Canonical Allele Identifier: CA625937577

Gene: ERBB2

Linked Data

• dbSNP Id: rs1277534624
• gnomAD v2: 17-37880555-G-GCTCTGTCA
• gnomAD v3: 17-39724302-G-GCTCTGTCA
• gnomAD v4: 17-39724302-G-GCTCTGTCA
• MyVariant Identifiers: chr17:g.37880555_37880556insCTCTGTCA (hg19) ; chr17:g.39724302_39724303insCTCTGTCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724304_39724311dup , CM000679.2:g.39724304_39724311dup	GRCh38
NC_000017.10:g.37880557_37880564dup , CM000679.1:g.37880557_37880564dup	GRCh37
NC_000017.9:g.35134083_35134090dup	NCBI36
NG_007503.1:g.41165_41172dup , LRG_724:g.41165_41172dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2307+294_2307+301dup MANE Select	ENSP00000269571.4:n.2307+294_2307+301dup
ENST00000269571.9:c.2307+294_2307+301dup	ENSP00000269571.4:n.2307+294_2307+301dup
ENST00000406381.6:c.2217+294_2217+301dup	ENSP00000385185.2:n.2217+294_2217+301dup
ENST00000445658.6:c.1479+294_1479+301dup	ENSP00000404047.2:n.1479+294_1479+301dup
ENST00000541774.5:c.2262+294_2262+301dup	ENSP00000446466.1:n.2262+294_2262+301dup
ENST00000578373.5:c.*2097+294_*2097+301dup	ENSP00000463427.1:n.*2097+294_*2097+301dup
ENST00000580074.1:c.413+294_413+301dup
ENST00000583038.5:n.3441+294_3441+301dup
ENST00000584450.5:c.2307+294_2307+301dup	ENSP00000463714.1:n.2307+294_2307+301dup
ENST00000584601.5:c.2217+294_2217+301dup	ENSP00000462438.1:n.2217+294_2217+301dup
NM_001005862.2:c.2217+294_2217+301dup , LRG_724t1:c.2217+294_2217+301dup	NP_001005862.1:n.2217+294_2217+301dup
NM_001289936.1:c.2262+294_2262+301dup , LRG_724t4:c.2262+294_2262+301dup	NP_001276865.1:n.2262+294_2262+301dup
NM_001289937.1:c.2307+294_2307+301dup	NP_001276866.1:n.2307+294_2307+301dup
NM_004448.3:c.2307+294_2307+301dup , LRG_724t2:c.2307+294_2307+301dup	NP_004439.2:n.2307+294_2307+301dup
NR_110535.1:n.2631+294_2631+301dup
XM_024450641.1:c.2445+294_2445+301dup	XP_024306409.1:n.2445+294_2445+301dup
XM_024450642.1:c.2400+294_2400+301dup	XP_024306410.1:n.2400+294_2400+301dup
XM_024450643.1:c.2355+294_2355+301dup	XP_024306411.1:n.2355+294_2355+301dup
NM_001005862.3:c.2217+294_2217+301dup	NP_001005862.1:n.2217+294_2217+301dup
NM_001289936.2:c.2262+294_2262+301dup	NP_001276865.1:n.2262+294_2262+301dup
NM_001289937.2:c.2307+294_2307+301dup	NP_001276866.1:n.2307+294_2307+301dup
NM_001382782.1:c.2217+294_2217+301dup	NP_001369711.1:n.2217+294_2217+301dup
NM_001382783.1:c.2217+294_2217+301dup	NP_001369712.1:n.2217+294_2217+301dup
NM_001382784.1:c.2424+294_2424+301dup	NP_001369713.1:n.2424+294_2424+301dup
NM_001382785.1:c.2409+294_2409+301dup	NP_001369714.1:n.2409+294_2409+301dup
NM_001382786.1:c.2388+294_2388+301dup	NP_001369715.1:n.2388+294_2388+301dup
NM_001382787.1:c.2382+294_2382+301dup	NP_001369716.1:n.2382+294_2382+301dup
NM_001382788.1:c.2337+294_2337+301dup	NP_001369717.1:n.2337+294_2337+301dup
NM_001382789.1:c.2328+294_2328+301dup	NP_001369718.1:n.2328+294_2328+301dup
NM_001382790.1:c.2304+294_2304+301dup	NP_001369719.1:n.2304+294_2304+301dup
NM_001382791.1:c.2298+294_2298+301dup	NP_001369720.1:n.2298+294_2298+301dup
NM_001382792.1:c.2271+294_2271+301dup	NP_001369721.1:n.2271+294_2271+301dup
NM_001382793.1:c.2265+294_2265+301dup	NP_001369722.1:n.2265+294_2265+301dup
NM_001382794.1:c.2265+294_2265+301dup	NP_001369723.1:n.2265+294_2265+301dup
NM_001382795.1:c.2259+294_2259+301dup	NP_001369724.1:n.2259+294_2259+301dup
NM_001382796.1:c.2307+294_2307+301dup	NP_001369725.1:n.2307+294_2307+301dup
NM_001382797.1:c.2209-422_2209-415dup	NP_001369726.1:n.2209-422_2209-415dup
NM_001382798.1:c.2307+294_2307+301dup	NP_001369727.1:n.2307+294_2307+301dup
NM_001382799.1:c.2127+294_2127+301dup	NP_001369728.1:n.2127+294_2127+301dup
NM_001382800.1:c.2307+294_2307+301dup	NP_001369729.1:n.2307+294_2307+301dup
NM_001382801.1:c.2259+294_2259+301dup	NP_001369730.1:n.2259+294_2259+301dup
NM_001382802.1:c.2049+294_2049+301dup	NP_001369731.1:n.2049+294_2049+301dup
NM_001382803.1:c.2265+294_2265+301dup	NP_001369732.1:n.2265+294_2265+301dup
NM_001382804.1:c.1479+294_1479+301dup	NP_001369733.1:n.1479+294_1479+301dup
NM_001382805.1:c.2208+644_2208+651dup	NP_001369734.1:n.2208+644_2208+651dup
NM_001382806.1:c.1269+294_1269+301dup	NP_001369735.1:n.1269+294_1269+301dup
NM_004448.4:c.2307+294_2307+301dup MANE Select	NP_004439.2:n.2307+294_2307+301dup
NR_110535.2:n.2545+294_2545+301dup