Canonical Allele Identifier: CA399313985

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143308413
• MyVariant Identifiers: chr17:g.37884145C>G (hg19) ; chr17:g.39727892C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727892C>G , CM000679.2:g.39727892C>G	GRCh38
NC_000017.10:g.37884145C>G , CM000679.1:g.37884145C>G	GRCh37
NC_000017.9:g.35137671C>G	NCBI36
NG_007503.1:g.44753C>G , LRG_724:g.44753C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3616C>G MANE Select	ENSP00000269571.4:p.Gln1206Glu
ENST00000269571.9:c.3616C>G	ENSP00000269571.4:p.Gln1206Glu
ENST00000406381.6:c.3526C>G	ENSP00000385185.2:p.Gln1176Glu
ENST00000445658.6:c.2788C>G	ENSP00000404047.2:p.Gln930Glu
ENST00000541774.5:c.3571C>G	ENSP00000446466.1:p.Gln1191Glu
ENST00000578373.5:c.*3406C>G	ENSP00000463427.1:n.*3406C>G
ENST00000584450.5:c.*195C>G	ENSP00000463714.1:n.*195C>G
ENST00000584601.5:c.3526C>G	ENSP00000462438.1:p.Gln1176Glu
NM_001005862.2:c.3526C>G , LRG_724t1:c.3526C>G	NP_001005862.1:p.Gln1176Glu
NM_001289936.1:c.3571C>G , LRG_724t4:c.3571C>G	NP_001276865.1:p.Gln1191Glu
NM_001289937.1:c.*195C>G	NP_001276866.1:n.*195C>G
NM_004448.3:c.3616C>G , LRG_724t2:c.3616C>G	NP_004439.2:p.Gln1206Glu
NR_110535.1:n.3940C>G
XM_024450641.1:c.3754C>G	XP_024306409.1:p.Gln1252Glu
XM_024450642.1:c.3709C>G	XP_024306410.1:p.Gln1237Glu
XM_024450643.1:c.3664C>G	XP_024306411.1:p.Gln1222Glu
NM_001005862.3:c.3526C>G	NP_001005862.1:p.Gln1176Glu
NM_001289936.2:c.3571C>G	NP_001276865.1:p.Gln1191Glu
NM_001289937.2:c.*195C>G	NP_001276866.1:n.*195C>G
NM_001382782.1:c.3526C>G	NP_001369711.1:p.Gln1176Glu
NM_001382783.1:c.3526C>G	NP_001369712.1:p.Gln1176Glu
NM_001382784.1:c.3733C>G	NP_001369713.1:p.Gln1245Glu
NM_001382785.1:c.3718C>G	NP_001369714.1:p.Gln1240Glu
NM_001382786.1:c.3697C>G	NP_001369715.1:p.Gln1233Glu
NM_001382787.1:c.3691C>G	NP_001369716.1:p.Gln1231Glu
NM_001382788.1:c.3646C>G	NP_001369717.1:p.Gln1216Glu
NM_001382789.1:c.3637C>G	NP_001369718.1:p.Gln1213Glu
NM_001382790.1:c.3613C>G	NP_001369719.1:p.Gln1205Glu
NM_001382791.1:c.3607C>G	NP_001369720.1:p.Gln1203Glu
NM_001382792.1:c.3580C>G	NP_001369721.1:p.Gln1194Glu
NM_001382793.1:c.3574C>G	NP_001369722.1:p.Gln1192Glu
NM_001382794.1:c.3574C>G	NP_001369723.1:p.Gln1192Glu
NM_001382795.1:c.3568C>G	NP_001369724.1:p.Gln1190Glu
NM_001382796.1:c.3529C>G	NP_001369725.1:p.Gln1177Glu
NM_001382797.1:c.3517C>G	NP_001369726.1:p.Gln1173Glu
NM_001382798.1:c.3460C>G	NP_001369727.1:p.Gln1154Glu
NM_001382799.1:c.3436C>G	NP_001369728.1:p.Gln1146Glu
NM_001382800.1:c.3430C>G	NP_001369729.1:p.Gln1144Glu
NM_001382801.1:c.3412C>G	NP_001369730.1:p.Gln1138Glu
NM_001382802.1:c.3358C>G	NP_001369731.1:p.Gln1120Glu
NM_001382803.1:c.*195C>G	NP_001369732.1:n.*195C>G
NM_001382804.1:c.2788C>G	NP_001369733.1:p.Gln930Glu
NM_001382805.1:c.2665C>G	NP_001369734.1:p.Gln889Glu
NM_001382806.1:c.2578C>G	NP_001369735.1:p.Gln860Glu
NM_004448.4:c.3616C>G MANE Select	NP_004439.2:p.Gln1206Glu
NR_110535.2:n.3854C>G