Canonical Allele Identifier: CA399313874

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884128A>G (hg19) ; chr17:g.39727875A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727875A>G , CM000679.2:g.39727875A>G	GRCh38
NC_000017.10:g.37884128A>G , CM000679.1:g.37884128A>G	GRCh37
NC_000017.9:g.35137654A>G	NCBI36
NG_007503.1:g.44736A>G , LRG_724:g.44736A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3599A>G MANE Select	ENSP00000269571.4:p.Gln1200Arg
ENST00000269571.9:c.3599A>G	ENSP00000269571.4:p.Gln1200Arg
ENST00000406381.6:c.3509A>G	ENSP00000385185.2:p.Gln1170Arg
ENST00000445658.6:c.2771A>G	ENSP00000404047.2:p.Gln924Arg
ENST00000541774.5:c.3554A>G	ENSP00000446466.1:p.Gln1185Arg
ENST00000578373.5:c.*3389A>G	ENSP00000463427.1:n.*3389A>G
ENST00000584450.5:c.*178A>G	ENSP00000463714.1:n.*178A>G
ENST00000584601.5:c.3509A>G	ENSP00000462438.1:p.Gln1170Arg
NM_001005862.2:c.3509A>G , LRG_724t1:c.3509A>G	NP_001005862.1:p.Gln1170Arg
NM_001289936.1:c.3554A>G , LRG_724t4:c.3554A>G	NP_001276865.1:p.Gln1185Arg
NM_001289937.1:c.*178A>G	NP_001276866.1:n.*178A>G
NM_004448.3:c.3599A>G , LRG_724t2:c.3599A>G	NP_004439.2:p.Gln1200Arg
NR_110535.1:n.3923A>G
XM_024450641.1:c.3737A>G	XP_024306409.1:p.Gln1246Arg
XM_024450642.1:c.3692A>G	XP_024306410.1:p.Gln1231Arg
XM_024450643.1:c.3647A>G	XP_024306411.1:p.Gln1216Arg
NM_001005862.3:c.3509A>G	NP_001005862.1:p.Gln1170Arg
NM_001289936.2:c.3554A>G	NP_001276865.1:p.Gln1185Arg
NM_001289937.2:c.*178A>G	NP_001276866.1:n.*178A>G
NM_001382782.1:c.3509A>G	NP_001369711.1:p.Gln1170Arg
NM_001382783.1:c.3509A>G	NP_001369712.1:p.Gln1170Arg
NM_001382784.1:c.3716A>G	NP_001369713.1:p.Gln1239Arg
NM_001382785.1:c.3701A>G	NP_001369714.1:p.Gln1234Arg
NM_001382786.1:c.3680A>G	NP_001369715.1:p.Gln1227Arg
NM_001382787.1:c.3674A>G	NP_001369716.1:p.Gln1225Arg
NM_001382788.1:c.3629A>G	NP_001369717.1:p.Gln1210Arg
NM_001382789.1:c.3620A>G	NP_001369718.1:p.Gln1207Arg
NM_001382790.1:c.3596A>G	NP_001369719.1:p.Gln1199Arg
NM_001382791.1:c.3590A>G	NP_001369720.1:p.Gln1197Arg
NM_001382792.1:c.3563A>G	NP_001369721.1:p.Gln1188Arg
NM_001382793.1:c.3557A>G	NP_001369722.1:p.Gln1186Arg
NM_001382794.1:c.3557A>G	NP_001369723.1:p.Gln1186Arg
NM_001382795.1:c.3551A>G	NP_001369724.1:p.Gln1184Arg
NM_001382796.1:c.3512A>G	NP_001369725.1:p.Gln1171Arg
NM_001382797.1:c.3500A>G	NP_001369726.1:p.Gln1167Arg
NM_001382798.1:c.3443A>G	NP_001369727.1:p.Gln1148Arg
NM_001382799.1:c.3419A>G	NP_001369728.1:p.Gln1140Arg
NM_001382800.1:c.3413A>G	NP_001369729.1:p.Gln1138Arg
NM_001382801.1:c.3395A>G	NP_001369730.1:p.Gln1132Arg
NM_001382802.1:c.3341A>G	NP_001369731.1:p.Gln1114Arg
NM_001382803.1:c.*178A>G	NP_001369732.1:n.*178A>G
NM_001382804.1:c.2771A>G	NP_001369733.1:p.Gln924Arg
NM_001382805.1:c.2648A>G	NP_001369734.1:p.Gln883Arg
NM_001382806.1:c.2561A>G	NP_001369735.1:p.Gln854Arg
NM_004448.4:c.3599A>G MANE Select	NP_004439.2:p.Gln1200Arg
NR_110535.2:n.3837A>G