Canonical Allele Identifier: CA399313885

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143306548
• MyVariant Identifiers: chr17:g.37884129G>T (hg19) ; chr17:g.39727876G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727876G>T , CM000679.2:g.39727876G>T	GRCh38
NC_000017.10:g.37884129G>T , CM000679.1:g.37884129G>T	GRCh37
NC_000017.9:g.35137655G>T	NCBI36
NG_007503.1:g.44737G>T , LRG_724:g.44737G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3600G>T MANE Select	ENSP00000269571.4:p.Gln1200His
ENST00000269571.9:c.3600G>T	ENSP00000269571.4:p.Gln1200His
ENST00000406381.6:c.3510G>T	ENSP00000385185.2:p.Gln1170His
ENST00000445658.6:c.2772G>T	ENSP00000404047.2:p.Gln924His
ENST00000541774.5:c.3555G>T	ENSP00000446466.1:p.Gln1185His
ENST00000578373.5:c.*3390G>T	ENSP00000463427.1:n.*3390G>T
ENST00000584450.5:c.*179G>T	ENSP00000463714.1:n.*179G>T
ENST00000584601.5:c.3510G>T	ENSP00000462438.1:p.Gln1170His
NM_001005862.2:c.3510G>T , LRG_724t1:c.3510G>T	NP_001005862.1:p.Gln1170His
NM_001289936.1:c.3555G>T , LRG_724t4:c.3555G>T	NP_001276865.1:p.Gln1185His
NM_001289937.1:c.*179G>T	NP_001276866.1:n.*179G>T
NM_004448.3:c.3600G>T , LRG_724t2:c.3600G>T	NP_004439.2:p.Gln1200His
NR_110535.1:n.3924G>T
XM_024450641.1:c.3738G>T	XP_024306409.1:p.Gln1246His
XM_024450642.1:c.3693G>T	XP_024306410.1:p.Gln1231His
XM_024450643.1:c.3648G>T	XP_024306411.1:p.Gln1216His
NM_001005862.3:c.3510G>T	NP_001005862.1:p.Gln1170His
NM_001289936.2:c.3555G>T	NP_001276865.1:p.Gln1185His
NM_001289937.2:c.*179G>T	NP_001276866.1:n.*179G>T
NM_001382782.1:c.3510G>T	NP_001369711.1:p.Gln1170His
NM_001382783.1:c.3510G>T	NP_001369712.1:p.Gln1170His
NM_001382784.1:c.3717G>T	NP_001369713.1:p.Gln1239His
NM_001382785.1:c.3702G>T	NP_001369714.1:p.Gln1234His
NM_001382786.1:c.3681G>T	NP_001369715.1:p.Gln1227His
NM_001382787.1:c.3675G>T	NP_001369716.1:p.Gln1225His
NM_001382788.1:c.3630G>T	NP_001369717.1:p.Gln1210His
NM_001382789.1:c.3621G>T	NP_001369718.1:p.Gln1207His
NM_001382790.1:c.3597G>T	NP_001369719.1:p.Gln1199His
NM_001382791.1:c.3591G>T	NP_001369720.1:p.Gln1197His
NM_001382792.1:c.3564G>T	NP_001369721.1:p.Gln1188His
NM_001382793.1:c.3558G>T	NP_001369722.1:p.Gln1186His
NM_001382794.1:c.3558G>T	NP_001369723.1:p.Gln1186His
NM_001382795.1:c.3552G>T	NP_001369724.1:p.Gln1184His
NM_001382796.1:c.3513G>T	NP_001369725.1:p.Gln1171His
NM_001382797.1:c.3501G>T	NP_001369726.1:p.Gln1167His
NM_001382798.1:c.3444G>T	NP_001369727.1:p.Gln1148His
NM_001382799.1:c.3420G>T	NP_001369728.1:p.Gln1140His
NM_001382800.1:c.3414G>T	NP_001369729.1:p.Gln1138His
NM_001382801.1:c.3396G>T	NP_001369730.1:p.Gln1132His
NM_001382802.1:c.3342G>T	NP_001369731.1:p.Gln1114His
NM_001382803.1:c.*179G>T	NP_001369732.1:n.*179G>T
NM_001382804.1:c.2772G>T	NP_001369733.1:p.Gln924His
NM_001382805.1:c.2649G>T	NP_001369734.1:p.Gln883His
NM_001382806.1:c.2562G>T	NP_001369735.1:p.Gln854His
NM_004448.4:c.3600G>T MANE Select	NP_004439.2:p.Gln1200His
NR_110535.2:n.3838G>T