Canonical Allele Identifier: CA2259229177
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727596A= , CM000679.2:g.39727596A= GRCh38
NC_000017.10:g.37883849A= , CM000679.1:g.37883849A= GRCh37
NC_000017.9:g.35137375A= NCBI36
NG_007503.1:g.44457A= , LRG_724:g.44457A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3412+49A= MANE Select ENSP00000269571.4:n.3412+49A=
ENST00000269571.9:c.3412+49A= ENSP00000269571.4:n.3412+49A=
ENST00000406381.6:c.3322+49A= ENSP00000385185.2:n.3322+49A=
ENST00000445658.6:c.2584+49A= ENSP00000404047.2:n.2584+49A=
ENST00000541774.5:c.3367+49A= ENSP00000446466.1:n.3367+49A=
ENST00000578373.5:c.*3202+49A= ENSP00000463427.1:n.*3202+49A=
ENST00000584450.5:c.3160-93A= ENSP00000463714.1:n.3160-93A=
ENST00000584601.5:c.3322+49A= ENSP00000462438.1:n.3322+49A=
NM_001005862.2:c.3322+49A= , LRG_724t1:c.3322+49A= NP_001005862.1:n.3322+49A=
NM_001289936.1:c.3367+49A= , LRG_724t4:c.3367+49A= NP_001276865.1:n.3367+49A=
NM_001289937.1:c.3160-93A= NP_001276866.1:n.3160-93A=
NM_004448.3:c.3412+49A= , LRG_724t2:c.3412+49A= NP_004439.2:n.3412+49A=
NR_110535.1:n.3736+49A=
XM_024450641.1:c.3550+49A= XP_024306409.1:n.3550+49A=
XM_024450642.1:c.3505+49A= XP_024306410.1:n.3505+49A=
XM_024450643.1:c.3460+49A= XP_024306411.1:n.3460+49A=
NM_001005862.3:c.3322+49A= NP_001005862.1:n.3322+49A=
NM_001289936.2:c.3367+49A= NP_001276865.1:n.3367+49A=
NM_001289937.2:c.3160-93A= NP_001276866.1:n.3160-93A=
NM_001382782.1:c.3322+49A= NP_001369711.1:n.3322+49A=
NM_001382783.1:c.3322+49A= NP_001369712.1:n.3322+49A=
NM_001382784.1:c.3529+49A= NP_001369713.1:n.3529+49A=
NM_001382785.1:c.3514+49A= NP_001369714.1:n.3514+49A=
NM_001382786.1:c.3493+49A= NP_001369715.1:n.3493+49A=
NM_001382787.1:c.3487+49A= NP_001369716.1:n.3487+49A=
NM_001382788.1:c.3442+49A= NP_001369717.1:n.3442+49A=
NM_001382789.1:c.3433+49A= NP_001369718.1:n.3433+49A=
NM_001382790.1:c.3409+49A= NP_001369719.1:n.3409+49A=
NM_001382791.1:c.3403+49A= NP_001369720.1:n.3403+49A=
NM_001382792.1:c.3376+49A= NP_001369721.1:n.3376+49A=
NM_001382793.1:c.3370+49A= NP_001369722.1:n.3370+49A=
NM_001382794.1:c.3370+49A= NP_001369723.1:n.3370+49A=
NM_001382795.1:c.3364+49A= NP_001369724.1:n.3364+49A=
NM_001382796.1:c.3325+49A= NP_001369725.1:n.3325+49A=
NM_001382797.1:c.3313+49A= NP_001369726.1:n.3313+49A=
NM_001382798.1:c.3256+49A= NP_001369727.1:n.3256+49A=
NM_001382799.1:c.3232+49A= NP_001369728.1:n.3232+49A=
NM_001382800.1:c.3226+49A= NP_001369729.1:n.3226+49A=
NM_001382801.1:c.3208+49A= NP_001369730.1:n.3208+49A=
NM_001382802.1:c.3154+49A= NP_001369731.1:n.3154+49A=
NM_001382803.1:c.3118-93A= NP_001369732.1:n.3118-93A=
NM_001382804.1:c.2584+49A= NP_001369733.1:n.2584+49A=
NM_001382805.1:c.2461+49A= NP_001369734.1:n.2461+49A=
NM_001382806.1:c.2374+49A= NP_001369735.1:n.2374+49A=
NM_004448.4:c.3412+49A= MANE Select NP_004439.2:n.3412+49A=
NR_110535.2:n.3650+49A=