Canonical Allele Identifier: CA399313394

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143299089
• MyVariant Identifiers: chr17:g.37884064G>C (hg19) ; chr17:g.39727811G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727811G>C , CM000679.2:g.39727811G>C	GRCh38
NC_000017.10:g.37884064G>C , CM000679.1:g.37884064G>C	GRCh37
NC_000017.9:g.35137590G>C	NCBI36
NG_007503.1:g.44672G>C , LRG_724:g.44672G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3535G>C MANE Select	ENSP00000269571.4:p.Gly1179Arg
ENST00000269571.9:c.3535G>C	ENSP00000269571.4:p.Gly1179Arg
ENST00000406381.6:c.3445G>C	ENSP00000385185.2:p.Gly1149Arg
ENST00000445658.6:c.2707G>C	ENSP00000404047.2:p.Gly903Arg
ENST00000541774.5:c.3490G>C	ENSP00000446466.1:p.Gly1164Arg
ENST00000578373.5:c.*3325G>C	ENSP00000463427.1:n.*3325G>C
ENST00000584450.5:c.*114G>C	ENSP00000463714.1:n.*114G>C
ENST00000584601.5:c.3445G>C	ENSP00000462438.1:p.Gly1149Arg
NM_001005862.2:c.3445G>C , LRG_724t1:c.3445G>C	NP_001005862.1:p.Gly1149Arg
NM_001289936.1:c.3490G>C , LRG_724t4:c.3490G>C	NP_001276865.1:p.Gly1164Arg
NM_001289937.1:c.*114G>C	NP_001276866.1:n.*114G>C
NM_004448.3:c.3535G>C , LRG_724t2:c.3535G>C	NP_004439.2:p.Gly1179Arg
NR_110535.1:n.3859G>C
XM_024450641.1:c.3673G>C	XP_024306409.1:p.Gly1225Arg
XM_024450642.1:c.3628G>C	XP_024306410.1:p.Gly1210Arg
XM_024450643.1:c.3583G>C	XP_024306411.1:p.Gly1195Arg
NM_001005862.3:c.3445G>C	NP_001005862.1:p.Gly1149Arg
NM_001289936.2:c.3490G>C	NP_001276865.1:p.Gly1164Arg
NM_001289937.2:c.*114G>C	NP_001276866.1:n.*114G>C
NM_001382782.1:c.3445G>C	NP_001369711.1:p.Gly1149Arg
NM_001382783.1:c.3445G>C	NP_001369712.1:p.Gly1149Arg
NM_001382784.1:c.3652G>C	NP_001369713.1:p.Gly1218Arg
NM_001382785.1:c.3637G>C	NP_001369714.1:p.Gly1213Arg
NM_001382786.1:c.3616G>C	NP_001369715.1:p.Gly1206Arg
NM_001382787.1:c.3610G>C	NP_001369716.1:p.Gly1204Arg
NM_001382788.1:c.3565G>C	NP_001369717.1:p.Gly1189Arg
NM_001382789.1:c.3556G>C	NP_001369718.1:p.Gly1186Arg
NM_001382790.1:c.3532G>C	NP_001369719.1:p.Gly1178Arg
NM_001382791.1:c.3526G>C	NP_001369720.1:p.Gly1176Arg
NM_001382792.1:c.3499G>C	NP_001369721.1:p.Gly1167Arg
NM_001382793.1:c.3493G>C	NP_001369722.1:p.Gly1165Arg
NM_001382794.1:c.3493G>C	NP_001369723.1:p.Gly1165Arg
NM_001382795.1:c.3487G>C	NP_001369724.1:p.Gly1163Arg
NM_001382796.1:c.3448G>C	NP_001369725.1:p.Gly1150Arg
NM_001382797.1:c.3436G>C	NP_001369726.1:p.Gly1146Arg
NM_001382798.1:c.3379G>C	NP_001369727.1:p.Gly1127Arg
NM_001382799.1:c.3355G>C	NP_001369728.1:p.Gly1119Arg
NM_001382800.1:c.3349G>C	NP_001369729.1:p.Gly1117Arg
NM_001382801.1:c.3331G>C	NP_001369730.1:p.Gly1111Arg
NM_001382802.1:c.3277G>C	NP_001369731.1:p.Gly1093Arg
NM_001382803.1:c.*114G>C	NP_001369732.1:n.*114G>C
NM_001382804.1:c.2707G>C	NP_001369733.1:p.Gly903Arg
NM_001382805.1:c.2584G>C	NP_001369734.1:p.Gly862Arg
NM_001382806.1:c.2497G>C	NP_001369735.1:p.Gly833Arg
NM_004448.4:c.3535G>C MANE Select	NP_004439.2:p.Gly1179Arg
NR_110535.2:n.3773G>C