Canonical Allele Identifier: CA399313527

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884082T>G (hg19) ; chr17:g.39727829T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727829T>G , CM000679.2:g.39727829T>G	GRCh38
NC_000017.10:g.37884082T>G , CM000679.1:g.37884082T>G	GRCh37
NC_000017.9:g.35137608T>G	NCBI36
NG_007503.1:g.44690T>G , LRG_724:g.44690T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3553T>G MANE Select	ENSP00000269571.4:p.Phe1185Val
ENST00000269571.9:c.3553T>G	ENSP00000269571.4:p.Phe1185Val
ENST00000406381.6:c.3463T>G	ENSP00000385185.2:p.Phe1155Val
ENST00000445658.6:c.2725T>G	ENSP00000404047.2:p.Phe909Val
ENST00000541774.5:c.3508T>G	ENSP00000446466.1:p.Phe1170Val
ENST00000578373.5:c.*3343T>G	ENSP00000463427.1:n.*3343T>G
ENST00000584450.5:c.*132T>G	ENSP00000463714.1:n.*132T>G
ENST00000584601.5:c.3463T>G	ENSP00000462438.1:p.Phe1155Val
NM_001005862.2:c.3463T>G , LRG_724t1:c.3463T>G	NP_001005862.1:p.Phe1155Val
NM_001289936.1:c.3508T>G , LRG_724t4:c.3508T>G	NP_001276865.1:p.Phe1170Val
NM_001289937.1:c.*132T>G	NP_001276866.1:n.*132T>G
NM_004448.3:c.3553T>G , LRG_724t2:c.3553T>G	NP_004439.2:p.Phe1185Val
NR_110535.1:n.3877T>G
XM_024450641.1:c.3691T>G	XP_024306409.1:p.Phe1231Val
XM_024450642.1:c.3646T>G	XP_024306410.1:p.Phe1216Val
XM_024450643.1:c.3601T>G	XP_024306411.1:p.Phe1201Val
NM_001005862.3:c.3463T>G	NP_001005862.1:p.Phe1155Val
NM_001289936.2:c.3508T>G	NP_001276865.1:p.Phe1170Val
NM_001289937.2:c.*132T>G	NP_001276866.1:n.*132T>G
NM_001382782.1:c.3463T>G	NP_001369711.1:p.Phe1155Val
NM_001382783.1:c.3463T>G	NP_001369712.1:p.Phe1155Val
NM_001382784.1:c.3670T>G	NP_001369713.1:p.Phe1224Val
NM_001382785.1:c.3655T>G	NP_001369714.1:p.Phe1219Val
NM_001382786.1:c.3634T>G	NP_001369715.1:p.Phe1212Val
NM_001382787.1:c.3628T>G	NP_001369716.1:p.Phe1210Val
NM_001382788.1:c.3583T>G	NP_001369717.1:p.Phe1195Val
NM_001382789.1:c.3574T>G	NP_001369718.1:p.Phe1192Val
NM_001382790.1:c.3550T>G	NP_001369719.1:p.Phe1184Val
NM_001382791.1:c.3544T>G	NP_001369720.1:p.Phe1182Val
NM_001382792.1:c.3517T>G	NP_001369721.1:p.Phe1173Val
NM_001382793.1:c.3511T>G	NP_001369722.1:p.Phe1171Val
NM_001382794.1:c.3511T>G	NP_001369723.1:p.Phe1171Val
NM_001382795.1:c.3505T>G	NP_001369724.1:p.Phe1169Val
NM_001382796.1:c.3466T>G	NP_001369725.1:p.Phe1156Val
NM_001382797.1:c.3454T>G	NP_001369726.1:p.Phe1152Val
NM_001382798.1:c.3397T>G	NP_001369727.1:p.Phe1133Val
NM_001382799.1:c.3373T>G	NP_001369728.1:p.Phe1125Val
NM_001382800.1:c.3367T>G	NP_001369729.1:p.Phe1123Val
NM_001382801.1:c.3349T>G	NP_001369730.1:p.Phe1117Val
NM_001382802.1:c.3295T>G	NP_001369731.1:p.Phe1099Val
NM_001382803.1:c.*132T>G	NP_001369732.1:n.*132T>G
NM_001382804.1:c.2725T>G	NP_001369733.1:p.Phe909Val
NM_001382805.1:c.2602T>G	NP_001369734.1:p.Phe868Val
NM_001382806.1:c.2515T>G	NP_001369735.1:p.Phe839Val
NM_004448.4:c.3553T>G MANE Select	NP_004439.2:p.Phe1185Val
NR_110535.2:n.3791T>G