Canonical Allele Identifier: CA399310309

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143237686
• MyVariant Identifiers: chr17:g.37883602A>G (hg19) ; chr17:g.39727349A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727349A>G , CM000679.2:g.39727349A>G	GRCh38
NC_000017.10:g.37883602A>G , CM000679.1:g.37883602A>G	GRCh37
NC_000017.9:g.35137128A>G	NCBI36
NG_007503.1:g.44210A>G , LRG_724:g.44210A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3214A>G MANE Select	ENSP00000269571.4:p.Arg1072Gly
ENST00000269571.9:c.3214A>G	ENSP00000269571.4:p.Arg1072Gly
ENST00000406381.6:c.3124A>G	ENSP00000385185.2:p.Arg1042Gly
ENST00000445658.6:c.2386A>G	ENSP00000404047.2:p.Arg796Gly
ENST00000541774.5:c.3169A>G	ENSP00000446466.1:p.Arg1057Gly
ENST00000578373.5:c.*3004A>G	ENSP00000463427.1:n.*3004A>G
ENST00000584450.5:c.3160-340A>G	ENSP00000463714.1:n.3160-340A>G
ENST00000584601.5:c.3124A>G	ENSP00000462438.1:p.Arg1042Gly
NM_001005862.2:c.3124A>G , LRG_724t1:c.3124A>G	NP_001005862.1:p.Arg1042Gly
NM_001289936.1:c.3169A>G , LRG_724t4:c.3169A>G	NP_001276865.1:p.Arg1057Gly
NM_001289937.1:c.3160-340A>G	NP_001276866.1:n.3160-340A>G
NM_004448.3:c.3214A>G , LRG_724t2:c.3214A>G	NP_004439.2:p.Arg1072Gly
NR_110535.1:n.3538A>G
XM_024450641.1:c.3352A>G	XP_024306409.1:p.Arg1118Gly
XM_024450642.1:c.3307A>G	XP_024306410.1:p.Arg1103Gly
XM_024450643.1:c.3262A>G	XP_024306411.1:p.Arg1088Gly
NM_001005862.3:c.3124A>G	NP_001005862.1:p.Arg1042Gly
NM_001289936.2:c.3169A>G	NP_001276865.1:p.Arg1057Gly
NM_001289937.2:c.3160-340A>G	NP_001276866.1:n.3160-340A>G
NM_001382782.1:c.3124A>G	NP_001369711.1:p.Arg1042Gly
NM_001382783.1:c.3124A>G	NP_001369712.1:p.Arg1042Gly
NM_001382784.1:c.3331A>G	NP_001369713.1:p.Arg1111Gly
NM_001382785.1:c.3316A>G	NP_001369714.1:p.Arg1106Gly
NM_001382786.1:c.3295A>G	NP_001369715.1:p.Arg1099Gly
NM_001382787.1:c.3289A>G	NP_001369716.1:p.Arg1097Gly
NM_001382788.1:c.3244A>G	NP_001369717.1:p.Arg1082Gly
NM_001382789.1:c.3235A>G	NP_001369718.1:p.Arg1079Gly
NM_001382790.1:c.3211A>G	NP_001369719.1:p.Arg1071Gly
NM_001382791.1:c.3205A>G	NP_001369720.1:p.Arg1069Gly
NM_001382792.1:c.3178A>G	NP_001369721.1:p.Arg1060Gly
NM_001382793.1:c.3172A>G	NP_001369722.1:p.Arg1058Gly
NM_001382794.1:c.3172A>G	NP_001369723.1:p.Arg1058Gly
NM_001382795.1:c.3166A>G	NP_001369724.1:p.Arg1056Gly
NM_001382796.1:c.3127A>G	NP_001369725.1:p.Arg1043Gly
NM_001382797.1:c.3115A>G	NP_001369726.1:p.Arg1039Gly
NM_001382798.1:c.3058A>G	NP_001369727.1:p.Arg1020Gly
NM_001382799.1:c.3034A>G	NP_001369728.1:p.Arg1012Gly
NM_001382800.1:c.3028A>G	NP_001369729.1:p.Arg1010Gly
NM_001382801.1:c.3010A>G	NP_001369730.1:p.Arg1004Gly
NM_001382802.1:c.2956A>G	NP_001369731.1:p.Arg986Gly
NM_001382803.1:c.3118-340A>G	NP_001369732.1:n.3118-340A>G
NM_001382804.1:c.2386A>G	NP_001369733.1:p.Arg796Gly
NM_001382805.1:c.2263A>G	NP_001369734.1:p.Arg755Gly
NM_001382806.1:c.2176A>G	NP_001369735.1:p.Arg726Gly
NM_004448.4:c.3214A>G MANE Select	NP_004439.2:p.Arg1072Gly
NR_110535.2:n.3452A>G