Canonical Allele Identifier: CA399313478

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143300839
• MyVariant Identifiers: chr17:g.37884076G>C (hg19) ; chr17:g.39727823G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727823G>C , CM000679.2:g.39727823G>C	GRCh38
NC_000017.10:g.37884076G>C , CM000679.1:g.37884076G>C	GRCh37
NC_000017.9:g.35137602G>C	NCBI36
NG_007503.1:g.44684G>C , LRG_724:g.44684G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3547G>C MANE Select	ENSP00000269571.4:p.Asp1183His
ENST00000269571.9:c.3547G>C	ENSP00000269571.4:p.Asp1183His
ENST00000406381.6:c.3457G>C	ENSP00000385185.2:p.Asp1153His
ENST00000445658.6:c.2719G>C	ENSP00000404047.2:p.Asp907His
ENST00000541774.5:c.3502G>C	ENSP00000446466.1:p.Asp1168His
ENST00000578373.5:c.*3337G>C	ENSP00000463427.1:n.*3337G>C
ENST00000584450.5:c.*126G>C	ENSP00000463714.1:n.*126G>C
ENST00000584601.5:c.3457G>C	ENSP00000462438.1:p.Asp1153His
NM_001005862.2:c.3457G>C , LRG_724t1:c.3457G>C	NP_001005862.1:p.Asp1153His
NM_001289936.1:c.3502G>C , LRG_724t4:c.3502G>C	NP_001276865.1:p.Asp1168His
NM_001289937.1:c.*126G>C	NP_001276866.1:n.*126G>C
NM_004448.3:c.3547G>C , LRG_724t2:c.3547G>C	NP_004439.2:p.Asp1183His
NR_110535.1:n.3871G>C
XM_024450641.1:c.3685G>C	XP_024306409.1:p.Asp1229His
XM_024450642.1:c.3640G>C	XP_024306410.1:p.Asp1214His
XM_024450643.1:c.3595G>C	XP_024306411.1:p.Asp1199His
NM_001005862.3:c.3457G>C	NP_001005862.1:p.Asp1153His
NM_001289936.2:c.3502G>C	NP_001276865.1:p.Asp1168His
NM_001289937.2:c.*126G>C	NP_001276866.1:n.*126G>C
NM_001382782.1:c.3457G>C	NP_001369711.1:p.Asp1153His
NM_001382783.1:c.3457G>C	NP_001369712.1:p.Asp1153His
NM_001382784.1:c.3664G>C	NP_001369713.1:p.Asp1222His
NM_001382785.1:c.3649G>C	NP_001369714.1:p.Asp1217His
NM_001382786.1:c.3628G>C	NP_001369715.1:p.Asp1210His
NM_001382787.1:c.3622G>C	NP_001369716.1:p.Asp1208His
NM_001382788.1:c.3577G>C	NP_001369717.1:p.Asp1193His
NM_001382789.1:c.3568G>C	NP_001369718.1:p.Asp1190His
NM_001382790.1:c.3544G>C	NP_001369719.1:p.Asp1182His
NM_001382791.1:c.3538G>C	NP_001369720.1:p.Asp1180His
NM_001382792.1:c.3511G>C	NP_001369721.1:p.Asp1171His
NM_001382793.1:c.3505G>C	NP_001369722.1:p.Asp1169His
NM_001382794.1:c.3505G>C	NP_001369723.1:p.Asp1169His
NM_001382795.1:c.3499G>C	NP_001369724.1:p.Asp1167His
NM_001382796.1:c.3460G>C	NP_001369725.1:p.Asp1154His
NM_001382797.1:c.3448G>C	NP_001369726.1:p.Asp1150His
NM_001382798.1:c.3391G>C	NP_001369727.1:p.Asp1131His
NM_001382799.1:c.3367G>C	NP_001369728.1:p.Asp1123His
NM_001382800.1:c.3361G>C	NP_001369729.1:p.Asp1121His
NM_001382801.1:c.3343G>C	NP_001369730.1:p.Asp1115His
NM_001382802.1:c.3289G>C	NP_001369731.1:p.Asp1097His
NM_001382803.1:c.*126G>C	NP_001369732.1:n.*126G>C
NM_001382804.1:c.2719G>C	NP_001369733.1:p.Asp907His
NM_001382805.1:c.2596G>C	NP_001369734.1:p.Asp866His
NM_001382806.1:c.2509G>C	NP_001369735.1:p.Asp837His
NM_004448.4:c.3547G>C MANE Select	NP_004439.2:p.Asp1183His
NR_110535.2:n.3785G>C