Canonical Allele Identifier: CA2637621387

Gene: ERBB2

Linked Data

• gnomAD v4: 17-39724638-ATGGCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724642_39724647del , CM000679.2:g.39724642_39724647del	GRCh38
NC_000017.10:g.37880895_37880900del , CM000679.1:g.37880895_37880900del	GRCh37
NC_000017.9:g.35134421_35134426del	NCBI36
NG_007503.1:g.41503_41508del , LRG_724:g.41503_41508del

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2308-84_2308-79del MANE Select	ENSP00000269571.4:n.2308-84_2308-79del
ENST00000269571.9:c.2308-84_2308-79del	ENSP00000269571.4:n.2308-84_2308-79del
ENST00000406381.6:c.2218-84_2218-79del	ENSP00000385185.2:n.2218-84_2218-79del
ENST00000445658.6:c.1480-84_1480-79del	ENSP00000404047.2:n.1480-84_1480-79del
ENST00000541774.5:c.2263-84_2263-79del	ENSP00000446466.1:n.2263-84_2263-79del
ENST00000578373.5:c.*2098-84_*2098-79del	ENSP00000463427.1:n.*2098-84_*2098-79del
ENST00000580074.1:c.414-84_414-79del
ENST00000583038.5:n.3442-84_3442-79del
ENST00000584450.5:c.2308-84_2308-79del	ENSP00000463714.1:n.2308-84_2308-79del
ENST00000584601.5:c.2218-84_2218-79del	ENSP00000462438.1:n.2218-84_2218-79del
NM_001005862.2:c.2218-84_2218-79del , LRG_724t1:c.2218-84_2218-79del	NP_001005862.1:n.2218-84_2218-79del
NM_001289936.1:c.2263-84_2263-79del , LRG_724t4:c.2263-84_2263-79del	NP_001276865.1:n.2263-84_2263-79del
NM_001289937.1:c.2308-84_2308-79del	NP_001276866.1:n.2308-84_2308-79del
NM_004448.3:c.2308-84_2308-79del , LRG_724t2:c.2308-84_2308-79del	NP_004439.2:n.2308-84_2308-79del
NR_110535.1:n.2632-84_2632-79del
XM_024450641.1:c.2446-84_2446-79del	XP_024306409.1:n.2446-84_2446-79del
XM_024450642.1:c.2401-84_2401-79del	XP_024306410.1:n.2401-84_2401-79del
XM_024450643.1:c.2356-84_2356-79del	XP_024306411.1:n.2356-84_2356-79del
NM_001005862.3:c.2218-84_2218-79del	NP_001005862.1:n.2218-84_2218-79del
NM_001289936.2:c.2263-84_2263-79del	NP_001276865.1:n.2263-84_2263-79del
NM_001289937.2:c.2308-84_2308-79del	NP_001276866.1:n.2308-84_2308-79del
NM_001382782.1:c.2218-84_2218-79del	NP_001369711.1:n.2218-84_2218-79del
NM_001382783.1:c.2218-84_2218-79del	NP_001369712.1:n.2218-84_2218-79del
NM_001382784.1:c.2425-84_2425-79del	NP_001369713.1:n.2425-84_2425-79del
NM_001382785.1:c.2410-84_2410-79del	NP_001369714.1:n.2410-84_2410-79del
NM_001382786.1:c.2389-84_2389-79del	NP_001369715.1:n.2389-84_2389-79del
NM_001382787.1:c.2383-84_2383-79del	NP_001369716.1:n.2383-84_2383-79del
NM_001382788.1:c.2338-84_2338-79del	NP_001369717.1:n.2338-84_2338-79del
NM_001382789.1:c.2329-84_2329-79del	NP_001369718.1:n.2329-84_2329-79del
NM_001382790.1:c.2305-84_2305-79del	NP_001369719.1:n.2305-84_2305-79del
NM_001382791.1:c.2299-84_2299-79del	NP_001369720.1:n.2299-84_2299-79del
NM_001382792.1:c.2272-84_2272-79del	NP_001369721.1:n.2272-84_2272-79del
NM_001382793.1:c.2266-84_2266-79del	NP_001369722.1:n.2266-84_2266-79del
NM_001382794.1:c.2266-84_2266-79del	NP_001369723.1:n.2266-84_2266-79del
NM_001382795.1:c.2260-84_2260-79del	NP_001369724.1:n.2260-84_2260-79del
NM_001382796.1:c.2308-84_2308-79del	NP_001369725.1:n.2308-84_2308-79del
NM_001382797.1:c.2209-84_2209-79del	NP_001369726.1:n.2209-84_2209-79del
NM_001382798.1:c.2308-84_2308-79del	NP_001369727.1:n.2308-84_2308-79del
NM_001382799.1:c.2128-84_2128-79del	NP_001369728.1:n.2128-84_2128-79del
NM_001382800.1:c.2308-407_2308-402del	NP_001369729.1:n.2308-407_2308-402del
NM_001382801.1:c.2260-84_2260-79del	NP_001369730.1:n.2260-84_2260-79del
NM_001382802.1:c.2050-84_2050-79del	NP_001369731.1:n.2050-84_2050-79del
NM_001382803.1:c.2266-84_2266-79del	NP_001369732.1:n.2266-84_2266-79del
NM_001382804.1:c.1480-84_1480-79del	NP_001369733.1:n.1480-84_1480-79del
NM_001382805.1:c.2208+982_2208+987del	NP_001369734.1:n.2208+982_2208+987del
NM_001382806.1:c.1270-84_1270-79del	NP_001369735.1:n.1270-84_1270-79del
NM_004448.4:c.2308-84_2308-79del MANE Select	NP_004439.2:n.2308-84_2308-79del
NR_110535.2:n.2546-84_2546-79del