Canonical Allele Identifier: CA399314531

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884212C>G (hg19) ; chr17:g.39727959C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727959C>G , CM000679.2:g.39727959C>G	GRCh38
NC_000017.10:g.37884212C>G , CM000679.1:g.37884212C>G	GRCh37
NC_000017.9:g.35137738C>G	NCBI36
NG_007503.1:g.44820C>G , LRG_724:g.44820C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3683C>G MANE Select	ENSP00000269571.4:p.Pro1228Arg
ENST00000269571.9:c.3683C>G	ENSP00000269571.4:p.Pro1228Arg
ENST00000406381.6:c.3593C>G	ENSP00000385185.2:p.Pro1198Arg
ENST00000445658.6:c.2855C>G	ENSP00000404047.2:p.Pro952Arg
ENST00000541774.5:c.3638C>G	ENSP00000446466.1:p.Pro1213Arg
ENST00000578373.5:c.*3473C>G	ENSP00000463427.1:n.*3473C>G
ENST00000584450.5:c.*262C>G	ENSP00000463714.1:n.*262C>G
ENST00000584601.5:c.3593C>G	ENSP00000462438.1:p.Pro1198Arg
NM_001005862.2:c.3593C>G , LRG_724t1:c.3593C>G	NP_001005862.1:p.Pro1198Arg
NM_001289936.1:c.3638C>G , LRG_724t4:c.3638C>G	NP_001276865.1:p.Pro1213Arg
NM_001289937.1:c.*262C>G	NP_001276866.1:n.*262C>G
NM_004448.3:c.3683C>G , LRG_724t2:c.3683C>G	NP_004439.2:p.Pro1228Arg
NR_110535.1:n.4007C>G
XM_024450641.1:c.3821C>G	XP_024306409.1:p.Pro1274Arg
XM_024450642.1:c.3776C>G	XP_024306410.1:p.Pro1259Arg
XM_024450643.1:c.3731C>G	XP_024306411.1:p.Pro1244Arg
NM_001005862.3:c.3593C>G	NP_001005862.1:p.Pro1198Arg
NM_001289936.2:c.3638C>G	NP_001276865.1:p.Pro1213Arg
NM_001289937.2:c.*262C>G	NP_001276866.1:n.*262C>G
NM_001382782.1:c.3593C>G	NP_001369711.1:p.Pro1198Arg
NM_001382783.1:c.3593C>G	NP_001369712.1:p.Pro1198Arg
NM_001382784.1:c.3800C>G	NP_001369713.1:p.Pro1267Arg
NM_001382785.1:c.3785C>G	NP_001369714.1:p.Pro1262Arg
NM_001382786.1:c.3764C>G	NP_001369715.1:p.Pro1255Arg
NM_001382787.1:c.3758C>G	NP_001369716.1:p.Pro1253Arg
NM_001382788.1:c.3713C>G	NP_001369717.1:p.Pro1238Arg
NM_001382789.1:c.3704C>G	NP_001369718.1:p.Pro1235Arg
NM_001382790.1:c.3680C>G	NP_001369719.1:p.Pro1227Arg
NM_001382791.1:c.3674C>G	NP_001369720.1:p.Pro1225Arg
NM_001382792.1:c.3647C>G	NP_001369721.1:p.Pro1216Arg
NM_001382793.1:c.3641C>G	NP_001369722.1:p.Pro1214Arg
NM_001382794.1:c.3641C>G	NP_001369723.1:p.Pro1214Arg
NM_001382795.1:c.3635C>G	NP_001369724.1:p.Pro1212Arg
NM_001382796.1:c.3596C>G	NP_001369725.1:p.Pro1199Arg
NM_001382797.1:c.3584C>G	NP_001369726.1:p.Pro1195Arg
NM_001382798.1:c.3527C>G	NP_001369727.1:p.Pro1176Arg
NM_001382799.1:c.3503C>G	NP_001369728.1:p.Pro1168Arg
NM_001382800.1:c.3497C>G	NP_001369729.1:p.Pro1166Arg
NM_001382801.1:c.3479C>G	NP_001369730.1:p.Pro1160Arg
NM_001382802.1:c.3425C>G	NP_001369731.1:p.Pro1142Arg
NM_001382803.1:c.*262C>G	NP_001369732.1:n.*262C>G
NM_001382804.1:c.2855C>G	NP_001369733.1:p.Pro952Arg
NM_001382805.1:c.2732C>G	NP_001369734.1:p.Pro911Arg
NM_001382806.1:c.2645C>G	NP_001369735.1:p.Pro882Arg
NM_004448.4:c.3683C>G MANE Select	NP_004439.2:p.Pro1228Arg
NR_110535.2:n.3921C>G