Canonical Allele Identifier: CA625937547

Gene: ERBB2

Linked Data

• gnomAD v2: 17-37880430-G-GGT
• gnomAD v3: 17-39724177-G-GGT
• gnomAD v4: 17-39724177-G-GGT
• MyVariant Identifiers: chr17:g.37880430_37880431insGT (hg19) ; chr17:g.39724177_39724178insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724178_39724179insTG , CM000679.2:g.39724178_39724179insTG	GRCh38
NC_000017.10:g.37880431_37880432insTG , CM000679.1:g.37880431_37880432insTG	GRCh37
NC_000017.9:g.35133957_35133958insTG	NCBI36
NG_007503.1:g.41039_41040insTG , LRG_724:g.41039_41040insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2307+168_2307+169insTG MANE Select	ENSP00000269571.4:n.2307+168_2307+169insTG
ENST00000269571.9:c.2307+168_2307+169insTG	ENSP00000269571.4:n.2307+168_2307+169insTG
ENST00000406381.6:c.2217+168_2217+169insTG	ENSP00000385185.2:n.2217+168_2217+169insTG
ENST00000445658.6:c.1479+168_1479+169insTG	ENSP00000404047.2:n.1479+168_1479+169insTG
ENST00000541774.5:c.2262+168_2262+169insTG	ENSP00000446466.1:n.2262+168_2262+169insTG
ENST00000578373.5:c.*2097+168_*2097+169insTG	ENSP00000463427.1:n.*2097+168_*2097+169insTG
ENST00000580074.1:c.413+168_413+169insTG
ENST00000583038.5:n.3441+168_3441+169insTG
ENST00000584450.5:c.2307+168_2307+169insTG	ENSP00000463714.1:n.2307+168_2307+169insTG
ENST00000584601.5:c.2217+168_2217+169insTG	ENSP00000462438.1:n.2217+168_2217+169insTG
NM_001005862.2:c.2217+168_2217+169insTG , LRG_724t1:c.2217+168_2217+169insTG	NP_001005862.1:n.2217+168_2217+169insTG
NM_001289936.1:c.2262+168_2262+169insTG , LRG_724t4:c.2262+168_2262+169insTG	NP_001276865.1:n.2262+168_2262+169insTG
NM_001289937.1:c.2307+168_2307+169insTG	NP_001276866.1:n.2307+168_2307+169insTG
NM_004448.3:c.2307+168_2307+169insTG , LRG_724t2:c.2307+168_2307+169insTG	NP_004439.2:n.2307+168_2307+169insTG
NR_110535.1:n.2631+168_2631+169insTG
XM_024450641.1:c.2445+168_2445+169insTG	XP_024306409.1:n.2445+168_2445+169insTG
XM_024450642.1:c.2400+168_2400+169insTG	XP_024306410.1:n.2400+168_2400+169insTG
XM_024450643.1:c.2355+168_2355+169insTG	XP_024306411.1:n.2355+168_2355+169insTG
NM_001005862.3:c.2217+168_2217+169insTG	NP_001005862.1:n.2217+168_2217+169insTG
NM_001289936.2:c.2262+168_2262+169insTG	NP_001276865.1:n.2262+168_2262+169insTG
NM_001289937.2:c.2307+168_2307+169insTG	NP_001276866.1:n.2307+168_2307+169insTG
NM_001382782.1:c.2217+168_2217+169insTG	NP_001369711.1:n.2217+168_2217+169insTG
NM_001382783.1:c.2217+168_2217+169insTG	NP_001369712.1:n.2217+168_2217+169insTG
NM_001382784.1:c.2424+168_2424+169insTG	NP_001369713.1:n.2424+168_2424+169insTG
NM_001382785.1:c.2409+168_2409+169insTG	NP_001369714.1:n.2409+168_2409+169insTG
NM_001382786.1:c.2388+168_2388+169insTG	NP_001369715.1:n.2388+168_2388+169insTG
NM_001382787.1:c.2382+168_2382+169insTG	NP_001369716.1:n.2382+168_2382+169insTG
NM_001382788.1:c.2337+168_2337+169insTG	NP_001369717.1:n.2337+168_2337+169insTG
NM_001382789.1:c.2328+168_2328+169insTG	NP_001369718.1:n.2328+168_2328+169insTG
NM_001382790.1:c.2304+168_2304+169insTG	NP_001369719.1:n.2304+168_2304+169insTG
NM_001382791.1:c.2298+168_2298+169insTG	NP_001369720.1:n.2298+168_2298+169insTG
NM_001382792.1:c.2271+168_2271+169insTG	NP_001369721.1:n.2271+168_2271+169insTG
NM_001382793.1:c.2265+168_2265+169insTG	NP_001369722.1:n.2265+168_2265+169insTG
NM_001382794.1:c.2265+168_2265+169insTG	NP_001369723.1:n.2265+168_2265+169insTG
NM_001382795.1:c.2259+168_2259+169insTG	NP_001369724.1:n.2259+168_2259+169insTG
NM_001382796.1:c.2307+168_2307+169insTG	NP_001369725.1:n.2307+168_2307+169insTG
NM_001382797.1:c.2208+518_2208+519insTG	NP_001369726.1:n.2208+518_2208+519insTG
NM_001382798.1:c.2307+168_2307+169insTG	NP_001369727.1:n.2307+168_2307+169insTG
NM_001382799.1:c.2127+168_2127+169insTG	NP_001369728.1:n.2127+168_2127+169insTG
NM_001382800.1:c.2307+168_2307+169insTG	NP_001369729.1:n.2307+168_2307+169insTG
NM_001382801.1:c.2259+168_2259+169insTG	NP_001369730.1:n.2259+168_2259+169insTG
NM_001382802.1:c.2049+168_2049+169insTG	NP_001369731.1:n.2049+168_2049+169insTG
NM_001382803.1:c.2265+168_2265+169insTG	NP_001369732.1:n.2265+168_2265+169insTG
NM_001382804.1:c.1479+168_1479+169insTG	NP_001369733.1:n.1479+168_1479+169insTG
NM_001382805.1:c.2208+518_2208+519insTG	NP_001369734.1:n.2208+518_2208+519insTG
NM_001382806.1:c.1269+168_1269+169insTG	NP_001369735.1:n.1269+168_1269+169insTG
NM_004448.4:c.2307+168_2307+169insTG MANE Select	NP_004439.2:n.2307+168_2307+169insTG
NR_110535.2:n.2545+168_2545+169insTG