Canonical Allele Identifier: CA399302840

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145847414
• MyVariant Identifiers: chr17:g.37880995C>A (hg19) ; chr17:g.39724742C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724742C>A , CM000679.2:g.39724742C>A	GRCh38
NC_000017.10:g.37880995C>A , CM000679.1:g.37880995C>A	GRCh37
NC_000017.9:g.35134521C>A	NCBI36
NG_007503.1:g.41603C>A , LRG_724:g.41603C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2324C>A MANE Select	ENSP00000269571.4:p.Ala775Asp
ENST00000269571.9:c.2324C>A	ENSP00000269571.4:p.Ala775Asp
ENST00000406381.6:c.2234C>A	ENSP00000385185.2:p.Ala745Asp
ENST00000445658.6:c.1496C>A	ENSP00000404047.2:p.Ala499Asp
ENST00000541774.5:c.2279C>A	ENSP00000446466.1:p.Ala760Asp
ENST00000578373.5:c.*2114C>A	ENSP00000463427.1:n.*2114C>A
ENST00000580074.1:c.430C>A
ENST00000583038.5:n.3458C>A
ENST00000584450.5:c.2324C>A	ENSP00000463714.1:p.Ala775Asp
ENST00000584601.5:c.2234C>A	ENSP00000462438.1:p.Ala745Asp
NM_001005862.2:c.2234C>A , LRG_724t1:c.2234C>A	NP_001005862.1:p.Ala745Asp
NM_001289936.1:c.2279C>A , LRG_724t4:c.2279C>A	NP_001276865.1:p.Ala760Asp
NM_001289937.1:c.2324C>A	NP_001276866.1:p.Ala775Asp
NM_004448.3:c.2324C>A , LRG_724t2:c.2324C>A	NP_004439.2:p.Ala775Asp
NR_110535.1:n.2648C>A
XM_024450641.1:c.2462C>A	XP_024306409.1:p.Ala821Asp
XM_024450642.1:c.2417C>A	XP_024306410.1:p.Ala806Asp
XM_024450643.1:c.2372C>A	XP_024306411.1:p.Ala791Asp
NM_001005862.3:c.2234C>A	NP_001005862.1:p.Ala745Asp
NM_001289936.2:c.2279C>A	NP_001276865.1:p.Ala760Asp
NM_001289937.2:c.2324C>A	NP_001276866.1:p.Ala775Asp
NM_001382782.1:c.2234C>A	NP_001369711.1:p.Ala745Asp
NM_001382783.1:c.2234C>A	NP_001369712.1:p.Ala745Asp
NM_001382784.1:c.2441C>A	NP_001369713.1:p.Ala814Asp
NM_001382785.1:c.2426C>A	NP_001369714.1:p.Ala809Asp
NM_001382786.1:c.2405C>A	NP_001369715.1:p.Ala802Asp
NM_001382787.1:c.2399C>A	NP_001369716.1:p.Ala800Asp
NM_001382788.1:c.2354C>A	NP_001369717.1:p.Ala785Asp
NM_001382789.1:c.2345C>A	NP_001369718.1:p.Ala782Asp
NM_001382790.1:c.2321C>A	NP_001369719.1:p.Ala774Asp
NM_001382791.1:c.2315C>A	NP_001369720.1:p.Ala772Asp
NM_001382792.1:c.2288C>A	NP_001369721.1:p.Ala763Asp
NM_001382793.1:c.2282C>A	NP_001369722.1:p.Ala761Asp
NM_001382794.1:c.2282C>A	NP_001369723.1:p.Ala761Asp
NM_001382795.1:c.2276C>A	NP_001369724.1:p.Ala759Asp
NM_001382796.1:c.2324C>A	NP_001369725.1:p.Ala775Asp
NM_001382797.1:c.2225C>A	NP_001369726.1:p.Ala742Asp
NM_001382798.1:c.2324C>A	NP_001369727.1:p.Ala775Asp
NM_001382799.1:c.2144C>A	NP_001369728.1:p.Ala715Asp
NM_001382800.1:c.2308-307C>A	NP_001369729.1:n.2308-307C>A
NM_001382801.1:c.2276C>A	NP_001369730.1:p.Ala759Asp
NM_001382802.1:c.2066C>A	NP_001369731.1:p.Ala689Asp
NM_001382803.1:c.2282C>A	NP_001369732.1:p.Ala761Asp
NM_001382804.1:c.1496C>A	NP_001369733.1:p.Ala499Asp
NM_001382805.1:c.2208+1082C>A	NP_001369734.1:n.2208+1082C>A
NM_001382806.1:c.1286C>A	NP_001369735.1:p.Ala429Asp
NM_004448.4:c.2324C>A MANE Select	NP_004439.2:p.Ala775Asp
NR_110535.2:n.2562C>A