Canonical Allele Identifier: CA499890749

Gene: ERBB2

Linked Data

• dbSNP Id: rs149815705
• MyVariant Identifiers: chr17:g.37884099C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727846C>G , CM000679.2:g.39727846C>G	GRCh38
NC_000017.10:g.37884099C>G , CM000679.1:g.37884099C>G	GRCh37
NC_000017.9:g.35137625C>G	NCBI36
NG_007503.1:g.44707C>G , LRG_724:g.44707C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3570C>G MANE Select	ENSP00000269571.4:p.Ala1190=
ENST00000269571.9:c.3570C>G	ENSP00000269571.4:p.Ala1190=
ENST00000406381.6:c.3480C>G	ENSP00000385185.2:p.Ala1160=
ENST00000445658.6:c.2742C>G	ENSP00000404047.2:p.Ala914=
ENST00000541774.5:c.3525C>G	ENSP00000446466.1:p.Ala1175=
ENST00000578373.5:c.*3360C>G	ENSP00000463427.1:n.*3360C>G
ENST00000584450.5:c.*149C>G	ENSP00000463714.1:n.*149C>G
ENST00000584601.5:c.3480C>G	ENSP00000462438.1:p.Ala1160=
NM_001005862.2:c.3480C>G , LRG_724t1:c.3480C>G	NP_001005862.1:p.Ala1160=
NM_001289936.1:c.3525C>G , LRG_724t4:c.3525C>G	NP_001276865.1:p.Ala1175=
NM_001289937.1:c.*149C>G	NP_001276866.1:n.*149C>G
NM_004448.3:c.3570C>G , LRG_724t2:c.3570C>G	NP_004439.2:p.Ala1190=
NR_110535.1:n.3894C>G
XM_024450641.1:c.3708C>G	XP_024306409.1:p.Ala1236=
XM_024450642.1:c.3663C>G	XP_024306410.1:p.Ala1221=
XM_024450643.1:c.3618C>G	XP_024306411.1:p.Ala1206=
NM_001005862.3:c.3480C>G	NP_001005862.1:p.Ala1160=
NM_001289936.2:c.3525C>G	NP_001276865.1:p.Ala1175=
NM_001289937.2:c.*149C>G	NP_001276866.1:n.*149C>G
NM_001382782.1:c.3480C>G	NP_001369711.1:p.Ala1160=
NM_001382783.1:c.3480C>G	NP_001369712.1:p.Ala1160=
NM_001382784.1:c.3687C>G	NP_001369713.1:p.Ala1229=
NM_001382785.1:c.3672C>G	NP_001369714.1:p.Ala1224=
NM_001382786.1:c.3651C>G	NP_001369715.1:p.Ala1217=
NM_001382787.1:c.3645C>G	NP_001369716.1:p.Ala1215=
NM_001382788.1:c.3600C>G	NP_001369717.1:p.Ala1200=
NM_001382789.1:c.3591C>G	NP_001369718.1:p.Ala1197=
NM_001382790.1:c.3567C>G	NP_001369719.1:p.Ala1189=
NM_001382791.1:c.3561C>G	NP_001369720.1:p.Ala1187=
NM_001382792.1:c.3534C>G	NP_001369721.1:p.Ala1178=
NM_001382793.1:c.3528C>G	NP_001369722.1:p.Ala1176=
NM_001382794.1:c.3528C>G	NP_001369723.1:p.Ala1176=
NM_001382795.1:c.3522C>G	NP_001369724.1:p.Ala1174=
NM_001382796.1:c.3483C>G	NP_001369725.1:p.Ala1161=
NM_001382797.1:c.3471C>G	NP_001369726.1:p.Ala1157=
NM_001382798.1:c.3414C>G	NP_001369727.1:p.Ala1138=
NM_001382799.1:c.3390C>G	NP_001369728.1:p.Ala1130=
NM_001382800.1:c.3384C>G	NP_001369729.1:p.Ala1128=
NM_001382801.1:c.3366C>G	NP_001369730.1:p.Ala1122=
NM_001382802.1:c.3312C>G	NP_001369731.1:p.Ala1104=
NM_001382803.1:c.*149C>G	NP_001369732.1:n.*149C>G
NM_001382804.1:c.2742C>G	NP_001369733.1:p.Ala914=
NM_001382805.1:c.2619C>G	NP_001369734.1:p.Ala873=
NM_001382806.1:c.2532C>G	NP_001369735.1:p.Ala844=
NM_004448.4:c.3570C>G MANE Select	NP_004439.2:p.Ala1190=
NR_110535.2:n.3808C>G