Canonical Allele Identifier: CA399302872
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145848092

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724751G>C , CM000679.2:g.39724751G>C GRCh38
NC_000017.10:g.37881004G>C , CM000679.1:g.37881004G>C GRCh37
NC_000017.9:g.35134530G>C NCBI36
NG_007503.1:g.41612G>C , LRG_724:g.41612G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2333G>C MANE Select ENSP00000269571.4:p.Gly778Ala
ENST00000269571.9:c.2333G>C ENSP00000269571.4:p.Gly778Ala
ENST00000406381.6:c.2243G>C ENSP00000385185.2:p.Gly748Ala
ENST00000445658.6:c.1505G>C ENSP00000404047.2:p.Gly502Ala
ENST00000541774.5:c.2288G>C ENSP00000446466.1:p.Gly763Ala
ENST00000578373.5:c.*2123G>C ENSP00000463427.1:n.*2123G>C
ENST00000580074.1:c.439G>C
ENST00000583038.5:n.3467G>C
ENST00000584450.5:c.2333G>C ENSP00000463714.1:p.Gly778Ala
ENST00000584601.5:c.2243G>C ENSP00000462438.1:p.Gly748Ala
NM_001005862.2:c.2243G>C , LRG_724t1:c.2243G>C NP_001005862.1:p.Gly748Ala
NM_001289936.1:c.2288G>C , LRG_724t4:c.2288G>C NP_001276865.1:p.Gly763Ala
NM_001289937.1:c.2333G>C NP_001276866.1:p.Gly778Ala
NM_004448.3:c.2333G>C , LRG_724t2:c.2333G>C NP_004439.2:p.Gly778Ala
NR_110535.1:n.2657G>C
XM_024450641.1:c.2471G>C XP_024306409.1:p.Gly824Ala
XM_024450642.1:c.2426G>C XP_024306410.1:p.Gly809Ala
XM_024450643.1:c.2381G>C XP_024306411.1:p.Gly794Ala
NM_001005862.3:c.2243G>C NP_001005862.1:p.Gly748Ala
NM_001289936.2:c.2288G>C NP_001276865.1:p.Gly763Ala
NM_001289937.2:c.2333G>C NP_001276866.1:p.Gly778Ala
NM_001382782.1:c.2243G>C NP_001369711.1:p.Gly748Ala
NM_001382783.1:c.2243G>C NP_001369712.1:p.Gly748Ala
NM_001382784.1:c.2450G>C NP_001369713.1:p.Gly817Ala
NM_001382785.1:c.2435G>C NP_001369714.1:p.Gly812Ala
NM_001382786.1:c.2414G>C NP_001369715.1:p.Gly805Ala
NM_001382787.1:c.2408G>C NP_001369716.1:p.Gly803Ala
NM_001382788.1:c.2363G>C NP_001369717.1:p.Gly788Ala
NM_001382789.1:c.2354G>C NP_001369718.1:p.Gly785Ala
NM_001382790.1:c.2330G>C NP_001369719.1:p.Gly777Ala
NM_001382791.1:c.2324G>C NP_001369720.1:p.Gly775Ala
NM_001382792.1:c.2297G>C NP_001369721.1:p.Gly766Ala
NM_001382793.1:c.2291G>C NP_001369722.1:p.Gly764Ala
NM_001382794.1:c.2291G>C NP_001369723.1:p.Gly764Ala
NM_001382795.1:c.2285G>C NP_001369724.1:p.Gly762Ala
NM_001382796.1:c.2333G>C NP_001369725.1:p.Gly778Ala
NM_001382797.1:c.2234G>C NP_001369726.1:p.Gly745Ala
NM_001382798.1:c.2333G>C NP_001369727.1:p.Gly778Ala
NM_001382799.1:c.2153G>C NP_001369728.1:p.Gly718Ala
NM_001382800.1:c.2308-298G>C NP_001369729.1:n.2308-298G>C
NM_001382801.1:c.2285G>C NP_001369730.1:p.Gly762Ala
NM_001382802.1:c.2075G>C NP_001369731.1:p.Gly692Ala
NM_001382803.1:c.2291G>C NP_001369732.1:p.Gly764Ala
NM_001382804.1:c.1505G>C NP_001369733.1:p.Gly502Ala
NM_001382805.1:c.2208+1091G>C NP_001369734.1:n.2208+1091G>C
NM_001382806.1:c.1295G>C NP_001369735.1:p.Gly432Ala
NM_004448.4:c.2333G>C MANE Select NP_004439.2:p.Gly778Ala
NR_110535.2:n.2571G>C