Canonical Allele Identifier: CA2259228015
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724817T= , CM000679.2:g.39724817T= GRCh38
NC_000017.10:g.37881070T= , CM000679.1:g.37881070T= GRCh37
NC_000017.9:g.35134596T= NCBI36
NG_007503.1:g.41678T= , LRG_724:g.41678T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2399T= MANE Select ENSP00000269571.4:p.Leu800=
ENST00000269571.9:c.2399T= ENSP00000269571.4:p.Leu800=
ENST00000406381.6:c.2309T= ENSP00000385185.2:p.Leu770=
ENST00000445658.6:c.1571T= ENSP00000404047.2:p.Leu524=
ENST00000541774.5:c.2354T= ENSP00000446466.1:p.Leu785=
ENST00000578373.5:c.*2189T= ENSP00000463427.1:n.*2189T=
ENST00000580074.1:c.505T=
ENST00000583038.5:n.3533T=
ENST00000584450.5:c.2399T= ENSP00000463714.1:p.Leu800=
ENST00000584601.5:c.2309T= ENSP00000462438.1:p.Leu770=
NM_001005862.2:c.2309T= , LRG_724t1:c.2309T= NP_001005862.1:p.Leu770=
NM_001289936.1:c.2354T= , LRG_724t4:c.2354T= NP_001276865.1:p.Leu785=
NM_001289937.1:c.2399T= NP_001276866.1:p.Leu800=
NM_004448.3:c.2399T= , LRG_724t2:c.2399T= NP_004439.2:p.Leu800=
NR_110535.1:n.2723T=
XM_024450641.1:c.2537T= XP_024306409.1:p.Leu846=
XM_024450642.1:c.2492T= XP_024306410.1:p.Leu831=
XM_024450643.1:c.2447T= XP_024306411.1:p.Leu816=
NM_001005862.3:c.2309T= NP_001005862.1:p.Leu770=
NM_001289936.2:c.2354T= NP_001276865.1:p.Leu785=
NM_001289937.2:c.2399T= NP_001276866.1:p.Leu800=
NM_001382782.1:c.2309T= NP_001369711.1:p.Leu770=
NM_001382783.1:c.2309T= NP_001369712.1:p.Leu770=
NM_001382784.1:c.2516T= NP_001369713.1:p.Leu839=
NM_001382785.1:c.2501T= NP_001369714.1:p.Leu834=
NM_001382786.1:c.2480T= NP_001369715.1:p.Leu827=
NM_001382787.1:c.2474T= NP_001369716.1:p.Leu825=
NM_001382788.1:c.2429T= NP_001369717.1:p.Leu810=
NM_001382789.1:c.2420T= NP_001369718.1:p.Leu807=
NM_001382790.1:c.2396T= NP_001369719.1:p.Leu799=
NM_001382791.1:c.2390T= NP_001369720.1:p.Leu797=
NM_001382792.1:c.2363T= NP_001369721.1:p.Leu788=
NM_001382793.1:c.2357T= NP_001369722.1:p.Leu786=
NM_001382794.1:c.2357T= NP_001369723.1:p.Leu786=
NM_001382795.1:c.2351T= NP_001369724.1:p.Leu784=
NM_001382796.1:c.2399T= NP_001369725.1:p.Leu800=
NM_001382797.1:c.2300T= NP_001369726.1:p.Leu767=
NM_001382798.1:c.2399T= NP_001369727.1:p.Leu800=
NM_001382799.1:c.2219T= NP_001369728.1:p.Leu740=
NM_001382800.1:c.2308-232T= NP_001369729.1:n.2308-232T=
NM_001382801.1:c.2351T= NP_001369730.1:p.Leu784=
NM_001382802.1:c.2141T= NP_001369731.1:p.Leu714=
NM_001382803.1:c.2357T= NP_001369732.1:p.Leu786=
NM_001382804.1:c.1571T= NP_001369733.1:p.Leu524=
NM_001382805.1:c.2208+1157T= NP_001369734.1:n.2208+1157T=
NM_001382806.1:c.1361T= NP_001369735.1:p.Leu454=
NM_004448.4:c.2399T= MANE Select NP_004439.2:p.Leu800=
NR_110535.2:n.2637T=