Canonical Allele Identifier: CA399313585
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727837T>A , CM000679.2:g.39727837T>A GRCh38
NC_000017.10:g.37884090T>A , CM000679.1:g.37884090T>A GRCh37
NC_000017.9:g.35137616T>A NCBI36
NG_007503.1:g.44698T>A , LRG_724:g.44698T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3561T>A MANE Select ENSP00000269571.4:p.Phe1187Leu
ENST00000269571.9:c.3561T>A ENSP00000269571.4:p.Phe1187Leu
ENST00000406381.6:c.3471T>A ENSP00000385185.2:p.Phe1157Leu
ENST00000445658.6:c.2733T>A ENSP00000404047.2:p.Phe911Leu
ENST00000541774.5:c.3516T>A ENSP00000446466.1:p.Phe1172Leu
ENST00000578373.5:c.*3351T>A ENSP00000463427.1:n.*3351T>A
ENST00000584450.5:c.*140T>A ENSP00000463714.1:n.*140T>A
ENST00000584601.5:c.3471T>A ENSP00000462438.1:p.Phe1157Leu
NM_001005862.2:c.3471T>A , LRG_724t1:c.3471T>A NP_001005862.1:p.Phe1157Leu
NM_001289936.1:c.3516T>A , LRG_724t4:c.3516T>A NP_001276865.1:p.Phe1172Leu
NM_001289937.1:c.*140T>A NP_001276866.1:n.*140T>A
NM_004448.3:c.3561T>A , LRG_724t2:c.3561T>A NP_004439.2:p.Phe1187Leu
NR_110535.1:n.3885T>A
XM_024450641.1:c.3699T>A XP_024306409.1:p.Phe1233Leu
XM_024450642.1:c.3654T>A XP_024306410.1:p.Phe1218Leu
XM_024450643.1:c.3609T>A XP_024306411.1:p.Phe1203Leu
NM_001005862.3:c.3471T>A NP_001005862.1:p.Phe1157Leu
NM_001289936.2:c.3516T>A NP_001276865.1:p.Phe1172Leu
NM_001289937.2:c.*140T>A NP_001276866.1:n.*140T>A
NM_001382782.1:c.3471T>A NP_001369711.1:p.Phe1157Leu
NM_001382783.1:c.3471T>A NP_001369712.1:p.Phe1157Leu
NM_001382784.1:c.3678T>A NP_001369713.1:p.Phe1226Leu
NM_001382785.1:c.3663T>A NP_001369714.1:p.Phe1221Leu
NM_001382786.1:c.3642T>A NP_001369715.1:p.Phe1214Leu
NM_001382787.1:c.3636T>A NP_001369716.1:p.Phe1212Leu
NM_001382788.1:c.3591T>A NP_001369717.1:p.Phe1197Leu
NM_001382789.1:c.3582T>A NP_001369718.1:p.Phe1194Leu
NM_001382790.1:c.3558T>A NP_001369719.1:p.Phe1186Leu
NM_001382791.1:c.3552T>A NP_001369720.1:p.Phe1184Leu
NM_001382792.1:c.3525T>A NP_001369721.1:p.Phe1175Leu
NM_001382793.1:c.3519T>A NP_001369722.1:p.Phe1173Leu
NM_001382794.1:c.3519T>A NP_001369723.1:p.Phe1173Leu
NM_001382795.1:c.3513T>A NP_001369724.1:p.Phe1171Leu
NM_001382796.1:c.3474T>A NP_001369725.1:p.Phe1158Leu
NM_001382797.1:c.3462T>A NP_001369726.1:p.Phe1154Leu
NM_001382798.1:c.3405T>A NP_001369727.1:p.Phe1135Leu
NM_001382799.1:c.3381T>A NP_001369728.1:p.Phe1127Leu
NM_001382800.1:c.3375T>A NP_001369729.1:p.Phe1125Leu
NM_001382801.1:c.3357T>A NP_001369730.1:p.Phe1119Leu
NM_001382802.1:c.3303T>A NP_001369731.1:p.Phe1101Leu
NM_001382803.1:c.*140T>A NP_001369732.1:n.*140T>A
NM_001382804.1:c.2733T>A NP_001369733.1:p.Phe911Leu
NM_001382805.1:c.2610T>A NP_001369734.1:p.Phe870Leu
NM_001382806.1:c.2523T>A NP_001369735.1:p.Phe841Leu
NM_004448.4:c.3561T>A MANE Select NP_004439.2:p.Phe1187Leu
NR_110535.2:n.3799T>A