Canonical Allele Identifier: CA399302928

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145848646
• MyVariant Identifiers: chr17:g.37881019C>A (hg19) ; chr17:g.39724766C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724766C>A , CM000679.2:g.39724766C>A	GRCh38
NC_000017.10:g.37881019C>A , CM000679.1:g.37881019C>A	GRCh37
NC_000017.9:g.35134545C>A	NCBI36
NG_007503.1:g.41627C>A , LRG_724:g.41627C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2348C>A MANE Select	ENSP00000269571.4:p.Ser783Tyr
ENST00000269571.9:c.2348C>A	ENSP00000269571.4:p.Ser783Tyr
ENST00000406381.6:c.2258C>A	ENSP00000385185.2:p.Ser753Tyr
ENST00000445658.6:c.1520C>A	ENSP00000404047.2:p.Ser507Tyr
ENST00000541774.5:c.2303C>A	ENSP00000446466.1:p.Ser768Tyr
ENST00000578373.5:c.*2138C>A	ENSP00000463427.1:n.*2138C>A
ENST00000580074.1:c.454C>A
ENST00000583038.5:n.3482C>A
ENST00000584450.5:c.2348C>A	ENSP00000463714.1:p.Ser783Tyr
ENST00000584601.5:c.2258C>A	ENSP00000462438.1:p.Ser753Tyr
NM_001005862.2:c.2258C>A , LRG_724t1:c.2258C>A	NP_001005862.1:p.Ser753Tyr
NM_001289936.1:c.2303C>A , LRG_724t4:c.2303C>A	NP_001276865.1:p.Ser768Tyr
NM_001289937.1:c.2348C>A	NP_001276866.1:p.Ser783Tyr
NM_004448.3:c.2348C>A , LRG_724t2:c.2348C>A	NP_004439.2:p.Ser783Tyr
NR_110535.1:n.2672C>A
XM_024450641.1:c.2486C>A	XP_024306409.1:p.Ser829Tyr
XM_024450642.1:c.2441C>A	XP_024306410.1:p.Ser814Tyr
XM_024450643.1:c.2396C>A	XP_024306411.1:p.Ser799Tyr
NM_001005862.3:c.2258C>A	NP_001005862.1:p.Ser753Tyr
NM_001289936.2:c.2303C>A	NP_001276865.1:p.Ser768Tyr
NM_001289937.2:c.2348C>A	NP_001276866.1:p.Ser783Tyr
NM_001382782.1:c.2258C>A	NP_001369711.1:p.Ser753Tyr
NM_001382783.1:c.2258C>A	NP_001369712.1:p.Ser753Tyr
NM_001382784.1:c.2465C>A	NP_001369713.1:p.Ser822Tyr
NM_001382785.1:c.2450C>A	NP_001369714.1:p.Ser817Tyr
NM_001382786.1:c.2429C>A	NP_001369715.1:p.Ser810Tyr
NM_001382787.1:c.2423C>A	NP_001369716.1:p.Ser808Tyr
NM_001382788.1:c.2378C>A	NP_001369717.1:p.Ser793Tyr
NM_001382789.1:c.2369C>A	NP_001369718.1:p.Ser790Tyr
NM_001382790.1:c.2345C>A	NP_001369719.1:p.Ser782Tyr
NM_001382791.1:c.2339C>A	NP_001369720.1:p.Ser780Tyr
NM_001382792.1:c.2312C>A	NP_001369721.1:p.Ser771Tyr
NM_001382793.1:c.2306C>A	NP_001369722.1:p.Ser769Tyr
NM_001382794.1:c.2306C>A	NP_001369723.1:p.Ser769Tyr
NM_001382795.1:c.2300C>A	NP_001369724.1:p.Ser767Tyr
NM_001382796.1:c.2348C>A	NP_001369725.1:p.Ser783Tyr
NM_001382797.1:c.2249C>A	NP_001369726.1:p.Ser750Tyr
NM_001382798.1:c.2348C>A	NP_001369727.1:p.Ser783Tyr
NM_001382799.1:c.2168C>A	NP_001369728.1:p.Ser723Tyr
NM_001382800.1:c.2308-283C>A	NP_001369729.1:n.2308-283C>A
NM_001382801.1:c.2300C>A	NP_001369730.1:p.Ser767Tyr
NM_001382802.1:c.2090C>A	NP_001369731.1:p.Ser697Tyr
NM_001382803.1:c.2306C>A	NP_001369732.1:p.Ser769Tyr
NM_001382804.1:c.1520C>A	NP_001369733.1:p.Ser507Tyr
NM_001382805.1:c.2208+1106C>A	NP_001369734.1:n.2208+1106C>A
NM_001382806.1:c.1310C>A	NP_001369735.1:p.Ser437Tyr
NM_004448.4:c.2348C>A MANE Select	NP_004439.2:p.Ser783Tyr
NR_110535.2:n.2586C>A