Canonical Allele Identifier: CA399314460

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884203A>C (hg19) ; chr17:g.39727950A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727950A>C , CM000679.2:g.39727950A>C	GRCh38
NC_000017.10:g.37884203A>C , CM000679.1:g.37884203A>C	GRCh37
NC_000017.9:g.35137729A>C	NCBI36
NG_007503.1:g.44811A>C , LRG_724:g.44811A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3674A>C MANE Select	ENSP00000269571.4:p.Gln1225Pro
ENST00000269571.9:c.3674A>C	ENSP00000269571.4:p.Gln1225Pro
ENST00000406381.6:c.3584A>C	ENSP00000385185.2:p.Gln1195Pro
ENST00000445658.6:c.2846A>C	ENSP00000404047.2:p.Gln949Pro
ENST00000541774.5:c.3629A>C	ENSP00000446466.1:p.Gln1210Pro
ENST00000578373.5:c.*3464A>C	ENSP00000463427.1:n.*3464A>C
ENST00000584450.5:c.*253A>C	ENSP00000463714.1:n.*253A>C
ENST00000584601.5:c.3584A>C	ENSP00000462438.1:p.Gln1195Pro
NM_001005862.2:c.3584A>C , LRG_724t1:c.3584A>C	NP_001005862.1:p.Gln1195Pro
NM_001289936.1:c.3629A>C , LRG_724t4:c.3629A>C	NP_001276865.1:p.Gln1210Pro
NM_001289937.1:c.*253A>C	NP_001276866.1:n.*253A>C
NM_004448.3:c.3674A>C , LRG_724t2:c.3674A>C	NP_004439.2:p.Gln1225Pro
NR_110535.1:n.3998A>C
XM_024450641.1:c.3812A>C	XP_024306409.1:p.Gln1271Pro
XM_024450642.1:c.3767A>C	XP_024306410.1:p.Gln1256Pro
XM_024450643.1:c.3722A>C	XP_024306411.1:p.Gln1241Pro
NM_001005862.3:c.3584A>C	NP_001005862.1:p.Gln1195Pro
NM_001289936.2:c.3629A>C	NP_001276865.1:p.Gln1210Pro
NM_001289937.2:c.*253A>C	NP_001276866.1:n.*253A>C
NM_001382782.1:c.3584A>C	NP_001369711.1:p.Gln1195Pro
NM_001382783.1:c.3584A>C	NP_001369712.1:p.Gln1195Pro
NM_001382784.1:c.3791A>C	NP_001369713.1:p.Gln1264Pro
NM_001382785.1:c.3776A>C	NP_001369714.1:p.Gln1259Pro
NM_001382786.1:c.3755A>C	NP_001369715.1:p.Gln1252Pro
NM_001382787.1:c.3749A>C	NP_001369716.1:p.Gln1250Pro
NM_001382788.1:c.3704A>C	NP_001369717.1:p.Gln1235Pro
NM_001382789.1:c.3695A>C	NP_001369718.1:p.Gln1232Pro
NM_001382790.1:c.3671A>C	NP_001369719.1:p.Gln1224Pro
NM_001382791.1:c.3665A>C	NP_001369720.1:p.Gln1222Pro
NM_001382792.1:c.3638A>C	NP_001369721.1:p.Gln1213Pro
NM_001382793.1:c.3632A>C	NP_001369722.1:p.Gln1211Pro
NM_001382794.1:c.3632A>C	NP_001369723.1:p.Gln1211Pro
NM_001382795.1:c.3626A>C	NP_001369724.1:p.Gln1209Pro
NM_001382796.1:c.3587A>C	NP_001369725.1:p.Gln1196Pro
NM_001382797.1:c.3575A>C	NP_001369726.1:p.Gln1192Pro
NM_001382798.1:c.3518A>C	NP_001369727.1:p.Gln1173Pro
NM_001382799.1:c.3494A>C	NP_001369728.1:p.Gln1165Pro
NM_001382800.1:c.3488A>C	NP_001369729.1:p.Gln1163Pro
NM_001382801.1:c.3470A>C	NP_001369730.1:p.Gln1157Pro
NM_001382802.1:c.3416A>C	NP_001369731.1:p.Gln1139Pro
NM_001382803.1:c.*253A>C	NP_001369732.1:n.*253A>C
NM_001382804.1:c.2846A>C	NP_001369733.1:p.Gln949Pro
NM_001382805.1:c.2723A>C	NP_001369734.1:p.Gln908Pro
NM_001382806.1:c.2636A>C	NP_001369735.1:p.Gln879Pro
NM_004448.4:c.3674A>C MANE Select	NP_004439.2:p.Gln1225Pro
NR_110535.2:n.3912A>C