Canonical Allele Identifier: CA399310627

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143243841
• MyVariant Identifiers: chr17:g.37883653G>C (hg19) ; chr17:g.39727400G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727400G>C , CM000679.2:g.39727400G>C	GRCh38
NC_000017.10:g.37883653G>C , CM000679.1:g.37883653G>C	GRCh37
NC_000017.9:g.35137179G>C	NCBI36
NG_007503.1:g.44261G>C , LRG_724:g.44261G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3265G>C MANE Select	ENSP00000269571.4:p.Asp1089His
ENST00000269571.9:c.3265G>C	ENSP00000269571.4:p.Asp1089His
ENST00000406381.6:c.3175G>C	ENSP00000385185.2:p.Asp1059His
ENST00000445658.6:c.2437G>C	ENSP00000404047.2:p.Asp813His
ENST00000541774.5:c.3220G>C	ENSP00000446466.1:p.Asp1074His
ENST00000578373.5:c.*3055G>C	ENSP00000463427.1:n.*3055G>C
ENST00000584450.5:c.3160-289G>C	ENSP00000463714.1:n.3160-289G>C
ENST00000584601.5:c.3175G>C	ENSP00000462438.1:p.Asp1059His
NM_001005862.2:c.3175G>C , LRG_724t1:c.3175G>C	NP_001005862.1:p.Asp1059His
NM_001289936.1:c.3220G>C , LRG_724t4:c.3220G>C	NP_001276865.1:p.Asp1074His
NM_001289937.1:c.3160-289G>C	NP_001276866.1:n.3160-289G>C
NM_004448.3:c.3265G>C , LRG_724t2:c.3265G>C	NP_004439.2:p.Asp1089His
NR_110535.1:n.3589G>C
XM_024450641.1:c.3403G>C	XP_024306409.1:p.Asp1135His
XM_024450642.1:c.3358G>C	XP_024306410.1:p.Asp1120His
XM_024450643.1:c.3313G>C	XP_024306411.1:p.Asp1105His
NM_001005862.3:c.3175G>C	NP_001005862.1:p.Asp1059His
NM_001289936.2:c.3220G>C	NP_001276865.1:p.Asp1074His
NM_001289937.2:c.3160-289G>C	NP_001276866.1:n.3160-289G>C
NM_001382782.1:c.3175G>C	NP_001369711.1:p.Asp1059His
NM_001382783.1:c.3175G>C	NP_001369712.1:p.Asp1059His
NM_001382784.1:c.3382G>C	NP_001369713.1:p.Asp1128His
NM_001382785.1:c.3367G>C	NP_001369714.1:p.Asp1123His
NM_001382786.1:c.3346G>C	NP_001369715.1:p.Asp1116His
NM_001382787.1:c.3340G>C	NP_001369716.1:p.Asp1114His
NM_001382788.1:c.3295G>C	NP_001369717.1:p.Asp1099His
NM_001382789.1:c.3286G>C	NP_001369718.1:p.Asp1096His
NM_001382790.1:c.3262G>C	NP_001369719.1:p.Asp1088His
NM_001382791.1:c.3256G>C	NP_001369720.1:p.Asp1086His
NM_001382792.1:c.3229G>C	NP_001369721.1:p.Asp1077His
NM_001382793.1:c.3223G>C	NP_001369722.1:p.Asp1075His
NM_001382794.1:c.3223G>C	NP_001369723.1:p.Asp1075His
NM_001382795.1:c.3217G>C	NP_001369724.1:p.Asp1073His
NM_001382796.1:c.3178G>C	NP_001369725.1:p.Asp1060His
NM_001382797.1:c.3166G>C	NP_001369726.1:p.Asp1056His
NM_001382798.1:c.3109G>C	NP_001369727.1:p.Asp1037His
NM_001382799.1:c.3085G>C	NP_001369728.1:p.Asp1029His
NM_001382800.1:c.3079G>C	NP_001369729.1:p.Asp1027His
NM_001382801.1:c.3061G>C	NP_001369730.1:p.Asp1021His
NM_001382802.1:c.3007G>C	NP_001369731.1:p.Asp1003His
NM_001382803.1:c.3118-289G>C	NP_001369732.1:n.3118-289G>C
NM_001382804.1:c.2437G>C	NP_001369733.1:p.Asp813His
NM_001382805.1:c.2314G>C	NP_001369734.1:p.Asp772His
NM_001382806.1:c.2227G>C	NP_001369735.1:p.Asp743His
NM_004448.4:c.3265G>C MANE Select	NP_004439.2:p.Asp1089His
NR_110535.2:n.3503G>C