Canonical Allele Identifier: CA399314253

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884178T>G (hg19) ; chr17:g.39727925T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727925T>G , CM000679.2:g.39727925T>G	GRCh38
NC_000017.10:g.37884178T>G , CM000679.1:g.37884178T>G	GRCh37
NC_000017.9:g.35137704T>G	NCBI36
NG_007503.1:g.44786T>G , LRG_724:g.44786T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3649T>G MANE Select	ENSP00000269571.4:p.Phe1217Val
ENST00000269571.9:c.3649T>G	ENSP00000269571.4:p.Phe1217Val
ENST00000406381.6:c.3559T>G	ENSP00000385185.2:p.Phe1187Val
ENST00000445658.6:c.2821T>G	ENSP00000404047.2:p.Phe941Val
ENST00000541774.5:c.3604T>G	ENSP00000446466.1:p.Phe1202Val
ENST00000578373.5:c.*3439T>G	ENSP00000463427.1:n.*3439T>G
ENST00000584450.5:c.*228T>G	ENSP00000463714.1:n.*228T>G
ENST00000584601.5:c.3559T>G	ENSP00000462438.1:p.Phe1187Val
NM_001005862.2:c.3559T>G , LRG_724t1:c.3559T>G	NP_001005862.1:p.Phe1187Val
NM_001289936.1:c.3604T>G , LRG_724t4:c.3604T>G	NP_001276865.1:p.Phe1202Val
NM_001289937.1:c.*228T>G	NP_001276866.1:n.*228T>G
NM_004448.3:c.3649T>G , LRG_724t2:c.3649T>G	NP_004439.2:p.Phe1217Val
NR_110535.1:n.3973T>G
XM_024450641.1:c.3787T>G	XP_024306409.1:p.Phe1263Val
XM_024450642.1:c.3742T>G	XP_024306410.1:p.Phe1248Val
XM_024450643.1:c.3697T>G	XP_024306411.1:p.Phe1233Val
NM_001005862.3:c.3559T>G	NP_001005862.1:p.Phe1187Val
NM_001289936.2:c.3604T>G	NP_001276865.1:p.Phe1202Val
NM_001289937.2:c.*228T>G	NP_001276866.1:n.*228T>G
NM_001382782.1:c.3559T>G	NP_001369711.1:p.Phe1187Val
NM_001382783.1:c.3559T>G	NP_001369712.1:p.Phe1187Val
NM_001382784.1:c.3766T>G	NP_001369713.1:p.Phe1256Val
NM_001382785.1:c.3751T>G	NP_001369714.1:p.Phe1251Val
NM_001382786.1:c.3730T>G	NP_001369715.1:p.Phe1244Val
NM_001382787.1:c.3724T>G	NP_001369716.1:p.Phe1242Val
NM_001382788.1:c.3679T>G	NP_001369717.1:p.Phe1227Val
NM_001382789.1:c.3670T>G	NP_001369718.1:p.Phe1224Val
NM_001382790.1:c.3646T>G	NP_001369719.1:p.Phe1216Val
NM_001382791.1:c.3640T>G	NP_001369720.1:p.Phe1214Val
NM_001382792.1:c.3613T>G	NP_001369721.1:p.Phe1205Val
NM_001382793.1:c.3607T>G	NP_001369722.1:p.Phe1203Val
NM_001382794.1:c.3607T>G	NP_001369723.1:p.Phe1203Val
NM_001382795.1:c.3601T>G	NP_001369724.1:p.Phe1201Val
NM_001382796.1:c.3562T>G	NP_001369725.1:p.Phe1188Val
NM_001382797.1:c.3550T>G	NP_001369726.1:p.Phe1184Val
NM_001382798.1:c.3493T>G	NP_001369727.1:p.Phe1165Val
NM_001382799.1:c.3469T>G	NP_001369728.1:p.Phe1157Val
NM_001382800.1:c.3463T>G	NP_001369729.1:p.Phe1155Val
NM_001382801.1:c.3445T>G	NP_001369730.1:p.Phe1149Val
NM_001382802.1:c.3391T>G	NP_001369731.1:p.Phe1131Val
NM_001382803.1:c.*228T>G	NP_001369732.1:n.*228T>G
NM_001382804.1:c.2821T>G	NP_001369733.1:p.Phe941Val
NM_001382805.1:c.2698T>G	NP_001369734.1:p.Phe900Val
NM_001382806.1:c.2611T>G	NP_001369735.1:p.Phe871Val
NM_004448.4:c.3649T>G MANE Select	NP_004439.2:p.Phe1217Val
NR_110535.2:n.3887T>G