Canonical Allele Identifier: CA399313482

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3547G>A MANE Select	ENSP00000269571.4:p.Asp1183Asn
ENST00000269571.9:c.3547G>A	ENSP00000269571.4:p.Asp1183Asn
ENST00000406381.6:c.3457G>A	ENSP00000385185.2:p.Asp1153Asn
ENST00000445658.6:c.2719G>A	ENSP00000404047.2:p.Asp907Asn
ENST00000541774.5:c.3502G>A	ENSP00000446466.1:p.Asp1168Asn
ENST00000578373.5:c.*3337G>A	ENSP00000463427.1:n.*3337G>A
ENST00000584450.5:c.*126G>A	ENSP00000463714.1:n.*126G>A
ENST00000584601.5:c.3457G>A	ENSP00000462438.1:p.Asp1153Asn
NM_001005862.2:c.3457G>A , LRG_724t1:c.3457G>A	NP_001005862.1:p.Asp1153Asn
NM_001289936.1:c.3502G>A , LRG_724t4:c.3502G>A	NP_001276865.1:p.Asp1168Asn
NM_001289937.1:c.*126G>A	NP_001276866.1:n.*126G>A
NM_004448.3:c.3547G>A , LRG_724t2:c.3547G>A	NP_004439.2:p.Asp1183Asn
NR_110535.1:n.3871G>A
XM_024450641.1:c.3685G>A	XP_024306409.1:p.Asp1229Asn
XM_024450642.1:c.3640G>A	XP_024306410.1:p.Asp1214Asn
XM_024450643.1:c.3595G>A	XP_024306411.1:p.Asp1199Asn
NM_001005862.3:c.3457G>A	NP_001005862.1:p.Asp1153Asn
NM_001289936.2:c.3502G>A	NP_001276865.1:p.Asp1168Asn
NM_001289937.2:c.*126G>A	NP_001276866.1:n.*126G>A
NM_001382782.1:c.3457G>A	NP_001369711.1:p.Asp1153Asn
NM_001382783.1:c.3457G>A	NP_001369712.1:p.Asp1153Asn
NM_001382784.1:c.3664G>A	NP_001369713.1:p.Asp1222Asn
NM_001382785.1:c.3649G>A	NP_001369714.1:p.Asp1217Asn
NM_001382786.1:c.3628G>A	NP_001369715.1:p.Asp1210Asn
NM_001382787.1:c.3622G>A	NP_001369716.1:p.Asp1208Asn
NM_001382788.1:c.3577G>A	NP_001369717.1:p.Asp1193Asn
NM_001382789.1:c.3568G>A	NP_001369718.1:p.Asp1190Asn
NM_001382790.1:c.3544G>A	NP_001369719.1:p.Asp1182Asn
NM_001382791.1:c.3538G>A	NP_001369720.1:p.Asp1180Asn
NM_001382792.1:c.3511G>A	NP_001369721.1:p.Asp1171Asn
NM_001382793.1:c.3505G>A	NP_001369722.1:p.Asp1169Asn
NM_001382794.1:c.3505G>A	NP_001369723.1:p.Asp1169Asn
NM_001382795.1:c.3499G>A	NP_001369724.1:p.Asp1167Asn
NM_001382796.1:c.3460G>A	NP_001369725.1:p.Asp1154Asn
NM_001382797.1:c.3448G>A	NP_001369726.1:p.Asp1150Asn
NM_001382798.1:c.3391G>A	NP_001369727.1:p.Asp1131Asn
NM_001382799.1:c.3367G>A	NP_001369728.1:p.Asp1123Asn
NM_001382800.1:c.3361G>A	NP_001369729.1:p.Asp1121Asn
NM_001382801.1:c.3343G>A	NP_001369730.1:p.Asp1115Asn
NM_001382802.1:c.3289G>A	NP_001369731.1:p.Asp1097Asn
NM_001382803.1:c.*126G>A	NP_001369732.1:n.*126G>A
NM_001382804.1:c.2719G>A	NP_001369733.1:p.Asp907Asn
NM_001382805.1:c.2596G>A	NP_001369734.1:p.Asp866Asn
NM_001382806.1:c.2509G>A	NP_001369735.1:p.Asp837Asn
NM_004448.4:c.3547G>A MANE Select	NP_004439.2:p.Asp1183Asn
NR_110535.2:n.3785G>A