Canonical Allele Identifier: CA399313087

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884019G>T (hg19) ; chr17:g.39727766G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727766G>T , CM000679.2:g.39727766G>T	GRCh38
NC_000017.10:g.37884019G>T , CM000679.1:g.37884019G>T	GRCh37
NC_000017.9:g.35137545G>T	NCBI36
NG_007503.1:g.44627G>T , LRG_724:g.44627G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3490G>T MANE Select	ENSP00000269571.4:p.Gly1164Cys
ENST00000269571.9:c.3490G>T	ENSP00000269571.4:p.Gly1164Cys
ENST00000406381.6:c.3400G>T	ENSP00000385185.2:p.Gly1134Cys
ENST00000445658.6:c.2662G>T	ENSP00000404047.2:p.Gly888Cys
ENST00000541774.5:c.3445G>T	ENSP00000446466.1:p.Gly1149Cys
ENST00000578373.5:c.*3280G>T	ENSP00000463427.1:n.*3280G>T
ENST00000584450.5:c.*69G>T	ENSP00000463714.1:n.*69G>T
ENST00000584601.5:c.3400G>T	ENSP00000462438.1:p.Gly1134Cys
NM_001005862.2:c.3400G>T , LRG_724t1:c.3400G>T	NP_001005862.1:p.Gly1134Cys
NM_001289936.1:c.3445G>T , LRG_724t4:c.3445G>T	NP_001276865.1:p.Gly1149Cys
NM_001289937.1:c.*69G>T	NP_001276866.1:n.*69G>T
NM_004448.3:c.3490G>T , LRG_724t2:c.3490G>T	NP_004439.2:p.Gly1164Cys
NR_110535.1:n.3814G>T
XM_024450641.1:c.3628G>T	XP_024306409.1:p.Gly1210Cys
XM_024450642.1:c.3583G>T	XP_024306410.1:p.Gly1195Cys
XM_024450643.1:c.3538G>T	XP_024306411.1:p.Gly1180Cys
NM_001005862.3:c.3400G>T	NP_001005862.1:p.Gly1134Cys
NM_001289936.2:c.3445G>T	NP_001276865.1:p.Gly1149Cys
NM_001289937.2:c.*69G>T	NP_001276866.1:n.*69G>T
NM_001382782.1:c.3400G>T	NP_001369711.1:p.Gly1134Cys
NM_001382783.1:c.3400G>T	NP_001369712.1:p.Gly1134Cys
NM_001382784.1:c.3607G>T	NP_001369713.1:p.Gly1203Cys
NM_001382785.1:c.3592G>T	NP_001369714.1:p.Gly1198Cys
NM_001382786.1:c.3571G>T	NP_001369715.1:p.Gly1191Cys
NM_001382787.1:c.3565G>T	NP_001369716.1:p.Gly1189Cys
NM_001382788.1:c.3520G>T	NP_001369717.1:p.Gly1174Cys
NM_001382789.1:c.3511G>T	NP_001369718.1:p.Gly1171Cys
NM_001382790.1:c.3487G>T	NP_001369719.1:p.Gly1163Cys
NM_001382791.1:c.3481G>T	NP_001369720.1:p.Gly1161Cys
NM_001382792.1:c.3454G>T	NP_001369721.1:p.Gly1152Cys
NM_001382793.1:c.3448G>T	NP_001369722.1:p.Gly1150Cys
NM_001382794.1:c.3448G>T	NP_001369723.1:p.Gly1150Cys
NM_001382795.1:c.3442G>T	NP_001369724.1:p.Gly1148Cys
NM_001382796.1:c.3403G>T	NP_001369725.1:p.Gly1135Cys
NM_001382797.1:c.3391G>T	NP_001369726.1:p.Gly1131Cys
NM_001382798.1:c.3334G>T	NP_001369727.1:p.Gly1112Cys
NM_001382799.1:c.3310G>T	NP_001369728.1:p.Gly1104Cys
NM_001382800.1:c.3304G>T	NP_001369729.1:p.Gly1102Cys
NM_001382801.1:c.3286G>T	NP_001369730.1:p.Gly1096Cys
NM_001382802.1:c.3232G>T	NP_001369731.1:p.Gly1078Cys
NM_001382803.1:c.*69G>T	NP_001369732.1:n.*69G>T
NM_001382804.1:c.2662G>T	NP_001369733.1:p.Gly888Cys
NM_001382805.1:c.2539G>T	NP_001369734.1:p.Gly847Cys
NM_001382806.1:c.2452G>T	NP_001369735.1:p.Gly818Cys
NM_004448.4:c.3490G>T MANE Select	NP_004439.2:p.Gly1164Cys
NR_110535.2:n.3728G>T