Canonical Allele Identifier: CA499890261
Gene: ERBB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.37883742A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727489A>G , CM000679.2:g.39727489A>G GRCh38
NC_000017.10:g.37883742A>G , CM000679.1:g.37883742A>G GRCh37
NC_000017.9:g.35137268A>G NCBI36
NG_007503.1:g.44350A>G , LRG_724:g.44350A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3354A>G MANE Select ENSP00000269571.4:p.Val1118=
ENST00000269571.9:c.3354A>G ENSP00000269571.4:p.Val1118=
ENST00000406381.6:c.3264A>G ENSP00000385185.2:p.Val1088=
ENST00000445658.6:c.2526A>G ENSP00000404047.2:p.Val842=
ENST00000541774.5:c.3309A>G ENSP00000446466.1:p.Val1103=
ENST00000578373.5:c.*3144A>G ENSP00000463427.1:n.*3144A>G
ENST00000584450.5:c.3160-200A>G ENSP00000463714.1:n.3160-200A>G
ENST00000584601.5:c.3264A>G ENSP00000462438.1:p.Val1088=
NM_001005862.2:c.3264A>G , LRG_724t1:c.3264A>G NP_001005862.1:p.Val1088=
NM_001289936.1:c.3309A>G , LRG_724t4:c.3309A>G NP_001276865.1:p.Val1103=
NM_001289937.1:c.3160-200A>G NP_001276866.1:n.3160-200A>G
NM_004448.3:c.3354A>G , LRG_724t2:c.3354A>G NP_004439.2:p.Val1118=
NR_110535.1:n.3678A>G
XM_024450641.1:c.3492A>G XP_024306409.1:p.Val1164=
XM_024450642.1:c.3447A>G XP_024306410.1:p.Val1149=
XM_024450643.1:c.3402A>G XP_024306411.1:p.Val1134=
NM_001005862.3:c.3264A>G NP_001005862.1:p.Val1088=
NM_001289936.2:c.3309A>G NP_001276865.1:p.Val1103=
NM_001289937.2:c.3160-200A>G NP_001276866.1:n.3160-200A>G
NM_001382782.1:c.3264A>G NP_001369711.1:p.Val1088=
NM_001382783.1:c.3264A>G NP_001369712.1:p.Val1088=
NM_001382784.1:c.3471A>G NP_001369713.1:p.Val1157=
NM_001382785.1:c.3456A>G NP_001369714.1:p.Val1152=
NM_001382786.1:c.3435A>G NP_001369715.1:p.Val1145=
NM_001382787.1:c.3429A>G NP_001369716.1:p.Val1143=
NM_001382788.1:c.3384A>G NP_001369717.1:p.Val1128=
NM_001382789.1:c.3375A>G NP_001369718.1:p.Val1125=
NM_001382790.1:c.3351A>G NP_001369719.1:p.Val1117=
NM_001382791.1:c.3345A>G NP_001369720.1:p.Val1115=
NM_001382792.1:c.3318A>G NP_001369721.1:p.Val1106=
NM_001382793.1:c.3312A>G NP_001369722.1:p.Val1104=
NM_001382794.1:c.3312A>G NP_001369723.1:p.Val1104=
NM_001382795.1:c.3306A>G NP_001369724.1:p.Val1102=
NM_001382796.1:c.3267A>G NP_001369725.1:p.Val1089=
NM_001382797.1:c.3255A>G NP_001369726.1:p.Val1085=
NM_001382798.1:c.3198A>G NP_001369727.1:p.Val1066=
NM_001382799.1:c.3174A>G NP_001369728.1:p.Val1058=
NM_001382800.1:c.3168A>G NP_001369729.1:p.Val1056=
NM_001382801.1:c.3150A>G NP_001369730.1:p.Val1050=
NM_001382802.1:c.3096A>G NP_001369731.1:p.Val1032=
NM_001382803.1:c.3118-200A>G NP_001369732.1:n.3118-200A>G
NM_001382804.1:c.2526A>G NP_001369733.1:p.Val842=
NM_001382805.1:c.2403A>G NP_001369734.1:p.Val801=
NM_001382806.1:c.2316A>G NP_001369735.1:p.Val772=
NM_004448.4:c.3354A>G MANE Select NP_004439.2:p.Val1118=
NR_110535.2:n.3592A>G