Canonical Allele Identifier: CA399302888
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145848373

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724757C>G , CM000679.2:g.39724757C>G GRCh38
NC_000017.10:g.37881010C>G , CM000679.1:g.37881010C>G GRCh37
NC_000017.9:g.35134536C>G NCBI36
NG_007503.1:g.41618C>G , LRG_724:g.41618C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2339C>G MANE Select ENSP00000269571.4:p.Pro780Arg
ENST00000269571.9:c.2339C>G ENSP00000269571.4:p.Pro780Arg
ENST00000406381.6:c.2249C>G ENSP00000385185.2:p.Pro750Arg
ENST00000445658.6:c.1511C>G ENSP00000404047.2:p.Pro504Arg
ENST00000541774.5:c.2294C>G ENSP00000446466.1:p.Pro765Arg
ENST00000578373.5:c.*2129C>G ENSP00000463427.1:n.*2129C>G
ENST00000580074.1:c.445C>G
ENST00000583038.5:n.3473C>G
ENST00000584450.5:c.2339C>G ENSP00000463714.1:p.Pro780Arg
ENST00000584601.5:c.2249C>G ENSP00000462438.1:p.Pro750Arg
NM_001005862.2:c.2249C>G , LRG_724t1:c.2249C>G NP_001005862.1:p.Pro750Arg
NM_001289936.1:c.2294C>G , LRG_724t4:c.2294C>G NP_001276865.1:p.Pro765Arg
NM_001289937.1:c.2339C>G NP_001276866.1:p.Pro780Arg
NM_004448.3:c.2339C>G , LRG_724t2:c.2339C>G NP_004439.2:p.Pro780Arg
NR_110535.1:n.2663C>G
XM_024450641.1:c.2477C>G XP_024306409.1:p.Pro826Arg
XM_024450642.1:c.2432C>G XP_024306410.1:p.Pro811Arg
XM_024450643.1:c.2387C>G XP_024306411.1:p.Pro796Arg
NM_001005862.3:c.2249C>G NP_001005862.1:p.Pro750Arg
NM_001289936.2:c.2294C>G NP_001276865.1:p.Pro765Arg
NM_001289937.2:c.2339C>G NP_001276866.1:p.Pro780Arg
NM_001382782.1:c.2249C>G NP_001369711.1:p.Pro750Arg
NM_001382783.1:c.2249C>G NP_001369712.1:p.Pro750Arg
NM_001382784.1:c.2456C>G NP_001369713.1:p.Pro819Arg
NM_001382785.1:c.2441C>G NP_001369714.1:p.Pro814Arg
NM_001382786.1:c.2420C>G NP_001369715.1:p.Pro807Arg
NM_001382787.1:c.2414C>G NP_001369716.1:p.Pro805Arg
NM_001382788.1:c.2369C>G NP_001369717.1:p.Pro790Arg
NM_001382789.1:c.2360C>G NP_001369718.1:p.Pro787Arg
NM_001382790.1:c.2336C>G NP_001369719.1:p.Pro779Arg
NM_001382791.1:c.2330C>G NP_001369720.1:p.Pro777Arg
NM_001382792.1:c.2303C>G NP_001369721.1:p.Pro768Arg
NM_001382793.1:c.2297C>G NP_001369722.1:p.Pro766Arg
NM_001382794.1:c.2297C>G NP_001369723.1:p.Pro766Arg
NM_001382795.1:c.2291C>G NP_001369724.1:p.Pro764Arg
NM_001382796.1:c.2339C>G NP_001369725.1:p.Pro780Arg
NM_001382797.1:c.2240C>G NP_001369726.1:p.Pro747Arg
NM_001382798.1:c.2339C>G NP_001369727.1:p.Pro780Arg
NM_001382799.1:c.2159C>G NP_001369728.1:p.Pro720Arg
NM_001382800.1:c.2308-292C>G NP_001369729.1:n.2308-292C>G
NM_001382801.1:c.2291C>G NP_001369730.1:p.Pro764Arg
NM_001382802.1:c.2081C>G NP_001369731.1:p.Pro694Arg
NM_001382803.1:c.2297C>G NP_001369732.1:p.Pro766Arg
NM_001382804.1:c.1511C>G NP_001369733.1:p.Pro504Arg
NM_001382805.1:c.2208+1097C>G NP_001369734.1:n.2208+1097C>G
NM_001382806.1:c.1301C>G NP_001369735.1:p.Pro434Arg
NM_004448.4:c.2339C>G MANE Select NP_004439.2:p.Pro780Arg
NR_110535.2:n.2577C>G