Canonical Allele Identifier: CA399304452
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs776236294

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725105C>G , CM000679.2:g.39725105C>G GRCh38
NC_000017.10:g.37881358C>G , CM000679.1:g.37881358C>G GRCh37
NC_000017.9:g.35134884C>G NCBI36
NG_007503.1:g.41966C>G , LRG_724:g.41966C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2550C>G MANE Select ENSP00000269571.4:p.Asn850Lys
ENST00000269571.9:c.2550C>G ENSP00000269571.4:p.Asn850Lys
ENST00000406381.6:c.2460C>G ENSP00000385185.2:p.Asn820Lys
ENST00000445658.6:c.1722C>G ENSP00000404047.2:p.Asn574Lys
ENST00000541774.5:c.2505C>G ENSP00000446466.1:p.Asn835Lys
ENST00000578373.5:c.*2340C>G ENSP00000463427.1:n.*2340C>G
ENST00000580074.1:c.656C>G
ENST00000583038.5:n.3684C>G
ENST00000584450.5:c.2550C>G ENSP00000463714.1:p.Asn850Lys
ENST00000584601.5:c.2460C>G ENSP00000462438.1:p.Asn820Lys
NM_001005862.2:c.2460C>G , LRG_724t1:c.2460C>G NP_001005862.1:p.Asn820Lys
NM_001289936.1:c.2505C>G , LRG_724t4:c.2505C>G NP_001276865.1:p.Asn835Lys
NM_001289937.1:c.2550C>G NP_001276866.1:p.Asn850Lys
NM_004448.3:c.2550C>G , LRG_724t2:c.2550C>G NP_004439.2:p.Asn850Lys
NR_110535.1:n.2874C>G
XM_024450641.1:c.2688C>G XP_024306409.1:p.Asn896Lys
XM_024450642.1:c.2643C>G XP_024306410.1:p.Asn881Lys
XM_024450643.1:c.2598C>G XP_024306411.1:p.Asn866Lys
NM_001005862.3:c.2460C>G NP_001005862.1:p.Asn820Lys
NM_001289936.2:c.2505C>G NP_001276865.1:p.Asn835Lys
NM_001289937.2:c.2550C>G NP_001276866.1:p.Asn850Lys
NM_001382782.1:c.2460C>G NP_001369711.1:p.Asn820Lys
NM_001382783.1:c.2460C>G NP_001369712.1:p.Asn820Lys
NM_001382784.1:c.2667C>G NP_001369713.1:p.Asn889Lys
NM_001382785.1:c.2652C>G NP_001369714.1:p.Asn884Lys
NM_001382786.1:c.2631C>G NP_001369715.1:p.Asn877Lys
NM_001382787.1:c.2625C>G NP_001369716.1:p.Asn875Lys
NM_001382788.1:c.2580C>G NP_001369717.1:p.Asn860Lys
NM_001382789.1:c.2571C>G NP_001369718.1:p.Asn857Lys
NM_001382790.1:c.2547C>G NP_001369719.1:p.Asn849Lys
NM_001382791.1:c.2541C>G NP_001369720.1:p.Asn847Lys
NM_001382792.1:c.2514C>G NP_001369721.1:p.Asn838Lys
NM_001382793.1:c.2508C>G NP_001369722.1:p.Asn836Lys
NM_001382794.1:c.2508C>G NP_001369723.1:p.Asn836Lys
NM_001382795.1:c.2502C>G NP_001369724.1:p.Asn834Lys
NM_001382796.1:c.2550C>G NP_001369725.1:p.Asn850Lys
NM_001382797.1:c.2451C>G NP_001369726.1:p.Asn817Lys
NM_001382798.1:c.2493+194C>G NP_001369727.1:n.2493+194C>G
NM_001382799.1:c.2370C>G NP_001369728.1:p.Asn790Lys
NM_001382800.1:c.2364C>G NP_001369729.1:p.Asn788Lys
NM_001382801.1:c.2445+194C>G NP_001369730.1:n.2445+194C>G
NM_001382802.1:c.2292C>G NP_001369731.1:p.Asn764Lys
NM_001382803.1:c.2508C>G NP_001369732.1:p.Asn836Lys
NM_001382804.1:c.1722C>G NP_001369733.1:p.Asn574Lys
NM_001382805.1:c.2208+1445C>G NP_001369734.1:n.2208+1445C>G
NM_001382806.1:c.1512C>G NP_001369735.1:p.Asn504Lys
NM_004448.4:c.2550C>G MANE Select NP_004439.2:p.Asn850Lys
NR_110535.2:n.2788C>G