Canonical Allele Identifier: CA771855364

Gene: ERBB2

Linked Data

• dbSNP Id: rs71149796
• gnomAD v3: 17-39724272-A-ATTTTTTT
• gnomAD v4: 17-39724272-A-ATTTTTTT
• MyVariant Identifiers: chr17:g.37880525_37880526insTTTTTTT (hg19) ; chr17:g.39724272_39724273insTTTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724282_39724288dup , CM000679.2:g.39724282_39724288dup	GRCh38
NC_000017.10:g.37880535_37880541dup , CM000679.1:g.37880535_37880541dup	GRCh37
NC_000017.9:g.35134061_35134067dup	NCBI36
NG_007503.1:g.41143_41149dup , LRG_724:g.41143_41149dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2307+272_2307+278dup MANE Select	ENSP00000269571.4:n.2307+272_2307+278dup
ENST00000269571.9:c.2307+272_2307+278dup	ENSP00000269571.4:n.2307+272_2307+278dup
ENST00000406381.6:c.2217+272_2217+278dup	ENSP00000385185.2:n.2217+272_2217+278dup
ENST00000445658.6:c.1479+272_1479+278dup	ENSP00000404047.2:n.1479+272_1479+278dup
ENST00000541774.5:c.2262+272_2262+278dup	ENSP00000446466.1:n.2262+272_2262+278dup
ENST00000578373.5:c.*2097+272_*2097+278dup	ENSP00000463427.1:n.*2097+272_*2097+278dup
ENST00000580074.1:c.413+272_413+278dup
ENST00000583038.5:n.3441+272_3441+278dup
ENST00000584450.5:c.2307+272_2307+278dup	ENSP00000463714.1:n.2307+272_2307+278dup
ENST00000584601.5:c.2217+272_2217+278dup	ENSP00000462438.1:n.2217+272_2217+278dup
NM_001005862.2:c.2217+272_2217+278dup , LRG_724t1:c.2217+272_2217+278dup	NP_001005862.1:n.2217+272_2217+278dup
NM_001289936.1:c.2262+272_2262+278dup , LRG_724t4:c.2262+272_2262+278dup	NP_001276865.1:n.2262+272_2262+278dup
NM_001289937.1:c.2307+272_2307+278dup	NP_001276866.1:n.2307+272_2307+278dup
NM_004448.3:c.2307+272_2307+278dup , LRG_724t2:c.2307+272_2307+278dup	NP_004439.2:n.2307+272_2307+278dup
NR_110535.1:n.2631+272_2631+278dup
XM_024450641.1:c.2445+272_2445+278dup	XP_024306409.1:n.2445+272_2445+278dup
XM_024450642.1:c.2400+272_2400+278dup	XP_024306410.1:n.2400+272_2400+278dup
XM_024450643.1:c.2355+272_2355+278dup	XP_024306411.1:n.2355+272_2355+278dup
NM_001005862.3:c.2217+272_2217+278dup	NP_001005862.1:n.2217+272_2217+278dup
NM_001289936.2:c.2262+272_2262+278dup	NP_001276865.1:n.2262+272_2262+278dup
NM_001289937.2:c.2307+272_2307+278dup	NP_001276866.1:n.2307+272_2307+278dup
NM_001382782.1:c.2217+272_2217+278dup	NP_001369711.1:n.2217+272_2217+278dup
NM_001382783.1:c.2217+272_2217+278dup	NP_001369712.1:n.2217+272_2217+278dup
NM_001382784.1:c.2424+272_2424+278dup	NP_001369713.1:n.2424+272_2424+278dup
NM_001382785.1:c.2409+272_2409+278dup	NP_001369714.1:n.2409+272_2409+278dup
NM_001382786.1:c.2388+272_2388+278dup	NP_001369715.1:n.2388+272_2388+278dup
NM_001382787.1:c.2382+272_2382+278dup	NP_001369716.1:n.2382+272_2382+278dup
NM_001382788.1:c.2337+272_2337+278dup	NP_001369717.1:n.2337+272_2337+278dup
NM_001382789.1:c.2328+272_2328+278dup	NP_001369718.1:n.2328+272_2328+278dup
NM_001382790.1:c.2304+272_2304+278dup	NP_001369719.1:n.2304+272_2304+278dup
NM_001382791.1:c.2298+272_2298+278dup	NP_001369720.1:n.2298+272_2298+278dup
NM_001382792.1:c.2271+272_2271+278dup	NP_001369721.1:n.2271+272_2271+278dup
NM_001382793.1:c.2265+272_2265+278dup	NP_001369722.1:n.2265+272_2265+278dup
NM_001382794.1:c.2265+272_2265+278dup	NP_001369723.1:n.2265+272_2265+278dup
NM_001382795.1:c.2259+272_2259+278dup	NP_001369724.1:n.2259+272_2259+278dup
NM_001382796.1:c.2307+272_2307+278dup	NP_001369725.1:n.2307+272_2307+278dup
NM_001382797.1:c.2209-444_2209-438dup	NP_001369726.1:n.2209-444_2209-438dup
NM_001382798.1:c.2307+272_2307+278dup	NP_001369727.1:n.2307+272_2307+278dup
NM_001382799.1:c.2127+272_2127+278dup	NP_001369728.1:n.2127+272_2127+278dup
NM_001382800.1:c.2307+272_2307+278dup	NP_001369729.1:n.2307+272_2307+278dup
NM_001382801.1:c.2259+272_2259+278dup	NP_001369730.1:n.2259+272_2259+278dup
NM_001382802.1:c.2049+272_2049+278dup	NP_001369731.1:n.2049+272_2049+278dup
NM_001382803.1:c.2265+272_2265+278dup	NP_001369732.1:n.2265+272_2265+278dup
NM_001382804.1:c.1479+272_1479+278dup	NP_001369733.1:n.1479+272_1479+278dup
NM_001382805.1:c.2208+622_2208+628dup	NP_001369734.1:n.2208+622_2208+628dup
NM_001382806.1:c.1269+272_1269+278dup	NP_001369735.1:n.1269+272_1269+278dup
NM_004448.4:c.2307+272_2307+278dup MANE Select	NP_004439.2:n.2307+272_2307+278dup
NR_110535.2:n.2545+272_2545+278dup