Canonical Allele Identifier: CA2637629136
Gene: ERBB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727548del , CM000679.2:g.39727548del GRCh38
NC_000017.10:g.37883801del , CM000679.1:g.37883801del GRCh37
NC_000017.9:g.35137327del NCBI36
NG_007503.1:g.44409del , LRG_724:g.44409del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.3412+1del
ENST00000269571.9:c.3412+1del
ENST00000406381.6:c.3322+1del
ENST00000445658.6:c.2584+1del
ENST00000541774.5:c.3367+1del
ENST00000578373.5:c.*3202+1del
ENST00000584450.5:c.3160-141del ENSP00000463714.1:n.3160-141del
ENST00000584601.5:c.3322+1del
NM_001005862.2:c.3322+1del , LRG_724t1:c.3322+1del
NM_001289936.1:c.3367+1del , LRG_724t4:c.3367+1del
NM_001289937.1:c.3160-141del NP_001276866.1:n.3160-141del
NM_004448.3:c.3412+1del , LRG_724t2:c.3412+1del
NR_110535.1:n.3736+1del
XM_024450641.1:c.3550+1del
XM_024450642.1:c.3505+1del
XM_024450643.1:c.3460+1del
NM_001005862.3:c.3322+1del
NM_001289936.2:c.3367+1del
NM_001289937.2:c.3160-141del NP_001276866.1:n.3160-141del
NM_001382782.1:c.3322+1del
NM_001382783.1:c.3322+1del
NM_001382784.1:c.3529+1del
NM_001382785.1:c.3514+1del
NM_001382786.1:c.3493+1del
NM_001382787.1:c.3487+1del
NM_001382788.1:c.3442+1del
NM_001382789.1:c.3433+1del
NM_001382790.1:c.3409+1del
NM_001382791.1:c.3403+1del
NM_001382792.1:c.3376+1del
NM_001382793.1:c.3370+1del
NM_001382794.1:c.3370+1del
NM_001382795.1:c.3364+1del
NM_001382796.1:c.3325+1del
NM_001382797.1:c.3313+1del
NM_001382798.1:c.3256+1del
NM_001382799.1:c.3232+1del
NM_001382800.1:c.3226+1del
NM_001382801.1:c.3208+1del
NM_001382802.1:c.3154+1del
NM_001382803.1:c.3118-141del NP_001369732.1:n.3118-141del
NM_001382804.1:c.2584+1del
NM_001382805.1:c.2461+1del
NM_001382806.1:c.2374+1del
NM_004448.4:c.3412+1del
NR_110535.2:n.3650+1del