Canonical Allele Identifier: CA399312876

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143289047
• MyVariant Identifiers: chr17:g.37883969C>G (hg19) ; chr17:g.39727716C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727716C>G , CM000679.2:g.39727716C>G	GRCh38
NC_000017.10:g.37883969C>G , CM000679.1:g.37883969C>G	GRCh37
NC_000017.9:g.35137495C>G	NCBI36
NG_007503.1:g.44577C>G , LRG_724:g.44577C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3440C>G MANE Select	ENSP00000269571.4:p.Pro1147Arg
ENST00000269571.9:c.3440C>G	ENSP00000269571.4:p.Pro1147Arg
ENST00000406381.6:c.3350C>G	ENSP00000385185.2:p.Pro1117Arg
ENST00000445658.6:c.2612C>G	ENSP00000404047.2:p.Pro871Arg
ENST00000541774.5:c.3395C>G	ENSP00000446466.1:p.Pro1132Arg
ENST00000578373.5:c.*3230C>G	ENSP00000463427.1:n.*3230C>G
ENST00000584450.5:c.*19C>G	ENSP00000463714.1:n.*19C>G
ENST00000584601.5:c.3350C>G	ENSP00000462438.1:p.Pro1117Arg
NM_001005862.2:c.3350C>G , LRG_724t1:c.3350C>G	NP_001005862.1:p.Pro1117Arg
NM_001289936.1:c.3395C>G , LRG_724t4:c.3395C>G	NP_001276865.1:p.Pro1132Arg
NM_001289937.1:c.*19C>G	NP_001276866.1:n.*19C>G
NM_004448.3:c.3440C>G , LRG_724t2:c.3440C>G	NP_004439.2:p.Pro1147Arg
NR_110535.1:n.3764C>G
XM_024450641.1:c.3578C>G	XP_024306409.1:p.Pro1193Arg
XM_024450642.1:c.3533C>G	XP_024306410.1:p.Pro1178Arg
XM_024450643.1:c.3488C>G	XP_024306411.1:p.Pro1163Arg
NM_001005862.3:c.3350C>G	NP_001005862.1:p.Pro1117Arg
NM_001289936.2:c.3395C>G	NP_001276865.1:p.Pro1132Arg
NM_001289937.2:c.*19C>G	NP_001276866.1:n.*19C>G
NM_001382782.1:c.3350C>G	NP_001369711.1:p.Pro1117Arg
NM_001382783.1:c.3350C>G	NP_001369712.1:p.Pro1117Arg
NM_001382784.1:c.3557C>G	NP_001369713.1:p.Pro1186Arg
NM_001382785.1:c.3542C>G	NP_001369714.1:p.Pro1181Arg
NM_001382786.1:c.3521C>G	NP_001369715.1:p.Pro1174Arg
NM_001382787.1:c.3515C>G	NP_001369716.1:p.Pro1172Arg
NM_001382788.1:c.3470C>G	NP_001369717.1:p.Pro1157Arg
NM_001382789.1:c.3461C>G	NP_001369718.1:p.Pro1154Arg
NM_001382790.1:c.3437C>G	NP_001369719.1:p.Pro1146Arg
NM_001382791.1:c.3431C>G	NP_001369720.1:p.Pro1144Arg
NM_001382792.1:c.3404C>G	NP_001369721.1:p.Pro1135Arg
NM_001382793.1:c.3398C>G	NP_001369722.1:p.Pro1133Arg
NM_001382794.1:c.3398C>G	NP_001369723.1:p.Pro1133Arg
NM_001382795.1:c.3392C>G	NP_001369724.1:p.Pro1131Arg
NM_001382796.1:c.3353C>G	NP_001369725.1:p.Pro1118Arg
NM_001382797.1:c.3341C>G	NP_001369726.1:p.Pro1114Arg
NM_001382798.1:c.3284C>G	NP_001369727.1:p.Pro1095Arg
NM_001382799.1:c.3260C>G	NP_001369728.1:p.Pro1087Arg
NM_001382800.1:c.3254C>G	NP_001369729.1:p.Pro1085Arg
NM_001382801.1:c.3236C>G	NP_001369730.1:p.Pro1079Arg
NM_001382802.1:c.3182C>G	NP_001369731.1:p.Pro1061Arg
NM_001382803.1:c.*19C>G	NP_001369732.1:n.*19C>G
NM_001382804.1:c.2612C>G	NP_001369733.1:p.Pro871Arg
NM_001382805.1:c.2489C>G	NP_001369734.1:p.Pro830Arg
NM_001382806.1:c.2402C>G	NP_001369735.1:p.Pro801Arg
NM_004448.4:c.3440C>G MANE Select	NP_004439.2:p.Pro1147Arg
NR_110535.2:n.3678C>G