Canonical Allele Identifier: CA2259229160
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727562C= , CM000679.2:g.39727562C= GRCh38
NC_000017.10:g.37883815C= , CM000679.1:g.37883815C= GRCh37
NC_000017.9:g.35137341C= NCBI36
NG_007503.1:g.44423C= , LRG_724:g.44423C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3412+15C= MANE Select ENSP00000269571.4:n.3412+15C=
ENST00000269571.9:c.3412+15C= ENSP00000269571.4:n.3412+15C=
ENST00000406381.6:c.3322+15C= ENSP00000385185.2:n.3322+15C=
ENST00000445658.6:c.2584+15C= ENSP00000404047.2:n.2584+15C=
ENST00000541774.5:c.3367+15C= ENSP00000446466.1:n.3367+15C=
ENST00000578373.5:c.*3202+15C= ENSP00000463427.1:n.*3202+15C=
ENST00000584450.5:c.3160-127C= ENSP00000463714.1:n.3160-127C=
ENST00000584601.5:c.3322+15C= ENSP00000462438.1:n.3322+15C=
NM_001005862.2:c.3322+15C= , LRG_724t1:c.3322+15C= NP_001005862.1:n.3322+15C=
NM_001289936.1:c.3367+15C= , LRG_724t4:c.3367+15C= NP_001276865.1:n.3367+15C=
NM_001289937.1:c.3160-127C= NP_001276866.1:n.3160-127C=
NM_004448.3:c.3412+15C= , LRG_724t2:c.3412+15C= NP_004439.2:n.3412+15C=
NR_110535.1:n.3736+15C=
XM_024450641.1:c.3550+15C= XP_024306409.1:n.3550+15C=
XM_024450642.1:c.3505+15C= XP_024306410.1:n.3505+15C=
XM_024450643.1:c.3460+15C= XP_024306411.1:n.3460+15C=
NM_001005862.3:c.3322+15C= NP_001005862.1:n.3322+15C=
NM_001289936.2:c.3367+15C= NP_001276865.1:n.3367+15C=
NM_001289937.2:c.3160-127C= NP_001276866.1:n.3160-127C=
NM_001382782.1:c.3322+15C= NP_001369711.1:n.3322+15C=
NM_001382783.1:c.3322+15C= NP_001369712.1:n.3322+15C=
NM_001382784.1:c.3529+15C= NP_001369713.1:n.3529+15C=
NM_001382785.1:c.3514+15C= NP_001369714.1:n.3514+15C=
NM_001382786.1:c.3493+15C= NP_001369715.1:n.3493+15C=
NM_001382787.1:c.3487+15C= NP_001369716.1:n.3487+15C=
NM_001382788.1:c.3442+15C= NP_001369717.1:n.3442+15C=
NM_001382789.1:c.3433+15C= NP_001369718.1:n.3433+15C=
NM_001382790.1:c.3409+15C= NP_001369719.1:n.3409+15C=
NM_001382791.1:c.3403+15C= NP_001369720.1:n.3403+15C=
NM_001382792.1:c.3376+15C= NP_001369721.1:n.3376+15C=
NM_001382793.1:c.3370+15C= NP_001369722.1:n.3370+15C=
NM_001382794.1:c.3370+15C= NP_001369723.1:n.3370+15C=
NM_001382795.1:c.3364+15C= NP_001369724.1:n.3364+15C=
NM_001382796.1:c.3325+15C= NP_001369725.1:n.3325+15C=
NM_001382797.1:c.3313+15C= NP_001369726.1:n.3313+15C=
NM_001382798.1:c.3256+15C= NP_001369727.1:n.3256+15C=
NM_001382799.1:c.3232+15C= NP_001369728.1:n.3232+15C=
NM_001382800.1:c.3226+15C= NP_001369729.1:n.3226+15C=
NM_001382801.1:c.3208+15C= NP_001369730.1:n.3208+15C=
NM_001382802.1:c.3154+15C= NP_001369731.1:n.3154+15C=
NM_001382803.1:c.3118-127C= NP_001369732.1:n.3118-127C=
NM_001382804.1:c.2584+15C= NP_001369733.1:n.2584+15C=
NM_001382805.1:c.2461+15C= NP_001369734.1:n.2461+15C=
NM_001382806.1:c.2374+15C= NP_001369735.1:n.2374+15C=
NM_004448.4:c.3412+15C= MANE Select NP_004439.2:n.3412+15C=
NR_110535.2:n.3650+15C=