Canonical Allele Identifier: CA399312576

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143252770
• MyVariant Identifiers: chr17:g.37883727T>G (hg19) ; chr17:g.39727474T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727474T>G , CM000679.2:g.39727474T>G	GRCh38
NC_000017.10:g.37883727T>G , CM000679.1:g.37883727T>G	GRCh37
NC_000017.9:g.35137253T>G	NCBI36
NG_007503.1:g.44335T>G , LRG_724:g.44335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3339T>G MANE Select	ENSP00000269571.4:p.Ser1113Arg
ENST00000269571.9:c.3339T>G	ENSP00000269571.4:p.Ser1113Arg
ENST00000406381.6:c.3249T>G	ENSP00000385185.2:p.Ser1083Arg
ENST00000445658.6:c.2511T>G	ENSP00000404047.2:p.Ser837Arg
ENST00000541774.5:c.3294T>G	ENSP00000446466.1:p.Ser1098Arg
ENST00000578373.5:c.*3129T>G	ENSP00000463427.1:n.*3129T>G
ENST00000584450.5:c.3160-215T>G	ENSP00000463714.1:n.3160-215T>G
ENST00000584601.5:c.3249T>G	ENSP00000462438.1:p.Ser1083Arg
NM_001005862.2:c.3249T>G , LRG_724t1:c.3249T>G	NP_001005862.1:p.Ser1083Arg
NM_001289936.1:c.3294T>G , LRG_724t4:c.3294T>G	NP_001276865.1:p.Ser1098Arg
NM_001289937.1:c.3160-215T>G	NP_001276866.1:n.3160-215T>G
NM_004448.3:c.3339T>G , LRG_724t2:c.3339T>G	NP_004439.2:p.Ser1113Arg
NR_110535.1:n.3663T>G
XM_024450641.1:c.3477T>G	XP_024306409.1:p.Ser1159Arg
XM_024450642.1:c.3432T>G	XP_024306410.1:p.Ser1144Arg
XM_024450643.1:c.3387T>G	XP_024306411.1:p.Ser1129Arg
NM_001005862.3:c.3249T>G	NP_001005862.1:p.Ser1083Arg
NM_001289936.2:c.3294T>G	NP_001276865.1:p.Ser1098Arg
NM_001289937.2:c.3160-215T>G	NP_001276866.1:n.3160-215T>G
NM_001382782.1:c.3249T>G	NP_001369711.1:p.Ser1083Arg
NM_001382783.1:c.3249T>G	NP_001369712.1:p.Ser1083Arg
NM_001382784.1:c.3456T>G	NP_001369713.1:p.Ser1152Arg
NM_001382785.1:c.3441T>G	NP_001369714.1:p.Ser1147Arg
NM_001382786.1:c.3420T>G	NP_001369715.1:p.Ser1140Arg
NM_001382787.1:c.3414T>G	NP_001369716.1:p.Ser1138Arg
NM_001382788.1:c.3369T>G	NP_001369717.1:p.Ser1123Arg
NM_001382789.1:c.3360T>G	NP_001369718.1:p.Ser1120Arg
NM_001382790.1:c.3336T>G	NP_001369719.1:p.Ser1112Arg
NM_001382791.1:c.3330T>G	NP_001369720.1:p.Ser1110Arg
NM_001382792.1:c.3303T>G	NP_001369721.1:p.Ser1101Arg
NM_001382793.1:c.3297T>G	NP_001369722.1:p.Ser1099Arg
NM_001382794.1:c.3297T>G	NP_001369723.1:p.Ser1099Arg
NM_001382795.1:c.3291T>G	NP_001369724.1:p.Ser1097Arg
NM_001382796.1:c.3252T>G	NP_001369725.1:p.Ser1084Arg
NM_001382797.1:c.3240T>G	NP_001369726.1:p.Ser1080Arg
NM_001382798.1:c.3183T>G	NP_001369727.1:p.Ser1061Arg
NM_001382799.1:c.3159T>G	NP_001369728.1:p.Ser1053Arg
NM_001382800.1:c.3153T>G	NP_001369729.1:p.Ser1051Arg
NM_001382801.1:c.3135T>G	NP_001369730.1:p.Ser1045Arg
NM_001382802.1:c.3081T>G	NP_001369731.1:p.Ser1027Arg
NM_001382803.1:c.3118-215T>G	NP_001369732.1:n.3118-215T>G
NM_001382804.1:c.2511T>G	NP_001369733.1:p.Ser837Arg
NM_001382805.1:c.2388T>G	NP_001369734.1:p.Ser796Arg
NM_001382806.1:c.2301T>G	NP_001369735.1:p.Ser767Arg
NM_004448.4:c.3339T>G MANE Select	NP_004439.2:p.Ser1113Arg
NR_110535.2:n.3577T>G