Canonical Allele Identifier: CA499671609

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883602A>C (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3214A>C MANE Select	ENSP00000269571.4:p.Arg1072=
ENST00000269571.9:c.3214A>C	ENSP00000269571.4:p.Arg1072=
ENST00000406381.6:c.3124A>C	ENSP00000385185.2:p.Arg1042=
ENST00000445658.6:c.2386A>C	ENSP00000404047.2:p.Arg796=
ENST00000541774.5:c.3169A>C	ENSP00000446466.1:p.Arg1057=
ENST00000578373.5:c.*3004A>C	ENSP00000463427.1:n.*3004A>C
ENST00000584450.5:c.3160-340A>C	ENSP00000463714.1:n.3160-340A>C
ENST00000584601.5:c.3124A>C	ENSP00000462438.1:p.Arg1042=
NM_001005862.2:c.3124A>C , LRG_724t1:c.3124A>C	NP_001005862.1:p.Arg1042=
NM_001289936.1:c.3169A>C , LRG_724t4:c.3169A>C	NP_001276865.1:p.Arg1057=
NM_001289937.1:c.3160-340A>C	NP_001276866.1:n.3160-340A>C
NM_004448.3:c.3214A>C , LRG_724t2:c.3214A>C	NP_004439.2:p.Arg1072=
NR_110535.1:n.3538A>C
XM_024450641.1:c.3352A>C	XP_024306409.1:p.Arg1118=
XM_024450642.1:c.3307A>C	XP_024306410.1:p.Arg1103=
XM_024450643.1:c.3262A>C	XP_024306411.1:p.Arg1088=
NM_001005862.3:c.3124A>C	NP_001005862.1:p.Arg1042=
NM_001289936.2:c.3169A>C	NP_001276865.1:p.Arg1057=
NM_001289937.2:c.3160-340A>C	NP_001276866.1:n.3160-340A>C
NM_001382782.1:c.3124A>C	NP_001369711.1:p.Arg1042=
NM_001382783.1:c.3124A>C	NP_001369712.1:p.Arg1042=
NM_001382784.1:c.3331A>C	NP_001369713.1:p.Arg1111=
NM_001382785.1:c.3316A>C	NP_001369714.1:p.Arg1106=
NM_001382786.1:c.3295A>C	NP_001369715.1:p.Arg1099=
NM_001382787.1:c.3289A>C	NP_001369716.1:p.Arg1097=
NM_001382788.1:c.3244A>C	NP_001369717.1:p.Arg1082=
NM_001382789.1:c.3235A>C	NP_001369718.1:p.Arg1079=
NM_001382790.1:c.3211A>C	NP_001369719.1:p.Arg1071=
NM_001382791.1:c.3205A>C	NP_001369720.1:p.Arg1069=
NM_001382792.1:c.3178A>C	NP_001369721.1:p.Arg1060=
NM_001382793.1:c.3172A>C	NP_001369722.1:p.Arg1058=
NM_001382794.1:c.3172A>C	NP_001369723.1:p.Arg1058=
NM_001382795.1:c.3166A>C	NP_001369724.1:p.Arg1056=
NM_001382796.1:c.3127A>C	NP_001369725.1:p.Arg1043=
NM_001382797.1:c.3115A>C	NP_001369726.1:p.Arg1039=
NM_001382798.1:c.3058A>C	NP_001369727.1:p.Arg1020=
NM_001382799.1:c.3034A>C	NP_001369728.1:p.Arg1012=
NM_001382800.1:c.3028A>C	NP_001369729.1:p.Arg1010=
NM_001382801.1:c.3010A>C	NP_001369730.1:p.Arg1004=
NM_001382802.1:c.2956A>C	NP_001369731.1:p.Arg986=
NM_001382803.1:c.3118-340A>C	NP_001369732.1:n.3118-340A>C
NM_001382804.1:c.2386A>C	NP_001369733.1:p.Arg796=
NM_001382805.1:c.2263A>C	NP_001369734.1:p.Arg755=
NM_001382806.1:c.2176A>C	NP_001369735.1:p.Arg726=
NM_004448.4:c.3214A>C MANE Select	NP_004439.2:p.Arg1072=
NR_110535.2:n.3452A>C