Canonical Allele Identifier: CA399314408

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884197G>T (hg19) ; chr17:g.39727944G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727944G>T , CM000679.2:g.39727944G>T	GRCh38
NC_000017.10:g.37884197G>T , CM000679.1:g.37884197G>T	GRCh37
NC_000017.9:g.35137723G>T	NCBI36
NG_007503.1:g.44805G>T , LRG_724:g.44805G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3668G>T MANE Select	ENSP00000269571.4:p.Trp1223Leu
ENST00000269571.9:c.3668G>T	ENSP00000269571.4:p.Trp1223Leu
ENST00000406381.6:c.3578G>T	ENSP00000385185.2:p.Trp1193Leu
ENST00000445658.6:c.2840G>T	ENSP00000404047.2:p.Trp947Leu
ENST00000541774.5:c.3623G>T	ENSP00000446466.1:p.Trp1208Leu
ENST00000578373.5:c.*3458G>T	ENSP00000463427.1:n.*3458G>T
ENST00000584450.5:c.*247G>T	ENSP00000463714.1:n.*247G>T
ENST00000584601.5:c.3578G>T	ENSP00000462438.1:p.Trp1193Leu
NM_001005862.2:c.3578G>T , LRG_724t1:c.3578G>T	NP_001005862.1:p.Trp1193Leu
NM_001289936.1:c.3623G>T , LRG_724t4:c.3623G>T	NP_001276865.1:p.Trp1208Leu
NM_001289937.1:c.*247G>T	NP_001276866.1:n.*247G>T
NM_004448.3:c.3668G>T , LRG_724t2:c.3668G>T	NP_004439.2:p.Trp1223Leu
NR_110535.1:n.3992G>T
XM_024450641.1:c.3806G>T	XP_024306409.1:p.Trp1269Leu
XM_024450642.1:c.3761G>T	XP_024306410.1:p.Trp1254Leu
XM_024450643.1:c.3716G>T	XP_024306411.1:p.Trp1239Leu
NM_001005862.3:c.3578G>T	NP_001005862.1:p.Trp1193Leu
NM_001289936.2:c.3623G>T	NP_001276865.1:p.Trp1208Leu
NM_001289937.2:c.*247G>T	NP_001276866.1:n.*247G>T
NM_001382782.1:c.3578G>T	NP_001369711.1:p.Trp1193Leu
NM_001382783.1:c.3578G>T	NP_001369712.1:p.Trp1193Leu
NM_001382784.1:c.3785G>T	NP_001369713.1:p.Trp1262Leu
NM_001382785.1:c.3770G>T	NP_001369714.1:p.Trp1257Leu
NM_001382786.1:c.3749G>T	NP_001369715.1:p.Trp1250Leu
NM_001382787.1:c.3743G>T	NP_001369716.1:p.Trp1248Leu
NM_001382788.1:c.3698G>T	NP_001369717.1:p.Trp1233Leu
NM_001382789.1:c.3689G>T	NP_001369718.1:p.Trp1230Leu
NM_001382790.1:c.3665G>T	NP_001369719.1:p.Trp1222Leu
NM_001382791.1:c.3659G>T	NP_001369720.1:p.Trp1220Leu
NM_001382792.1:c.3632G>T	NP_001369721.1:p.Trp1211Leu
NM_001382793.1:c.3626G>T	NP_001369722.1:p.Trp1209Leu
NM_001382794.1:c.3626G>T	NP_001369723.1:p.Trp1209Leu
NM_001382795.1:c.3620G>T	NP_001369724.1:p.Trp1207Leu
NM_001382796.1:c.3581G>T	NP_001369725.1:p.Trp1194Leu
NM_001382797.1:c.3569G>T	NP_001369726.1:p.Trp1190Leu
NM_001382798.1:c.3512G>T	NP_001369727.1:p.Trp1171Leu
NM_001382799.1:c.3488G>T	NP_001369728.1:p.Trp1163Leu
NM_001382800.1:c.3482G>T	NP_001369729.1:p.Trp1161Leu
NM_001382801.1:c.3464G>T	NP_001369730.1:p.Trp1155Leu
NM_001382802.1:c.3410G>T	NP_001369731.1:p.Trp1137Leu
NM_001382803.1:c.*247G>T	NP_001369732.1:n.*247G>T
NM_001382804.1:c.2840G>T	NP_001369733.1:p.Trp947Leu
NM_001382805.1:c.2717G>T	NP_001369734.1:p.Trp906Leu
NM_001382806.1:c.2630G>T	NP_001369735.1:p.Trp877Leu
NM_004448.4:c.3668G>T MANE Select	NP_004439.2:p.Trp1223Leu
NR_110535.2:n.3906G>T