tyr
XM_024450643.1:c.2423C>A	XP_024306411.1:p.Ser808Tyr
NM_001005862.3:c.2285C>A	NP_001005862.1:p.Ser762Tyr
NM_001289936.2:c.2330C>A	NP_001276865.1:p.Ser777Tyr
NM_001289937.2:c.2375C>A	NP_001276866.1:p.Ser792Tyr
NM_001382782.1:c.2285C>A	NP_001369711.1:p.Ser762Tyr
NM_001382783.1:c.2285C>A	NP_001369712.1:p.Ser762Tyr
NM_001382784.1:c.2492C>A	NP_001369713.1:p.Ser831Tyr
NM_001382785.1:c.2477C>A	NP_001369714.1:p.Ser826Tyr
NM_001382786.1:c.2456C>A	NP_001369715.1:p.Ser819Tyr
NM_001382787.1:c.2450C>A	NP_001369716.1:p.Ser817Tyr
NM_001382788.1:c.2405C>A	NP_001369717.1:p.Ser802Tyr
NM_001382789.1:c.2396C>A	NP_001369718.1:p.Ser799Tyr
NM_001382790.1:c.2372C>A	NP_001369719.1:p.Ser791Tyr
NM_001382791.1:c.2366C>A	NP_001369720.1:p.Ser789Tyr
NM_001382792.1:c.2339C>A	NP_001369721.1:p.Ser780Tyr
NM_001382793.1:c.2333C>A	NP_001369722.1:p.Ser778Tyr
NM_001382794.1:c.2333C>A	NP_001369723.1:p.Ser778Tyr
NM_001382795.1:c.2327C>A	NP_001369724.1:p.Ser776Tyr
NM_001382796.1:c.2375C>A	NP_001369725.1:p.Ser792Tyr
NM_001382797.1:c.2276C>A	NP_001369726.1:p.Ser759Tyr
NM_001382798.1:c.2375C>A	NP_001369727.1:p.Ser792Tyr
NM_001382799.1:c.2195C>A	NP_001369728.1:p.Ser732Tyr
NM_001382800.1:c.2308-256C>A	NP_001369729.1:n.2308-256C>A
NM_001382801.1:c.2327C>A	NP_001369730.1:p.Ser776Tyr
NM_001382802.1:c.2117C>A	NP_001369731.1:p.Ser706Tyr
NM_001382803.1:c.2333C>A	NP_001369732.1:p.Ser778Tyr
NM_001382804.1:c.1547C>A	NP_001369733.1:p.Ser516Tyr
NM_001382805.1:c.2208+1133C>A	NP_001369734.1:n.2208+1133C>A
NM_001382806.1:c.1337C>A	NP_001369735.1:p.Ser446Tyr
NM_004448.4:c.2375C>A MANE Select	NP_004439.2:p.Ser792Tyr
NR_110535.2:n.2613C>A