Canonical Allele Identifier: CA499890500

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883967G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727714G>C , CM000679.2:g.39727714G>C	GRCh38
NC_000017.10:g.37883967G>C , CM000679.1:g.37883967G>C	GRCh37
NC_000017.9:g.35137493G>C	NCBI36
NG_007503.1:g.44575G>C , LRG_724:g.44575G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3438G>C MANE Select	ENSP00000269571.4:p.Arg1146=
ENST00000269571.9:c.3438G>C	ENSP00000269571.4:p.Arg1146=
ENST00000406381.6:c.3348G>C	ENSP00000385185.2:p.Arg1116=
ENST00000445658.6:c.2610G>C	ENSP00000404047.2:p.Arg870=
ENST00000541774.5:c.3393G>C	ENSP00000446466.1:p.Arg1131=
ENST00000578373.5:c.*3228G>C	ENSP00000463427.1:n.*3228G>C
ENST00000584450.5:c.*17G>C	ENSP00000463714.1:n.*17G>C
ENST00000584601.5:c.3348G>C	ENSP00000462438.1:p.Arg1116=
NM_001005862.2:c.3348G>C , LRG_724t1:c.3348G>C	NP_001005862.1:p.Arg1116=
NM_001289936.1:c.3393G>C , LRG_724t4:c.3393G>C	NP_001276865.1:p.Arg1131=
NM_001289937.1:c.*17G>C	NP_001276866.1:n.*17G>C
NM_004448.3:c.3438G>C , LRG_724t2:c.3438G>C	NP_004439.2:p.Arg1146=
NR_110535.1:n.3762G>C
XM_024450641.1:c.3576G>C	XP_024306409.1:p.Arg1192=
XM_024450642.1:c.3531G>C	XP_024306410.1:p.Arg1177=
XM_024450643.1:c.3486G>C	XP_024306411.1:p.Arg1162=
NM_001005862.3:c.3348G>C	NP_001005862.1:p.Arg1116=
NM_001289936.2:c.3393G>C	NP_001276865.1:p.Arg1131=
NM_001289937.2:c.*17G>C	NP_001276866.1:n.*17G>C
NM_001382782.1:c.3348G>C	NP_001369711.1:p.Arg1116=
NM_001382783.1:c.3348G>C	NP_001369712.1:p.Arg1116=
NM_001382784.1:c.3555G>C	NP_001369713.1:p.Arg1185=
NM_001382785.1:c.3540G>C	NP_001369714.1:p.Arg1180=
NM_001382786.1:c.3519G>C	NP_001369715.1:p.Arg1173=
NM_001382787.1:c.3513G>C	NP_001369716.1:p.Arg1171=
NM_001382788.1:c.3468G>C	NP_001369717.1:p.Arg1156=
NM_001382789.1:c.3459G>C	NP_001369718.1:p.Arg1153=
NM_001382790.1:c.3435G>C	NP_001369719.1:p.Arg1145=
NM_001382791.1:c.3429G>C	NP_001369720.1:p.Arg1143=
NM_001382792.1:c.3402G>C	NP_001369721.1:p.Arg1134=
NM_001382793.1:c.3396G>C	NP_001369722.1:p.Arg1132=
NM_001382794.1:c.3396G>C	NP_001369723.1:p.Arg1132=
NM_001382795.1:c.3390G>C	NP_001369724.1:p.Arg1130=
NM_001382796.1:c.3351G>C	NP_001369725.1:p.Arg1117=
NM_001382797.1:c.3339G>C	NP_001369726.1:p.Arg1113=
NM_001382798.1:c.3282G>C	NP_001369727.1:p.Arg1094=
NM_001382799.1:c.3258G>C	NP_001369728.1:p.Arg1086=
NM_001382800.1:c.3252G>C	NP_001369729.1:p.Arg1084=
NM_001382801.1:c.3234G>C	NP_001369730.1:p.Arg1078=
NM_001382802.1:c.3180G>C	NP_001369731.1:p.Arg1060=
NM_001382803.1:c.*17G>C	NP_001369732.1:n.*17G>C
NM_001382804.1:c.2610G>C	NP_001369733.1:p.Arg870=
NM_001382805.1:c.2487G>C	NP_001369734.1:p.Arg829=
NM_001382806.1:c.2400G>C	NP_001369735.1:p.Arg800=
NM_004448.4:c.3438G>C MANE Select	NP_004439.2:p.Arg1146=
NR_110535.2:n.3676G>C