Canonical Allele Identifier: CA499890601

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143293239
• MyVariant Identifiers: chr17:g.37884009C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727756C>G , CM000679.2:g.39727756C>G	GRCh38
NC_000017.10:g.37884009C>G , CM000679.1:g.37884009C>G	GRCh37
NC_000017.9:g.35137535C>G	NCBI36
NG_007503.1:g.44617C>G , LRG_724:g.44617C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3480C>G MANE Select	ENSP00000269571.4:p.Ala1160=
ENST00000269571.9:c.3480C>G	ENSP00000269571.4:p.Ala1160=
ENST00000406381.6:c.3390C>G	ENSP00000385185.2:p.Ala1130=
ENST00000445658.6:c.2652C>G	ENSP00000404047.2:p.Ala884=
ENST00000541774.5:c.3435C>G	ENSP00000446466.1:p.Ala1145=
ENST00000578373.5:c.*3270C>G	ENSP00000463427.1:n.*3270C>G
ENST00000584450.5:c.*59C>G	ENSP00000463714.1:n.*59C>G
ENST00000584601.5:c.3390C>G	ENSP00000462438.1:p.Ala1130=
NM_001005862.2:c.3390C>G , LRG_724t1:c.3390C>G	NP_001005862.1:p.Ala1130=
NM_001289936.1:c.3435C>G , LRG_724t4:c.3435C>G	NP_001276865.1:p.Ala1145=
NM_001289937.1:c.*59C>G	NP_001276866.1:n.*59C>G
NM_004448.3:c.3480C>G , LRG_724t2:c.3480C>G	NP_004439.2:p.Ala1160=
NR_110535.1:n.3804C>G
XM_024450641.1:c.3618C>G	XP_024306409.1:p.Ala1206=
XM_024450642.1:c.3573C>G	XP_024306410.1:p.Ala1191=
XM_024450643.1:c.3528C>G	XP_024306411.1:p.Ala1176=
NM_001005862.3:c.3390C>G	NP_001005862.1:p.Ala1130=
NM_001289936.2:c.3435C>G	NP_001276865.1:p.Ala1145=
NM_001289937.2:c.*59C>G	NP_001276866.1:n.*59C>G
NM_001382782.1:c.3390C>G	NP_001369711.1:p.Ala1130=
NM_001382783.1:c.3390C>G	NP_001369712.1:p.Ala1130=
NM_001382784.1:c.3597C>G	NP_001369713.1:p.Ala1199=
NM_001382785.1:c.3582C>G	NP_001369714.1:p.Ala1194=
NM_001382786.1:c.3561C>G	NP_001369715.1:p.Ala1187=
NM_001382787.1:c.3555C>G	NP_001369716.1:p.Ala1185=
NM_001382788.1:c.3510C>G	NP_001369717.1:p.Ala1170=
NM_001382789.1:c.3501C>G	NP_001369718.1:p.Ala1167=
NM_001382790.1:c.3477C>G	NP_001369719.1:p.Ala1159=
NM_001382791.1:c.3471C>G	NP_001369720.1:p.Ala1157=
NM_001382792.1:c.3444C>G	NP_001369721.1:p.Ala1148=
NM_001382793.1:c.3438C>G	NP_001369722.1:p.Ala1146=
NM_001382794.1:c.3438C>G	NP_001369723.1:p.Ala1146=
NM_001382795.1:c.3432C>G	NP_001369724.1:p.Ala1144=
NM_001382796.1:c.3393C>G	NP_001369725.1:p.Ala1131=
NM_001382797.1:c.3381C>G	NP_001369726.1:p.Ala1127=
NM_001382798.1:c.3324C>G	NP_001369727.1:p.Ala1108=
NM_001382799.1:c.3300C>G	NP_001369728.1:p.Ala1100=
NM_001382800.1:c.3294C>G	NP_001369729.1:p.Ala1098=
NM_001382801.1:c.3276C>G	NP_001369730.1:p.Ala1092=
NM_001382802.1:c.3222C>G	NP_001369731.1:p.Ala1074=
NM_001382803.1:c.*59C>G	NP_001369732.1:n.*59C>G
NM_001382804.1:c.2652C>G	NP_001369733.1:p.Ala884=
NM_001382805.1:c.2529C>G	NP_001369734.1:p.Ala843=
NM_001382806.1:c.2442C>G	NP_001369735.1:p.Ala814=
NM_004448.4:c.3480C>G MANE Select	NP_004439.2:p.Ala1160=
NR_110535.2:n.3718C>G