Canonical Allele Identifier: CA2637621310

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39724607-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724609del , CM000679.2:g.39724609del	GRCh38
NC_000017.10:g.37880862del , CM000679.1:g.37880862del	GRCh37
NC_000017.9:g.35134388del	NCBI36
NG_007503.1:g.41470del , LRG_724:g.41470del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2308-117del MANE Select	ENSP00000269571.4:n.2308-117del
ENST00000269571.9:c.2308-117del	ENSP00000269571.4:n.2308-117del
ENST00000406381.6:c.2218-117del	ENSP00000385185.2:n.2218-117del
ENST00000445658.6:c.1480-117del	ENSP00000404047.2:n.1480-117del
ENST00000541774.5:c.2263-117del	ENSP00000446466.1:n.2263-117del
ENST00000578373.5:c.*2098-117del	ENSP00000463427.1:n.*2098-117del
ENST00000580074.1:c.414-117del
ENST00000583038.5:n.3442-117del
ENST00000584450.5:c.2308-117del	ENSP00000463714.1:n.2308-117del
ENST00000584601.5:c.2218-117del	ENSP00000462438.1:n.2218-117del
NM_001005862.2:c.2218-117del , LRG_724t1:c.2218-117del	NP_001005862.1:n.2218-117del
NM_001289936.1:c.2263-117del , LRG_724t4:c.2263-117del	NP_001276865.1:n.2263-117del
NM_001289937.1:c.2308-117del	NP_001276866.1:n.2308-117del
NM_004448.3:c.2308-117del , LRG_724t2:c.2308-117del	NP_004439.2:n.2308-117del
NR_110535.1:n.2632-117del
XM_024450641.1:c.2446-117del	XP_024306409.1:n.2446-117del
XM_024450642.1:c.2401-117del	XP_024306410.1:n.2401-117del
XM_024450643.1:c.2356-117del	XP_024306411.1:n.2356-117del
NM_001005862.3:c.2218-117del	NP_001005862.1:n.2218-117del
NM_001289936.2:c.2263-117del	NP_001276865.1:n.2263-117del
NM_001289937.2:c.2308-117del	NP_001276866.1:n.2308-117del
NM_001382782.1:c.2218-117del	NP_001369711.1:n.2218-117del
NM_001382783.1:c.2218-117del	NP_001369712.1:n.2218-117del
NM_001382784.1:c.2425-117del	NP_001369713.1:n.2425-117del
NM_001382785.1:c.2410-117del	NP_001369714.1:n.2410-117del
NM_001382786.1:c.2389-117del	NP_001369715.1:n.2389-117del
NM_001382787.1:c.2383-117del	NP_001369716.1:n.2383-117del
NM_001382788.1:c.2338-117del	NP_001369717.1:n.2338-117del
NM_001382789.1:c.2329-117del	NP_001369718.1:n.2329-117del
NM_001382790.1:c.2305-117del	NP_001369719.1:n.2305-117del
NM_001382791.1:c.2299-117del	NP_001369720.1:n.2299-117del
NM_001382792.1:c.2272-117del	NP_001369721.1:n.2272-117del
NM_001382793.1:c.2266-117del	NP_001369722.1:n.2266-117del
NM_001382794.1:c.2266-117del	NP_001369723.1:n.2266-117del
NM_001382795.1:c.2260-117del	NP_001369724.1:n.2260-117del
NM_001382796.1:c.2308-117del	NP_001369725.1:n.2308-117del
NM_001382797.1:c.2209-117del	NP_001369726.1:n.2209-117del
NM_001382798.1:c.2308-117del	NP_001369727.1:n.2308-117del
NM_001382799.1:c.2128-117del	NP_001369728.1:n.2128-117del
NM_001382800.1:c.2308-440del	NP_001369729.1:n.2308-440del
NM_001382801.1:c.2260-117del	NP_001369730.1:n.2260-117del
NM_001382802.1:c.2050-117del	NP_001369731.1:n.2050-117del
NM_001382803.1:c.2266-117del	NP_001369732.1:n.2266-117del
NM_001382804.1:c.1480-117del	NP_001369733.1:n.1480-117del
NM_001382805.1:c.2208+949del	NP_001369734.1:n.2208+949del
NM_001382806.1:c.1270-117del	NP_001369735.1:n.1270-117del
NM_004448.4:c.2308-117del MANE Select	NP_004439.2:n.2308-117del
NR_110535.2:n.2546-117del