Canonical Allele Identifier: CA399303395
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724835T>G , CM000679.2:g.39724835T>G GRCh38
NC_000017.10:g.37881088T>G , CM000679.1:g.37881088T>G GRCh37
NC_000017.9:g.35134614T>G NCBI36
NG_007503.1:g.41696T>G , LRG_724:g.41696T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2417T>G MANE Select ENSP00000269571.4:p.Leu806Arg
ENST00000269571.9:c.2417T>G ENSP00000269571.4:p.Leu806Arg
ENST00000406381.6:c.2327T>G ENSP00000385185.2:p.Leu776Arg
ENST00000445658.6:c.1589T>G ENSP00000404047.2:p.Leu530Arg
ENST00000541774.5:c.2372T>G ENSP00000446466.1:p.Leu791Arg
ENST00000578373.5:c.*2207T>G ENSP00000463427.1:n.*2207T>G
ENST00000580074.1:c.523T>G
ENST00000583038.5:n.3551T>G
ENST00000584450.5:c.2417T>G ENSP00000463714.1:p.Leu806Arg
ENST00000584601.5:c.2327T>G ENSP00000462438.1:p.Leu776Arg
NM_001005862.2:c.2327T>G , LRG_724t1:c.2327T>G NP_001005862.1:p.Leu776Arg
NM_001289936.1:c.2372T>G , LRG_724t4:c.2372T>G NP_001276865.1:p.Leu791Arg
NM_001289937.1:c.2417T>G NP_001276866.1:p.Leu806Arg
NM_004448.3:c.2417T>G , LRG_724t2:c.2417T>G NP_004439.2:p.Leu806Arg
NR_110535.1:n.2741T>G
XM_024450641.1:c.2555T>G XP_024306409.1:p.Leu852Arg
XM_024450642.1:c.2510T>G XP_024306410.1:p.Leu837Arg
XM_024450643.1:c.2465T>G XP_024306411.1:p.Leu822Arg
NM_001005862.3:c.2327T>G NP_001005862.1:p.Leu776Arg
NM_001289936.2:c.2372T>G NP_001276865.1:p.Leu791Arg
NM_001289937.2:c.2417T>G NP_001276866.1:p.Leu806Arg
NM_001382782.1:c.2327T>G NP_001369711.1:p.Leu776Arg
NM_001382783.1:c.2327T>G NP_001369712.1:p.Leu776Arg
NM_001382784.1:c.2534T>G NP_001369713.1:p.Leu845Arg
NM_001382785.1:c.2519T>G NP_001369714.1:p.Leu840Arg
NM_001382786.1:c.2498T>G NP_001369715.1:p.Leu833Arg
NM_001382787.1:c.2492T>G NP_001369716.1:p.Leu831Arg
NM_001382788.1:c.2447T>G NP_001369717.1:p.Leu816Arg
NM_001382789.1:c.2438T>G NP_001369718.1:p.Leu813Arg
NM_001382790.1:c.2414T>G NP_001369719.1:p.Leu805Arg
NM_001382791.1:c.2408T>G NP_001369720.1:p.Leu803Arg
NM_001382792.1:c.2381T>G NP_001369721.1:p.Leu794Arg
NM_001382793.1:c.2375T>G NP_001369722.1:p.Leu792Arg
NM_001382794.1:c.2375T>G NP_001369723.1:p.Leu792Arg
NM_001382795.1:c.2369T>G NP_001369724.1:p.Leu790Arg
NM_001382796.1:c.2417T>G NP_001369725.1:p.Leu806Arg
NM_001382797.1:c.2318T>G NP_001369726.1:p.Leu773Arg
NM_001382798.1:c.2417T>G NP_001369727.1:p.Leu806Arg
NM_001382799.1:c.2237T>G NP_001369728.1:p.Leu746Arg
NM_001382800.1:c.2308-214T>G NP_001369729.1:n.2308-214T>G
NM_001382801.1:c.2369T>G NP_001369730.1:p.Leu790Arg
NM_001382802.1:c.2159T>G NP_001369731.1:p.Leu720Arg
NM_001382803.1:c.2375T>G NP_001369732.1:p.Leu792Arg
NM_001382804.1:c.1589T>G NP_001369733.1:p.Leu530Arg
NM_001382805.1:c.2208+1175T>G NP_001369734.1:n.2208+1175T>G
NM_001382806.1:c.1379T>G NP_001369735.1:p.Leu460Arg
NM_004448.4:c.2417T>G MANE Select NP_004439.2:p.Leu806Arg
NR_110535.2:n.2655T>G