Canonical Allele Identifier: CA399312790
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727541C>A , CM000679.2:g.39727541C>A GRCh38
NC_000017.10:g.37883794C>A , CM000679.1:g.37883794C>A GRCh37
NC_000017.9:g.35137320C>A NCBI36
NG_007503.1:g.44402C>A , LRG_724:g.44402C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3406C>A MANE Select ENSP00000269571.4:p.Gln1136Lys
ENST00000269571.9:c.3406C>A ENSP00000269571.4:p.Gln1136Lys
ENST00000406381.6:c.3316C>A ENSP00000385185.2:p.Gln1106Lys
ENST00000445658.6:c.2578C>A ENSP00000404047.2:p.Gln860Lys
ENST00000541774.5:c.3361C>A ENSP00000446466.1:p.Gln1121Lys
ENST00000578373.5:c.*3196C>A ENSP00000463427.1:n.*3196C>A
ENST00000584450.5:c.3160-148C>A ENSP00000463714.1:n.3160-148C>A
ENST00000584601.5:c.3316C>A ENSP00000462438.1:p.Gln1106Lys
NM_001005862.2:c.3316C>A , LRG_724t1:c.3316C>A NP_001005862.1:p.Gln1106Lys
NM_001289936.1:c.3361C>A , LRG_724t4:c.3361C>A NP_001276865.1:p.Gln1121Lys
NM_001289937.1:c.3160-148C>A NP_001276866.1:n.3160-148C>A
NM_004448.3:c.3406C>A , LRG_724t2:c.3406C>A NP_004439.2:p.Gln1136Lys
NR_110535.1:n.3730C>A
XM_024450641.1:c.3544C>A XP_024306409.1:p.Gln1182Lys
XM_024450642.1:c.3499C>A XP_024306410.1:p.Gln1167Lys
XM_024450643.1:c.3454C>A XP_024306411.1:p.Gln1152Lys
NM_001005862.3:c.3316C>A NP_001005862.1:p.Gln1106Lys
NM_001289936.2:c.3361C>A NP_001276865.1:p.Gln1121Lys
NM_001289937.2:c.3160-148C>A NP_001276866.1:n.3160-148C>A
NM_001382782.1:c.3316C>A NP_001369711.1:p.Gln1106Lys
NM_001382783.1:c.3316C>A NP_001369712.1:p.Gln1106Lys
NM_001382784.1:c.3523C>A NP_001369713.1:p.Gln1175Lys
NM_001382785.1:c.3508C>A NP_001369714.1:p.Gln1170Lys
NM_001382786.1:c.3487C>A NP_001369715.1:p.Gln1163Lys
NM_001382787.1:c.3481C>A NP_001369716.1:p.Gln1161Lys
NM_001382788.1:c.3436C>A NP_001369717.1:p.Gln1146Lys
NM_001382789.1:c.3427C>A NP_001369718.1:p.Gln1143Lys
NM_001382790.1:c.3403C>A NP_001369719.1:p.Gln1135Lys
NM_001382791.1:c.3397C>A NP_001369720.1:p.Gln1133Lys
NM_001382792.1:c.3370C>A NP_001369721.1:p.Gln1124Lys
NM_001382793.1:c.3364C>A NP_001369722.1:p.Gln1122Lys
NM_001382794.1:c.3364C>A NP_001369723.1:p.Gln1122Lys
NM_001382795.1:c.3358C>A NP_001369724.1:p.Gln1120Lys
NM_001382796.1:c.3319C>A NP_001369725.1:p.Gln1107Lys
NM_001382797.1:c.3307C>A NP_001369726.1:p.Gln1103Lys
NM_001382798.1:c.3250C>A NP_001369727.1:p.Gln1084Lys
NM_001382799.1:c.3226C>A NP_001369728.1:p.Gln1076Lys
NM_001382800.1:c.3220C>A NP_001369729.1:p.Gln1074Lys
NM_001382801.1:c.3202C>A NP_001369730.1:p.Gln1068Lys
NM_001382802.1:c.3148C>A NP_001369731.1:p.Gln1050Lys
NM_001382803.1:c.3118-148C>A NP_001369732.1:n.3118-148C>A
NM_001382804.1:c.2578C>A NP_001369733.1:p.Gln860Lys
NM_001382805.1:c.2455C>A NP_001369734.1:p.Gln819Lys
NM_001382806.1:c.2368C>A NP_001369735.1:p.Gln790Lys
NM_004448.4:c.3406C>A MANE Select NP_004439.2:p.Gln1136Lys
NR_110535.2:n.3644C>A