Canonical Allele Identifier: CA399314062

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884153C>G (hg19) ; chr17:g.39727900C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727900C>G , CM000679.2:g.39727900C>G	GRCh38
NC_000017.10:g.37884153C>G , CM000679.1:g.37884153C>G	GRCh37
NC_000017.9:g.35137679C>G	NCBI36
NG_007503.1:g.44761C>G , LRG_724:g.44761C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3624C>G MANE Select	ENSP00000269571.4:p.His1208Gln
ENST00000269571.9:c.3624C>G	ENSP00000269571.4:p.His1208Gln
ENST00000406381.6:c.3534C>G	ENSP00000385185.2:p.His1178Gln
ENST00000445658.6:c.2796C>G	ENSP00000404047.2:p.His932Gln
ENST00000541774.5:c.3579C>G	ENSP00000446466.1:p.His1193Gln
ENST00000578373.5:c.*3414C>G	ENSP00000463427.1:n.*3414C>G
ENST00000584450.5:c.*203C>G	ENSP00000463714.1:n.*203C>G
ENST00000584601.5:c.3534C>G	ENSP00000462438.1:p.His1178Gln
NM_001005862.2:c.3534C>G , LRG_724t1:c.3534C>G	NP_001005862.1:p.His1178Gln
NM_001289936.1:c.3579C>G , LRG_724t4:c.3579C>G	NP_001276865.1:p.His1193Gln
NM_001289937.1:c.*203C>G	NP_001276866.1:n.*203C>G
NM_004448.3:c.3624C>G , LRG_724t2:c.3624C>G	NP_004439.2:p.His1208Gln
NR_110535.1:n.3948C>G
XM_024450641.1:c.3762C>G	XP_024306409.1:p.His1254Gln
XM_024450642.1:c.3717C>G	XP_024306410.1:p.His1239Gln
XM_024450643.1:c.3672C>G	XP_024306411.1:p.His1224Gln
NM_001005862.3:c.3534C>G	NP_001005862.1:p.His1178Gln
NM_001289936.2:c.3579C>G	NP_001276865.1:p.His1193Gln
NM_001289937.2:c.*203C>G	NP_001276866.1:n.*203C>G
NM_001382782.1:c.3534C>G	NP_001369711.1:p.His1178Gln
NM_001382783.1:c.3534C>G	NP_001369712.1:p.His1178Gln
NM_001382784.1:c.3741C>G	NP_001369713.1:p.His1247Gln
NM_001382785.1:c.3726C>G	NP_001369714.1:p.His1242Gln
NM_001382786.1:c.3705C>G	NP_001369715.1:p.His1235Gln
NM_001382787.1:c.3699C>G	NP_001369716.1:p.His1233Gln
NM_001382788.1:c.3654C>G	NP_001369717.1:p.His1218Gln
NM_001382789.1:c.3645C>G	NP_001369718.1:p.His1215Gln
NM_001382790.1:c.3621C>G	NP_001369719.1:p.His1207Gln
NM_001382791.1:c.3615C>G	NP_001369720.1:p.His1205Gln
NM_001382792.1:c.3588C>G	NP_001369721.1:p.His1196Gln
NM_001382793.1:c.3582C>G	NP_001369722.1:p.His1194Gln
NM_001382794.1:c.3582C>G	NP_001369723.1:p.His1194Gln
NM_001382795.1:c.3576C>G	NP_001369724.1:p.His1192Gln
NM_001382796.1:c.3537C>G	NP_001369725.1:p.His1179Gln
NM_001382797.1:c.3525C>G	NP_001369726.1:p.His1175Gln
NM_001382798.1:c.3468C>G	NP_001369727.1:p.His1156Gln
NM_001382799.1:c.3444C>G	NP_001369728.1:p.His1148Gln
NM_001382800.1:c.3438C>G	NP_001369729.1:p.His1146Gln
NM_001382801.1:c.3420C>G	NP_001369730.1:p.His1140Gln
NM_001382802.1:c.3366C>G	NP_001369731.1:p.His1122Gln
NM_001382803.1:c.*203C>G	NP_001369732.1:n.*203C>G
NM_001382804.1:c.2796C>G	NP_001369733.1:p.His932Gln
NM_001382805.1:c.2673C>G	NP_001369734.1:p.His891Gln
NM_001382806.1:c.2586C>G	NP_001369735.1:p.His862Gln
NM_004448.4:c.3624C>G MANE Select	NP_004439.2:p.His1208Gln
NR_110535.2:n.3862C>G