Canonical Allele Identifier: CA399303231
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145850372

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724810A>G , CM000679.2:g.39724810A>G GRCh38
NC_000017.10:g.37881063A>G , CM000679.1:g.37881063A>G GRCh37
NC_000017.9:g.35134589A>G NCBI36
NG_007503.1:g.41671A>G , LRG_724:g.41671A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2392A>G MANE Select ENSP00000269571.4:p.Thr798Ala
ENST00000269571.9:c.2392A>G ENSP00000269571.4:p.Thr798Ala
ENST00000406381.6:c.2302A>G ENSP00000385185.2:p.Thr768Ala
ENST00000445658.6:c.1564A>G ENSP00000404047.2:p.Thr522Ala
ENST00000541774.5:c.2347A>G ENSP00000446466.1:p.Thr783Ala
ENST00000578373.5:c.*2182A>G ENSP00000463427.1:n.*2182A>G
ENST00000580074.1:c.498A>G
ENST00000583038.5:n.3526A>G
ENST00000584450.5:c.2392A>G ENSP00000463714.1:p.Thr798Ala
ENST00000584601.5:c.2302A>G ENSP00000462438.1:p.Thr768Ala
NM_001005862.2:c.2302A>G , LRG_724t1:c.2302A>G NP_001005862.1:p.Thr768Ala
NM_001289936.1:c.2347A>G , LRG_724t4:c.2347A>G NP_001276865.1:p.Thr783Ala
NM_001289937.1:c.2392A>G NP_001276866.1:p.Thr798Ala
NM_004448.3:c.2392A>G , LRG_724t2:c.2392A>G NP_004439.2:p.Thr798Ala
NR_110535.1:n.2716A>G
XM_024450641.1:c.2530A>G XP_024306409.1:p.Thr844Ala
XM_024450642.1:c.2485A>G XP_024306410.1:p.Thr829Ala
XM_024450643.1:c.2440A>G XP_024306411.1:p.Thr814Ala
NM_001005862.3:c.2302A>G NP_001005862.1:p.Thr768Ala
NM_001289936.2:c.2347A>G NP_001276865.1:p.Thr783Ala
NM_001289937.2:c.2392A>G NP_001276866.1:p.Thr798Ala
NM_001382782.1:c.2302A>G NP_001369711.1:p.Thr768Ala
NM_001382783.1:c.2302A>G NP_001369712.1:p.Thr768Ala
NM_001382784.1:c.2509A>G NP_001369713.1:p.Thr837Ala
NM_001382785.1:c.2494A>G NP_001369714.1:p.Thr832Ala
NM_001382786.1:c.2473A>G NP_001369715.1:p.Thr825Ala
NM_001382787.1:c.2467A>G NP_001369716.1:p.Thr823Ala
NM_001382788.1:c.2422A>G NP_001369717.1:p.Thr808Ala
NM_001382789.1:c.2413A>G NP_001369718.1:p.Thr805Ala
NM_001382790.1:c.2389A>G NP_001369719.1:p.Thr797Ala
NM_001382791.1:c.2383A>G NP_001369720.1:p.Thr795Ala
NM_001382792.1:c.2356A>G NP_001369721.1:p.Thr786Ala
NM_001382793.1:c.2350A>G NP_001369722.1:p.Thr784Ala
NM_001382794.1:c.2350A>G NP_001369723.1:p.Thr784Ala
NM_001382795.1:c.2344A>G NP_001369724.1:p.Thr782Ala
NM_001382796.1:c.2392A>G NP_001369725.1:p.Thr798Ala
NM_001382797.1:c.2293A>G NP_001369726.1:p.Thr765Ala
NM_001382798.1:c.2392A>G NP_001369727.1:p.Thr798Ala
NM_001382799.1:c.2212A>G NP_001369728.1:p.Thr738Ala
NM_001382800.1:c.2308-239A>G NP_001369729.1:n.2308-239A>G
NM_001382801.1:c.2344A>G NP_001369730.1:p.Thr782Ala
NM_001382802.1:c.2134A>G NP_001369731.1:p.Thr712Ala
NM_001382803.1:c.2350A>G NP_001369732.1:p.Thr784Ala
NM_001382804.1:c.1564A>G NP_001369733.1:p.Thr522Ala
NM_001382805.1:c.2208+1150A>G NP_001369734.1:n.2208+1150A>G
NM_001382806.1:c.1354A>G NP_001369735.1:p.Thr452Ala
NM_004448.4:c.2392A>G MANE Select NP_004439.2:p.Thr798Ala
NR_110535.2:n.2630A>G