Canonical Allele Identifier: CA771855496

Gene: ERBB2

Linked Data

• dbSNP Id: rs1366079375
• gnomAD v4: 17-39724670-GTGGTGT-G
• MyVariant Identifiers: chr17:g.37880924_37880929del (hg19) ; chr17:g.39724671_39724676del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724672_39724677del , CM000679.2:g.39724672_39724677del	GRCh38
NC_000017.10:g.37880925_37880930del , CM000679.1:g.37880925_37880930del	GRCh37
NC_000017.9:g.35134451_35134456del	NCBI36
NG_007503.1:g.41533_41538del , LRG_724:g.41533_41538del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2308-54_2308-49del MANE Select	ENSP00000269571.4:n.2308-54_2308-49del
ENST00000269571.9:c.2308-54_2308-49del	ENSP00000269571.4:n.2308-54_2308-49del
ENST00000406381.6:c.2218-54_2218-49del	ENSP00000385185.2:n.2218-54_2218-49del
ENST00000445658.6:c.1480-54_1480-49del	ENSP00000404047.2:n.1480-54_1480-49del
ENST00000541774.5:c.2263-54_2263-49del	ENSP00000446466.1:n.2263-54_2263-49del
ENST00000578373.5:c.*2098-54_*2098-49del	ENSP00000463427.1:n.*2098-54_*2098-49del
ENST00000580074.1:c.414-54_414-49del
ENST00000583038.5:n.3442-54_3442-49del
ENST00000584450.5:c.2308-54_2308-49del	ENSP00000463714.1:n.2308-54_2308-49del
ENST00000584601.5:c.2218-54_2218-49del	ENSP00000462438.1:n.2218-54_2218-49del
NM_001005862.2:c.2218-54_2218-49del , LRG_724t1:c.2218-54_2218-49del	NP_001005862.1:n.2218-54_2218-49del
NM_001289936.1:c.2263-54_2263-49del , LRG_724t4:c.2263-54_2263-49del	NP_001276865.1:n.2263-54_2263-49del
NM_001289937.1:c.2308-54_2308-49del	NP_001276866.1:n.2308-54_2308-49del
NM_004448.3:c.2308-54_2308-49del , LRG_724t2:c.2308-54_2308-49del	NP_004439.2:n.2308-54_2308-49del
NR_110535.1:n.2632-54_2632-49del
XM_024450641.1:c.2446-54_2446-49del	XP_024306409.1:n.2446-54_2446-49del
XM_024450642.1:c.2401-54_2401-49del	XP_024306410.1:n.2401-54_2401-49del
XM_024450643.1:c.2356-54_2356-49del	XP_024306411.1:n.2356-54_2356-49del
NM_001005862.3:c.2218-54_2218-49del	NP_001005862.1:n.2218-54_2218-49del
NM_001289936.2:c.2263-54_2263-49del	NP_001276865.1:n.2263-54_2263-49del
NM_001289937.2:c.2308-54_2308-49del	NP_001276866.1:n.2308-54_2308-49del
NM_001382782.1:c.2218-54_2218-49del	NP_001369711.1:n.2218-54_2218-49del
NM_001382783.1:c.2218-54_2218-49del	NP_001369712.1:n.2218-54_2218-49del
NM_001382784.1:c.2425-54_2425-49del	NP_001369713.1:n.2425-54_2425-49del
NM_001382785.1:c.2410-54_2410-49del	NP_001369714.1:n.2410-54_2410-49del
NM_001382786.1:c.2389-54_2389-49del	NP_001369715.1:n.2389-54_2389-49del
NM_001382787.1:c.2383-54_2383-49del	NP_001369716.1:n.2383-54_2383-49del
NM_001382788.1:c.2338-54_2338-49del	NP_001369717.1:n.2338-54_2338-49del
NM_001382789.1:c.2329-54_2329-49del	NP_001369718.1:n.2329-54_2329-49del
NM_001382790.1:c.2305-54_2305-49del	NP_001369719.1:n.2305-54_2305-49del
NM_001382791.1:c.2299-54_2299-49del	NP_001369720.1:n.2299-54_2299-49del
NM_001382792.1:c.2272-54_2272-49del	NP_001369721.1:n.2272-54_2272-49del
NM_001382793.1:c.2266-54_2266-49del	NP_001369722.1:n.2266-54_2266-49del
NM_001382794.1:c.2266-54_2266-49del	NP_001369723.1:n.2266-54_2266-49del
NM_001382795.1:c.2260-54_2260-49del	NP_001369724.1:n.2260-54_2260-49del
NM_001382796.1:c.2308-54_2308-49del	NP_001369725.1:n.2308-54_2308-49del
NM_001382797.1:c.2209-54_2209-49del	NP_001369726.1:n.2209-54_2209-49del
NM_001382798.1:c.2308-54_2308-49del	NP_001369727.1:n.2308-54_2308-49del
NM_001382799.1:c.2128-54_2128-49del	NP_001369728.1:n.2128-54_2128-49del
NM_001382800.1:c.2308-377_2308-372del	NP_001369729.1:n.2308-377_2308-372del
NM_001382801.1:c.2260-54_2260-49del	NP_001369730.1:n.2260-54_2260-49del
NM_001382802.1:c.2050-54_2050-49del	NP_001369731.1:n.2050-54_2050-49del
NM_001382803.1:c.2266-54_2266-49del	NP_001369732.1:n.2266-54_2266-49del
NM_001382804.1:c.1480-54_1480-49del	NP_001369733.1:n.1480-54_1480-49del
NM_001382805.1:c.2208+1012_2208+1017del	NP_001369734.1:n.2208+1012_2208+1017del
NM_001382806.1:c.1270-54_1270-49del	NP_001369735.1:n.1270-54_1270-49del
NM_004448.4:c.2308-54_2308-49del MANE Select	NP_004439.2:n.2308-54_2308-49del
NR_110535.2:n.2546-54_2546-49del