Canonical Allele Identifier: CA399310421

Gene: ERBB2

Linked Data

• dbSNP Id: rs748800582
• MyVariant Identifiers: chr17:g.37883621C>A (hg19) ; chr17:g.39727368C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727368C>A , CM000679.2:g.39727368C>A	GRCh38
NC_000017.10:g.37883621C>A , CM000679.1:g.37883621C>A	GRCh37
NC_000017.9:g.35137147C>A	NCBI36
NG_007503.1:g.44229C>A , LRG_724:g.44229C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3233C>A MANE Select	ENSP00000269571.4:p.Ser1078Tyr
ENST00000269571.9:c.3233C>A	ENSP00000269571.4:p.Ser1078Tyr
ENST00000406381.6:c.3143C>A	ENSP00000385185.2:p.Ser1048Tyr
ENST00000445658.6:c.2405C>A	ENSP00000404047.2:p.Ser802Tyr
ENST00000541774.5:c.3188C>A	ENSP00000446466.1:p.Ser1063Tyr
ENST00000578373.5:c.*3023C>A	ENSP00000463427.1:n.*3023C>A
ENST00000584450.5:c.3160-321C>A	ENSP00000463714.1:n.3160-321C>A
ENST00000584601.5:c.3143C>A	ENSP00000462438.1:p.Ser1048Tyr
NM_001005862.2:c.3143C>A , LRG_724t1:c.3143C>A	NP_001005862.1:p.Ser1048Tyr
NM_001289936.1:c.3188C>A , LRG_724t4:c.3188C>A	NP_001276865.1:p.Ser1063Tyr
NM_001289937.1:c.3160-321C>A	NP_001276866.1:n.3160-321C>A
NM_004448.3:c.3233C>A , LRG_724t2:c.3233C>A	NP_004439.2:p.Ser1078Tyr
NR_110535.1:n.3557C>A
XM_024450641.1:c.3371C>A	XP_024306409.1:p.Ser1124Tyr
XM_024450642.1:c.3326C>A	XP_024306410.1:p.Ser1109Tyr
XM_024450643.1:c.3281C>A	XP_024306411.1:p.Ser1094Tyr
NM_001005862.3:c.3143C>A	NP_001005862.1:p.Ser1048Tyr
NM_001289936.2:c.3188C>A	NP_001276865.1:p.Ser1063Tyr
NM_001289937.2:c.3160-321C>A	NP_001276866.1:n.3160-321C>A
NM_001382782.1:c.3143C>A	NP_001369711.1:p.Ser1048Tyr
NM_001382783.1:c.3143C>A	NP_001369712.1:p.Ser1048Tyr
NM_001382784.1:c.3350C>A	NP_001369713.1:p.Ser1117Tyr
NM_001382785.1:c.3335C>A	NP_001369714.1:p.Ser1112Tyr
NM_001382786.1:c.3314C>A	NP_001369715.1:p.Ser1105Tyr
NM_001382787.1:c.3308C>A	NP_001369716.1:p.Ser1103Tyr
NM_001382788.1:c.3263C>A	NP_001369717.1:p.Ser1088Tyr
NM_001382789.1:c.3254C>A	NP_001369718.1:p.Ser1085Tyr
NM_001382790.1:c.3230C>A	NP_001369719.1:p.Ser1077Tyr
NM_001382791.1:c.3224C>A	NP_001369720.1:p.Ser1075Tyr
NM_001382792.1:c.3197C>A	NP_001369721.1:p.Ser1066Tyr
NM_001382793.1:c.3191C>A	NP_001369722.1:p.Ser1064Tyr
NM_001382794.1:c.3191C>A	NP_001369723.1:p.Ser1064Tyr
NM_001382795.1:c.3185C>A	NP_001369724.1:p.Ser1062Tyr
NM_001382796.1:c.3146C>A	NP_001369725.1:p.Ser1049Tyr
NM_001382797.1:c.3134C>A	NP_001369726.1:p.Ser1045Tyr
NM_001382798.1:c.3077C>A	NP_001369727.1:p.Ser1026Tyr
NM_001382799.1:c.3053C>A	NP_001369728.1:p.Ser1018Tyr
NM_001382800.1:c.3047C>A	NP_001369729.1:p.Ser1016Tyr
NM_001382801.1:c.3029C>A	NP_001369730.1:p.Ser1010Tyr
NM_001382802.1:c.2975C>A	NP_001369731.1:p.Ser992Tyr
NM_001382803.1:c.3118-321C>A	NP_001369732.1:n.3118-321C>A
NM_001382804.1:c.2405C>A	NP_001369733.1:p.Ser802Tyr
NM_001382805.1:c.2282C>A	NP_001369734.1:p.Ser761Tyr
NM_001382806.1:c.2195C>A	NP_001369735.1:p.Ser732Tyr
NM_004448.4:c.3233C>A MANE Select	NP_004439.2:p.Ser1078Tyr
NR_110535.2:n.3471C>A