Canonical Allele Identifier: CA499890786

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143306548
• gnomAD v4: 17-39727876-G-A
• MyVariant Identifiers: chr17:g.37884129G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3600G>A MANE Select	ENSP00000269571.4:p.Gln1200=
ENST00000269571.9:c.3600G>A	ENSP00000269571.4:p.Gln1200=
ENST00000406381.6:c.3510G>A	ENSP00000385185.2:p.Gln1170=
ENST00000445658.6:c.2772G>A	ENSP00000404047.2:p.Gln924=
ENST00000541774.5:c.3555G>A	ENSP00000446466.1:p.Gln1185=
ENST00000578373.5:c.*3390G>A	ENSP00000463427.1:n.*3390G>A
ENST00000584450.5:c.*179G>A	ENSP00000463714.1:n.*179G>A
ENST00000584601.5:c.3510G>A	ENSP00000462438.1:p.Gln1170=
NM_001005862.2:c.3510G>A , LRG_724t1:c.3510G>A	NP_001005862.1:p.Gln1170=
NM_001289936.1:c.3555G>A , LRG_724t4:c.3555G>A	NP_001276865.1:p.Gln1185=
NM_001289937.1:c.*179G>A	NP_001276866.1:n.*179G>A
NM_004448.3:c.3600G>A , LRG_724t2:c.3600G>A	NP_004439.2:p.Gln1200=
NR_110535.1:n.3924G>A
XM_024450641.1:c.3738G>A	XP_024306409.1:p.Gln1246=
XM_024450642.1:c.3693G>A	XP_024306410.1:p.Gln1231=
XM_024450643.1:c.3648G>A	XP_024306411.1:p.Gln1216=
NM_001005862.3:c.3510G>A	NP_001005862.1:p.Gln1170=
NM_001289936.2:c.3555G>A	NP_001276865.1:p.Gln1185=
NM_001289937.2:c.*179G>A	NP_001276866.1:n.*179G>A
NM_001382782.1:c.3510G>A	NP_001369711.1:p.Gln1170=
NM_001382783.1:c.3510G>A	NP_001369712.1:p.Gln1170=
NM_001382784.1:c.3717G>A	NP_001369713.1:p.Gln1239=
NM_001382785.1:c.3702G>A	NP_001369714.1:p.Gln1234=
NM_001382786.1:c.3681G>A	NP_001369715.1:p.Gln1227=
NM_001382787.1:c.3675G>A	NP_001369716.1:p.Gln1225=
NM_001382788.1:c.3630G>A	NP_001369717.1:p.Gln1210=
NM_001382789.1:c.3621G>A	NP_001369718.1:p.Gln1207=
NM_001382790.1:c.3597G>A	NP_001369719.1:p.Gln1199=
NM_001382791.1:c.3591G>A	NP_001369720.1:p.Gln1197=
NM_001382792.1:c.3564G>A	NP_001369721.1:p.Gln1188=
NM_001382793.1:c.3558G>A	NP_001369722.1:p.Gln1186=
NM_001382794.1:c.3558G>A	NP_001369723.1:p.Gln1186=
NM_001382795.1:c.3552G>A	NP_001369724.1:p.Gln1184=
NM_001382796.1:c.3513G>A	NP_001369725.1:p.Gln1171=
NM_001382797.1:c.3501G>A	NP_001369726.1:p.Gln1167=
NM_001382798.1:c.3444G>A	NP_001369727.1:p.Gln1148=
NM_001382799.1:c.3420G>A	NP_001369728.1:p.Gln1140=
NM_001382800.1:c.3414G>A	NP_001369729.1:p.Gln1138=
NM_001382801.1:c.3396G>A	NP_001369730.1:p.Gln1132=
NM_001382802.1:c.3342G>A	NP_001369731.1:p.Gln1114=
NM_001382803.1:c.*179G>A	NP_001369732.1:n.*179G>A
NM_001382804.1:c.2772G>A	NP_001369733.1:p.Gln924=
NM_001382805.1:c.2649G>A	NP_001369734.1:p.Gln883=
NM_001382806.1:c.2562G>A	NP_001369735.1:p.Gln854=
NM_004448.4:c.3600G>A MANE Select	NP_004439.2:p.Gln1200=
NR_110535.2:n.3838G>A