Canonical Allele Identifier: CA399304365
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145863613

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725088G>A , CM000679.2:g.39725088G>A GRCh38
NC_000017.10:g.37881341G>A , CM000679.1:g.37881341G>A GRCh37
NC_000017.9:g.35134867G>A NCBI36
NG_007503.1:g.41949G>A , LRG_724:g.41949G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2533G>A MANE Select ENSP00000269571.4:p.Asp845Asn
ENST00000269571.9:c.2533G>A ENSP00000269571.4:p.Asp845Asn
ENST00000406381.6:c.2443G>A ENSP00000385185.2:p.Asp815Asn
ENST00000445658.6:c.1705G>A ENSP00000404047.2:p.Asp569Asn
ENST00000541774.5:c.2488G>A ENSP00000446466.1:p.Asp830Asn
ENST00000578373.5:c.*2323G>A ENSP00000463427.1:n.*2323G>A
ENST00000580074.1:c.639G>A
ENST00000583038.5:n.3667G>A
ENST00000584450.5:c.2533G>A ENSP00000463714.1:p.Asp845Asn
ENST00000584601.5:c.2443G>A ENSP00000462438.1:p.Asp815Asn
NM_001005862.2:c.2443G>A , LRG_724t1:c.2443G>A NP_001005862.1:p.Asp815Asn
NM_001289936.1:c.2488G>A , LRG_724t4:c.2488G>A NP_001276865.1:p.Asp830Asn
NM_001289937.1:c.2533G>A NP_001276866.1:p.Asp845Asn
NM_004448.3:c.2533G>A , LRG_724t2:c.2533G>A NP_004439.2:p.Asp845Asn
NR_110535.1:n.2857G>A
XM_024450641.1:c.2671G>A XP_024306409.1:p.Asp891Asn
XM_024450642.1:c.2626G>A XP_024306410.1:p.Asp876Asn
XM_024450643.1:c.2581G>A XP_024306411.1:p.Asp861Asn
NM_001005862.3:c.2443G>A NP_001005862.1:p.Asp815Asn
NM_001289936.2:c.2488G>A NP_001276865.1:p.Asp830Asn
NM_001289937.2:c.2533G>A NP_001276866.1:p.Asp845Asn
NM_001382782.1:c.2443G>A NP_001369711.1:p.Asp815Asn
NM_001382783.1:c.2443G>A NP_001369712.1:p.Asp815Asn
NM_001382784.1:c.2650G>A NP_001369713.1:p.Asp884Asn
NM_001382785.1:c.2635G>A NP_001369714.1:p.Asp879Asn
NM_001382786.1:c.2614G>A NP_001369715.1:p.Asp872Asn
NM_001382787.1:c.2608G>A NP_001369716.1:p.Asp870Asn
NM_001382788.1:c.2563G>A NP_001369717.1:p.Asp855Asn
NM_001382789.1:c.2554G>A NP_001369718.1:p.Asp852Asn
NM_001382790.1:c.2530G>A NP_001369719.1:p.Asp844Asn
NM_001382791.1:c.2524G>A NP_001369720.1:p.Asp842Asn
NM_001382792.1:c.2497G>A NP_001369721.1:p.Asp833Asn
NM_001382793.1:c.2491G>A NP_001369722.1:p.Asp831Asn
NM_001382794.1:c.2491G>A NP_001369723.1:p.Asp831Asn
NM_001382795.1:c.2485G>A NP_001369724.1:p.Asp829Asn
NM_001382796.1:c.2533G>A NP_001369725.1:p.Asp845Asn
NM_001382797.1:c.2434G>A NP_001369726.1:p.Asp812Asn
NM_001382798.1:c.2493+177G>A NP_001369727.1:n.2493+177G>A
NM_001382799.1:c.2353G>A NP_001369728.1:p.Asp785Asn
NM_001382800.1:c.2347G>A NP_001369729.1:p.Asp783Asn
NM_001382801.1:c.2445+177G>A NP_001369730.1:n.2445+177G>A
NM_001382802.1:c.2275G>A NP_001369731.1:p.Asp759Asn
NM_001382803.1:c.2491G>A NP_001369732.1:p.Asp831Asn
NM_001382804.1:c.1705G>A NP_001369733.1:p.Asp569Asn
NM_001382805.1:c.2208+1428G>A NP_001369734.1:n.2208+1428G>A
NM_001382806.1:c.1495G>A NP_001369735.1:p.Asp499Asn
NM_004448.4:c.2533G>A MANE Select NP_004439.2:p.Asp845Asn
NR_110535.2:n.2771G>A