Canonical Allele Identifier: CA399313032

Gene: ERBB2

Linked Data

• dbSNP Id: rs1210088528
• MyVariant Identifiers: chr17:g.37884010C>G (hg19) ; chr17:g.39727757C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727757C>G , CM000679.2:g.39727757C>G	GRCh38
NC_000017.10:g.37884010C>G , CM000679.1:g.37884010C>G	GRCh37
NC_000017.9:g.35137536C>G	NCBI36
NG_007503.1:g.44618C>G , LRG_724:g.44618C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3481C>G MANE Select	ENSP00000269571.4:p.Arg1161Gly
ENST00000269571.9:c.3481C>G	ENSP00000269571.4:p.Arg1161Gly
ENST00000406381.6:c.3391C>G	ENSP00000385185.2:p.Arg1131Gly
ENST00000445658.6:c.2653C>G	ENSP00000404047.2:p.Arg885Gly
ENST00000541774.5:c.3436C>G	ENSP00000446466.1:p.Arg1146Gly
ENST00000578373.5:c.*3271C>G	ENSP00000463427.1:n.*3271C>G
ENST00000584450.5:c.*60C>G	ENSP00000463714.1:n.*60C>G
ENST00000584601.5:c.3391C>G	ENSP00000462438.1:p.Arg1131Gly
NM_001005862.2:c.3391C>G , LRG_724t1:c.3391C>G	NP_001005862.1:p.Arg1131Gly
NM_001289936.1:c.3436C>G , LRG_724t4:c.3436C>G	NP_001276865.1:p.Arg1146Gly
NM_001289937.1:c.*60C>G	NP_001276866.1:n.*60C>G
NM_004448.3:c.3481C>G , LRG_724t2:c.3481C>G	NP_004439.2:p.Arg1161Gly
NR_110535.1:n.3805C>G
XM_024450641.1:c.3619C>G	XP_024306409.1:p.Arg1207Gly
XM_024450642.1:c.3574C>G	XP_024306410.1:p.Arg1192Gly
XM_024450643.1:c.3529C>G	XP_024306411.1:p.Arg1177Gly
NM_001005862.3:c.3391C>G	NP_001005862.1:p.Arg1131Gly
NM_001289936.2:c.3436C>G	NP_001276865.1:p.Arg1146Gly
NM_001289937.2:c.*60C>G	NP_001276866.1:n.*60C>G
NM_001382782.1:c.3391C>G	NP_001369711.1:p.Arg1131Gly
NM_001382783.1:c.3391C>G	NP_001369712.1:p.Arg1131Gly
NM_001382784.1:c.3598C>G	NP_001369713.1:p.Arg1200Gly
NM_001382785.1:c.3583C>G	NP_001369714.1:p.Arg1195Gly
NM_001382786.1:c.3562C>G	NP_001369715.1:p.Arg1188Gly
NM_001382787.1:c.3556C>G	NP_001369716.1:p.Arg1186Gly
NM_001382788.1:c.3511C>G	NP_001369717.1:p.Arg1171Gly
NM_001382789.1:c.3502C>G	NP_001369718.1:p.Arg1168Gly
NM_001382790.1:c.3478C>G	NP_001369719.1:p.Arg1160Gly
NM_001382791.1:c.3472C>G	NP_001369720.1:p.Arg1158Gly
NM_001382792.1:c.3445C>G	NP_001369721.1:p.Arg1149Gly
NM_001382793.1:c.3439C>G	NP_001369722.1:p.Arg1147Gly
NM_001382794.1:c.3439C>G	NP_001369723.1:p.Arg1147Gly
NM_001382795.1:c.3433C>G	NP_001369724.1:p.Arg1145Gly
NM_001382796.1:c.3394C>G	NP_001369725.1:p.Arg1132Gly
NM_001382797.1:c.3382C>G	NP_001369726.1:p.Arg1128Gly
NM_001382798.1:c.3325C>G	NP_001369727.1:p.Arg1109Gly
NM_001382799.1:c.3301C>G	NP_001369728.1:p.Arg1101Gly
NM_001382800.1:c.3295C>G	NP_001369729.1:p.Arg1099Gly
NM_001382801.1:c.3277C>G	NP_001369730.1:p.Arg1093Gly
NM_001382802.1:c.3223C>G	NP_001369731.1:p.Arg1075Gly
NM_001382803.1:c.*60C>G	NP_001369732.1:n.*60C>G
NM_001382804.1:c.2653C>G	NP_001369733.1:p.Arg885Gly
NM_001382805.1:c.2530C>G	NP_001369734.1:p.Arg844Gly
NM_001382806.1:c.2443C>G	NP_001369735.1:p.Arg815Gly
NM_004448.4:c.3481C>G MANE Select	NP_004439.2:p.Arg1161Gly
NR_110535.2:n.3719C>G