Canonical Allele Identifier: CA399312847

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143287690
• MyVariant Identifiers: chr17:g.37883954A>G (hg19) ; chr17:g.39727701A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727701A>G , CM000679.2:g.39727701A>G	GRCh38
NC_000017.10:g.37883954A>G , CM000679.1:g.37883954A>G	GRCh37
NC_000017.9:g.35137480A>G	NCBI36
NG_007503.1:g.44562A>G , LRG_724:g.44562A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.3425A>G MANE Select	ENSP00000269571.4:p.Gln1142Arg
ENST00000269571.9:c.3425A>G	ENSP00000269571.4:p.Gln1142Arg
ENST00000406381.6:c.3335A>G	ENSP00000385185.2:p.Gln1112Arg
ENST00000445658.6:c.2597A>G	ENSP00000404047.2:p.Gln866Arg
ENST00000541774.5:c.3380A>G	ENSP00000446466.1:p.Gln1127Arg
ENST00000578373.5:c.*3215A>G	ENSP00000463427.1:n.*3215A>G
ENST00000584450.5:c.*4A>G	ENSP00000463714.1:n.*4A>G
ENST00000584601.5:c.3335A>G	ENSP00000462438.1:p.Gln1112Arg
NM_001005862.2:c.3335A>G , LRG_724t1:c.3335A>G	NP_001005862.1:p.Gln1112Arg
NM_001289936.1:c.3380A>G , LRG_724t4:c.3380A>G	NP_001276865.1:p.Gln1127Arg
NM_001289937.1:c.*4A>G	NP_001276866.1:n.*4A>G
NM_004448.3:c.3425A>G , LRG_724t2:c.3425A>G	NP_004439.2:p.Gln1142Arg
NR_110535.1:n.3749A>G
XM_024450641.1:c.3563A>G	XP_024306409.1:p.Gln1188Arg
XM_024450642.1:c.3518A>G	XP_024306410.1:p.Gln1173Arg
XM_024450643.1:c.3473A>G	XP_024306411.1:p.Gln1158Arg
NM_001005862.3:c.3335A>G	NP_001005862.1:p.Gln1112Arg
NM_001289936.2:c.3380A>G	NP_001276865.1:p.Gln1127Arg
NM_001289937.2:c.*4A>G	NP_001276866.1:n.*4A>G
NM_001382782.1:c.3335A>G	NP_001369711.1:p.Gln1112Arg
NM_001382783.1:c.3335A>G	NP_001369712.1:p.Gln1112Arg
NM_001382784.1:c.3542A>G	NP_001369713.1:p.Gln1181Arg
NM_001382785.1:c.3527A>G	NP_001369714.1:p.Gln1176Arg
NM_001382786.1:c.3506A>G	NP_001369715.1:p.Gln1169Arg
NM_001382787.1:c.3500A>G	NP_001369716.1:p.Gln1167Arg
NM_001382788.1:c.3455A>G	NP_001369717.1:p.Gln1152Arg
NM_001382789.1:c.3446A>G	NP_001369718.1:p.Gln1149Arg
NM_001382790.1:c.3422A>G	NP_001369719.1:p.Gln1141Arg
NM_001382791.1:c.3416A>G	NP_001369720.1:p.Gln1139Arg
NM_001382792.1:c.3389A>G	NP_001369721.1:p.Gln1130Arg
NM_001382793.1:c.3383A>G	NP_001369722.1:p.Gln1128Arg
NM_001382794.1:c.3383A>G	NP_001369723.1:p.Gln1128Arg
NM_001382795.1:c.3377A>G	NP_001369724.1:p.Gln1126Arg
NM_001382796.1:c.3338A>G	NP_001369725.1:p.Gln1113Arg
NM_001382797.1:c.3326A>G	NP_001369726.1:p.Gln1109Arg
NM_001382798.1:c.3269A>G	NP_001369727.1:p.Gln1090Arg
NM_001382799.1:c.3245A>G	NP_001369728.1:p.Gln1082Arg
NM_001382800.1:c.3239A>G	NP_001369729.1:p.Gln1080Arg
NM_001382801.1:c.3221A>G	NP_001369730.1:p.Gln1074Arg
NM_001382802.1:c.3167A>G	NP_001369731.1:p.Gln1056Arg
NM_001382803.1:c.*4A>G	NP_001369732.1:n.*4A>G
NM_001382804.1:c.2597A>G	NP_001369733.1:p.Gln866Arg
NM_001382805.1:c.2474A>G	NP_001369734.1:p.Gln825Arg
NM_001382806.1:c.2387A>G	NP_001369735.1:p.Gln796Arg
NM_004448.4:c.3425A>G MANE Select	NP_004439.2:p.Gln1142Arg
NR_110535.2:n.3663A>G