Canonical Allele Identifier: CA399310476

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143241033
• MyVariant Identifiers: chr17:g.37883630C>A (hg19) ; chr17:g.39727377C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727377C>A , CM000679.2:g.39727377C>A	GRCh38
NC_000017.10:g.37883630C>A , CM000679.1:g.37883630C>A	GRCh37
NC_000017.9:g.35137156C>A	NCBI36
NG_007503.1:g.44238C>A , LRG_724:g.44238C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3242C>A MANE Select	ENSP00000269571.4:p.Ala1081Asp
ENST00000269571.9:c.3242C>A	ENSP00000269571.4:p.Ala1081Asp
ENST00000406381.6:c.3152C>A	ENSP00000385185.2:p.Ala1051Asp
ENST00000445658.6:c.2414C>A	ENSP00000404047.2:p.Ala805Asp
ENST00000541774.5:c.3197C>A	ENSP00000446466.1:p.Ala1066Asp
ENST00000578373.5:c.*3032C>A	ENSP00000463427.1:n.*3032C>A
ENST00000584450.5:c.3160-312C>A	ENSP00000463714.1:n.3160-312C>A
ENST00000584601.5:c.3152C>A	ENSP00000462438.1:p.Ala1051Asp
NM_001005862.2:c.3152C>A , LRG_724t1:c.3152C>A	NP_001005862.1:p.Ala1051Asp
NM_001289936.1:c.3197C>A , LRG_724t4:c.3197C>A	NP_001276865.1:p.Ala1066Asp
NM_001289937.1:c.3160-312C>A	NP_001276866.1:n.3160-312C>A
NM_004448.3:c.3242C>A , LRG_724t2:c.3242C>A	NP_004439.2:p.Ala1081Asp
NR_110535.1:n.3566C>A
XM_024450641.1:c.3380C>A	XP_024306409.1:p.Ala1127Asp
XM_024450642.1:c.3335C>A	XP_024306410.1:p.Ala1112Asp
XM_024450643.1:c.3290C>A	XP_024306411.1:p.Ala1097Asp
NM_001005862.3:c.3152C>A	NP_001005862.1:p.Ala1051Asp
NM_001289936.2:c.3197C>A	NP_001276865.1:p.Ala1066Asp
NM_001289937.2:c.3160-312C>A	NP_001276866.1:n.3160-312C>A
NM_001382782.1:c.3152C>A	NP_001369711.1:p.Ala1051Asp
NM_001382783.1:c.3152C>A	NP_001369712.1:p.Ala1051Asp
NM_001382784.1:c.3359C>A	NP_001369713.1:p.Ala1120Asp
NM_001382785.1:c.3344C>A	NP_001369714.1:p.Ala1115Asp
NM_001382786.1:c.3323C>A	NP_001369715.1:p.Ala1108Asp
NM_001382787.1:c.3317C>A	NP_001369716.1:p.Ala1106Asp
NM_001382788.1:c.3272C>A	NP_001369717.1:p.Ala1091Asp
NM_001382789.1:c.3263C>A	NP_001369718.1:p.Ala1088Asp
NM_001382790.1:c.3239C>A	NP_001369719.1:p.Ala1080Asp
NM_001382791.1:c.3233C>A	NP_001369720.1:p.Ala1078Asp
NM_001382792.1:c.3206C>A	NP_001369721.1:p.Ala1069Asp
NM_001382793.1:c.3200C>A	NP_001369722.1:p.Ala1067Asp
NM_001382794.1:c.3200C>A	NP_001369723.1:p.Ala1067Asp
NM_001382795.1:c.3194C>A	NP_001369724.1:p.Ala1065Asp
NM_001382796.1:c.3155C>A	NP_001369725.1:p.Ala1052Asp
NM_001382797.1:c.3143C>A	NP_001369726.1:p.Ala1048Asp
NM_001382798.1:c.3086C>A	NP_001369727.1:p.Ala1029Asp
NM_001382799.1:c.3062C>A	NP_001369728.1:p.Ala1021Asp
NM_001382800.1:c.3056C>A	NP_001369729.1:p.Ala1019Asp
NM_001382801.1:c.3038C>A	NP_001369730.1:p.Ala1013Asp
NM_001382802.1:c.2984C>A	NP_001369731.1:p.Ala995Asp
NM_001382803.1:c.3118-312C>A	NP_001369732.1:n.3118-312C>A
NM_001382804.1:c.2414C>A	NP_001369733.1:p.Ala805Asp
NM_001382805.1:c.2291C>A	NP_001369734.1:p.Ala764Asp
NM_001382806.1:c.2204C>A	NP_001369735.1:p.Ala735Asp
NM_004448.4:c.3242C>A MANE Select	NP_004439.2:p.Ala1081Asp
NR_110535.2:n.3480C>A