Canonical Allele Identifier: CA2733615442

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145850684

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724819_39724820del , CM000679.2:g.39724819_39724820del	GRCh38
NC_000017.10:g.37881072_37881073del , CM000679.1:g.37881072_37881073del	GRCh37
NC_000017.9:g.35134598_35134599del	NCBI36
NG_007503.1:g.41680_41681del , LRG_724:g.41680_41681del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2401_2402del MANE Select	ENSP00000269571.4:p.Met801AlafsTer?
ENST00000269571.9:c.2401_2402del	ENSP00000269571.4:p.Met801AlafsTer?
ENST00000406381.6:c.2311_2312del	ENSP00000385185.2:p.Met771AlafsTer?
ENST00000445658.6:c.1573_1574del	ENSP00000404047.2:p.Met525AlafsTer?
ENST00000541774.5:c.2356_2357del	ENSP00000446466.1:p.Met786AlafsTer?
ENST00000578373.5:c.*2191_*2192del	ENSP00000463427.1:n.*2191_*2192del
ENST00000580074.1:c.507_508del
ENST00000583038.5:n.3535_3536del
ENST00000584450.5:c.2401_2402del	ENSP00000463714.1:p.Met801AlafsTer?
ENST00000584601.5:c.2311_2312del	ENSP00000462438.1:p.Met771AlafsTer?
NM_001005862.2:c.2311_2312del , LRG_724t1:c.2311_2312del	NP_001005862.1:p.Met771AlafsTer?
NM_001289936.1:c.2356_2357del , LRG_724t4:c.2356_2357del	NP_001276865.1:p.Met786AlafsTer?
NM_001289937.1:c.2401_2402del	NP_001276866.1:p.Met801AlafsTer?
NM_004448.3:c.2401_2402del , LRG_724t2:c.2401_2402del	NP_004439.2:p.Met801AlafsTer?
NR_110535.1:n.2725_2726del
XM_024450641.1:c.2539_2540del	XP_024306409.1:p.Met847AlafsTer?
XM_024450642.1:c.2494_2495del	XP_024306410.1:p.Met832AlafsTer?
XM_024450643.1:c.2449_2450del	XP_024306411.1:p.Met817AlafsTer?
NM_001005862.3:c.2311_2312del	NP_001005862.1:p.Met771AlafsTer?
NM_001289936.2:c.2356_2357del	NP_001276865.1:p.Met786AlafsTer?
NM_001289937.2:c.2401_2402del	NP_001276866.1:p.Met801AlafsTer?
NM_001382782.1:c.2311_2312del	NP_001369711.1:p.Met771AlafsTer?
NM_001382783.1:c.2311_2312del	NP_001369712.1:p.Met771AlafsTer?
NM_001382784.1:c.2518_2519del	NP_001369713.1:p.Met840AlafsTer?
NM_001382785.1:c.2503_2504del	NP_001369714.1:p.Met835AlafsTer?
NM_001382786.1:c.2482_2483del	NP_001369715.1:p.Met828AlafsTer?
NM_001382787.1:c.2476_2477del	NP_001369716.1:p.Met826AlafsTer?
NM_001382788.1:c.2431_2432del	NP_001369717.1:p.Met811AlafsTer?
NM_001382789.1:c.2422_2423del	NP_001369718.1:p.Met808AlafsTer?
NM_001382790.1:c.2398_2399del	NP_001369719.1:p.Met800AlafsTer?
NM_001382791.1:c.2392_2393del	NP_001369720.1:p.Met798AlafsTer?
NM_001382792.1:c.2365_2366del	NP_001369721.1:p.Met789AlafsTer?
NM_001382793.1:c.2359_2360del	NP_001369722.1:p.Met787AlafsTer?
NM_001382794.1:c.2359_2360del	NP_001369723.1:p.Met787AlafsTer?
NM_001382795.1:c.2353_2354del	NP_001369724.1:p.Met785AlafsTer?
NM_001382796.1:c.2401_2402del	NP_001369725.1:p.Met801AlafsTer?
NM_001382797.1:c.2302_2303del	NP_001369726.1:p.Met768AlafsTer?
NM_001382798.1:c.2401_2402del	NP_001369727.1:p.Met801AlafsTer?
NM_001382799.1:c.2221_2222del	NP_001369728.1:p.Met741AlafsTer?
NM_001382800.1:c.2308-230_2308-229del	NP_001369729.1:n.2308-230_2308-229del
NM_001382801.1:c.2353_2354del	NP_001369730.1:p.Met785AlafsTer?
NM_001382802.1:c.2143_2144del	NP_001369731.1:p.Met715AlafsTer?
NM_001382803.1:c.2359_2360del	NP_001369732.1:p.Met787AlafsTer?
NM_001382804.1:c.1573_1574del	NP_001369733.1:p.Met525AlafsTer?
NM_001382805.1:c.2208+1159_2208+1160del	NP_001369734.1:n.2208+1159_2208+1160del
NM_001382806.1:c.1363_1364del	NP_001369735.1:p.Met455AlafsTer?
NM_004448.4:c.2401_2402del MANE Select	NP_004439.2:p.Met801AlafsTer?
NR_110535.2:n.2639_2640del