Canonical Allele Identifier: CA399314515

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884209C>G (hg19) ; chr17:g.39727956C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727956C>G , CM000679.2:g.39727956C>G	GRCh38
NC_000017.10:g.37884209C>G , CM000679.1:g.37884209C>G	GRCh37
NC_000017.9:g.35137735C>G	NCBI36
NG_007503.1:g.44817C>G , LRG_724:g.44817C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3680C>G MANE Select	ENSP00000269571.4:p.Pro1227Arg
ENST00000269571.9:c.3680C>G	ENSP00000269571.4:p.Pro1227Arg
ENST00000406381.6:c.3590C>G	ENSP00000385185.2:p.Pro1197Arg
ENST00000445658.6:c.2852C>G	ENSP00000404047.2:p.Pro951Arg
ENST00000541774.5:c.3635C>G	ENSP00000446466.1:p.Pro1212Arg
ENST00000578373.5:c.*3470C>G	ENSP00000463427.1:n.*3470C>G
ENST00000584450.5:c.*259C>G	ENSP00000463714.1:n.*259C>G
ENST00000584601.5:c.3590C>G	ENSP00000462438.1:p.Pro1197Arg
NM_001005862.2:c.3590C>G , LRG_724t1:c.3590C>G	NP_001005862.1:p.Pro1197Arg
NM_001289936.1:c.3635C>G , LRG_724t4:c.3635C>G	NP_001276865.1:p.Pro1212Arg
NM_001289937.1:c.*259C>G	NP_001276866.1:n.*259C>G
NM_004448.3:c.3680C>G , LRG_724t2:c.3680C>G	NP_004439.2:p.Pro1227Arg
NR_110535.1:n.4004C>G
XM_024450641.1:c.3818C>G	XP_024306409.1:p.Pro1273Arg
XM_024450642.1:c.3773C>G	XP_024306410.1:p.Pro1258Arg
XM_024450643.1:c.3728C>G	XP_024306411.1:p.Pro1243Arg
NM_001005862.3:c.3590C>G	NP_001005862.1:p.Pro1197Arg
NM_001289936.2:c.3635C>G	NP_001276865.1:p.Pro1212Arg
NM_001289937.2:c.*259C>G	NP_001276866.1:n.*259C>G
NM_001382782.1:c.3590C>G	NP_001369711.1:p.Pro1197Arg
NM_001382783.1:c.3590C>G	NP_001369712.1:p.Pro1197Arg
NM_001382784.1:c.3797C>G	NP_001369713.1:p.Pro1266Arg
NM_001382785.1:c.3782C>G	NP_001369714.1:p.Pro1261Arg
NM_001382786.1:c.3761C>G	NP_001369715.1:p.Pro1254Arg
NM_001382787.1:c.3755C>G	NP_001369716.1:p.Pro1252Arg
NM_001382788.1:c.3710C>G	NP_001369717.1:p.Pro1237Arg
NM_001382789.1:c.3701C>G	NP_001369718.1:p.Pro1234Arg
NM_001382790.1:c.3677C>G	NP_001369719.1:p.Pro1226Arg
NM_001382791.1:c.3671C>G	NP_001369720.1:p.Pro1224Arg
NM_001382792.1:c.3644C>G	NP_001369721.1:p.Pro1215Arg
NM_001382793.1:c.3638C>G	NP_001369722.1:p.Pro1213Arg
NM_001382794.1:c.3638C>G	NP_001369723.1:p.Pro1213Arg
NM_001382795.1:c.3632C>G	NP_001369724.1:p.Pro1211Arg
NM_001382796.1:c.3593C>G	NP_001369725.1:p.Pro1198Arg
NM_001382797.1:c.3581C>G	NP_001369726.1:p.Pro1194Arg
NM_001382798.1:c.3524C>G	NP_001369727.1:p.Pro1175Arg
NM_001382799.1:c.3500C>G	NP_001369728.1:p.Pro1167Arg
NM_001382800.1:c.3494C>G	NP_001369729.1:p.Pro1165Arg
NM_001382801.1:c.3476C>G	NP_001369730.1:p.Pro1159Arg
NM_001382802.1:c.3422C>G	NP_001369731.1:p.Pro1141Arg
NM_001382803.1:c.*259C>G	NP_001369732.1:n.*259C>G
NM_001382804.1:c.2852C>G	NP_001369733.1:p.Pro951Arg
NM_001382805.1:c.2729C>G	NP_001369734.1:p.Pro910Arg
NM_001382806.1:c.2642C>G	NP_001369735.1:p.Pro881Arg
NM_004448.4:c.3680C>G MANE Select	NP_004439.2:p.Pro1227Arg
NR_110535.2:n.3918C>G