Canonical Allele Identifier: CA2259227975
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724733A= , CM000679.2:g.39724733A= GRCh38
NC_000017.10:g.37880986A= , CM000679.1:g.37880986A= GRCh37
NC_000017.9:g.35134512A= NCBI36
NG_007503.1:g.41594A= , LRG_724:g.41594A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2315A= MANE Select ENSP00000269571.4:p.Tyr772=
ENST00000269571.9:c.2315A= ENSP00000269571.4:p.Tyr772=
ENST00000406381.6:c.2225A= ENSP00000385185.2:p.Tyr742=
ENST00000445658.6:c.1487A= ENSP00000404047.2:p.Tyr496=
ENST00000541774.5:c.2270A= ENSP00000446466.1:p.Tyr757=
ENST00000578373.5:c.*2105A= ENSP00000463427.1:n.*2105A=
ENST00000580074.1:c.421A=
ENST00000583038.5:n.3449A=
ENST00000584450.5:c.2315A= ENSP00000463714.1:p.Tyr772=
ENST00000584601.5:c.2225A= ENSP00000462438.1:p.Tyr742=
NM_001005862.2:c.2225A= , LRG_724t1:c.2225A= NP_001005862.1:p.Tyr742=
NM_001289936.1:c.2270A= , LRG_724t4:c.2270A= NP_001276865.1:p.Tyr757=
NM_001289937.1:c.2315A= NP_001276866.1:p.Tyr772=
NM_004448.3:c.2315A= , LRG_724t2:c.2315A= NP_004439.2:p.Tyr772=
NR_110535.1:n.2639A=
XM_024450641.1:c.2453A= XP_024306409.1:p.Tyr818=
XM_024450642.1:c.2408A= XP_024306410.1:p.Tyr803=
XM_024450643.1:c.2363A= XP_024306411.1:p.Tyr788=
NM_001005862.3:c.2225A= NP_001005862.1:p.Tyr742=
NM_001289936.2:c.2270A= NP_001276865.1:p.Tyr757=
NM_001289937.2:c.2315A= NP_001276866.1:p.Tyr772=
NM_001382782.1:c.2225A= NP_001369711.1:p.Tyr742=
NM_001382783.1:c.2225A= NP_001369712.1:p.Tyr742=
NM_001382784.1:c.2432A= NP_001369713.1:p.Tyr811=
NM_001382785.1:c.2417A= NP_001369714.1:p.Tyr806=
NM_001382786.1:c.2396A= NP_001369715.1:p.Tyr799=
NM_001382787.1:c.2390A= NP_001369716.1:p.Tyr797=
NM_001382788.1:c.2345A= NP_001369717.1:p.Tyr782=
NM_001382789.1:c.2336A= NP_001369718.1:p.Tyr779=
NM_001382790.1:c.2312A= NP_001369719.1:p.Tyr771=
NM_001382791.1:c.2306A= NP_001369720.1:p.Tyr769=
NM_001382792.1:c.2279A= NP_001369721.1:p.Tyr760=
NM_001382793.1:c.2273A= NP_001369722.1:p.Tyr758=
NM_001382794.1:c.2273A= NP_001369723.1:p.Tyr758=
NM_001382795.1:c.2267A= NP_001369724.1:p.Tyr756=
NM_001382796.1:c.2315A= NP_001369725.1:p.Tyr772=
NM_001382797.1:c.2216A= NP_001369726.1:p.Tyr739=
NM_001382798.1:c.2315A= NP_001369727.1:p.Tyr772=
NM_001382799.1:c.2135A= NP_001369728.1:p.Tyr712=
NM_001382800.1:c.2308-316A= NP_001369729.1:n.2308-316A=
NM_001382801.1:c.2267A= NP_001369730.1:p.Tyr756=
NM_001382802.1:c.2057A= NP_001369731.1:p.Tyr686=
NM_001382803.1:c.2273A= NP_001369732.1:p.Tyr758=
NM_001382804.1:c.1487A= NP_001369733.1:p.Tyr496=
NM_001382805.1:c.2208+1073A= NP_001369734.1:n.2208+1073A=
NM_001382806.1:c.1277A= NP_001369735.1:p.Tyr426=
NM_004448.4:c.2315A= MANE Select NP_004439.2:p.Tyr772=
NR_110535.2:n.2553A=