Canonical Allele Identifier: CA399313933

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143307385
• MyVariant Identifiers: chr17:g.37884137C>A (hg19) ; chr17:g.39727884C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727884C>A , CM000679.2:g.39727884C>A	GRCh38
NC_000017.10:g.37884137C>A , CM000679.1:g.37884137C>A	GRCh37
NC_000017.9:g.35137663C>A	NCBI36
NG_007503.1:g.44745C>A , LRG_724:g.44745C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3608C>A MANE Select	ENSP00000269571.4:p.Ala1203Asp
ENST00000269571.9:c.3608C>A	ENSP00000269571.4:p.Ala1203Asp
ENST00000406381.6:c.3518C>A	ENSP00000385185.2:p.Ala1173Asp
ENST00000445658.6:c.2780C>A	ENSP00000404047.2:p.Ala927Asp
ENST00000541774.5:c.3563C>A	ENSP00000446466.1:p.Ala1188Asp
ENST00000578373.5:c.*3398C>A	ENSP00000463427.1:n.*3398C>A
ENST00000584450.5:c.*187C>A	ENSP00000463714.1:n.*187C>A
ENST00000584601.5:c.3518C>A	ENSP00000462438.1:p.Ala1173Asp
NM_001005862.2:c.3518C>A , LRG_724t1:c.3518C>A	NP_001005862.1:p.Ala1173Asp
NM_001289936.1:c.3563C>A , LRG_724t4:c.3563C>A	NP_001276865.1:p.Ala1188Asp
NM_001289937.1:c.*187C>A	NP_001276866.1:n.*187C>A
NM_004448.3:c.3608C>A , LRG_724t2:c.3608C>A	NP_004439.2:p.Ala1203Asp
NR_110535.1:n.3932C>A
XM_024450641.1:c.3746C>A	XP_024306409.1:p.Ala1249Asp
XM_024450642.1:c.3701C>A	XP_024306410.1:p.Ala1234Asp
XM_024450643.1:c.3656C>A	XP_024306411.1:p.Ala1219Asp
NM_001005862.3:c.3518C>A	NP_001005862.1:p.Ala1173Asp
NM_001289936.2:c.3563C>A	NP_001276865.1:p.Ala1188Asp
NM_001289937.2:c.*187C>A	NP_001276866.1:n.*187C>A
NM_001382782.1:c.3518C>A	NP_001369711.1:p.Ala1173Asp
NM_001382783.1:c.3518C>A	NP_001369712.1:p.Ala1173Asp
NM_001382784.1:c.3725C>A	NP_001369713.1:p.Ala1242Asp
NM_001382785.1:c.3710C>A	NP_001369714.1:p.Ala1237Asp
NM_001382786.1:c.3689C>A	NP_001369715.1:p.Ala1230Asp
NM_001382787.1:c.3683C>A	NP_001369716.1:p.Ala1228Asp
NM_001382788.1:c.3638C>A	NP_001369717.1:p.Ala1213Asp
NM_001382789.1:c.3629C>A	NP_001369718.1:p.Ala1210Asp
NM_001382790.1:c.3605C>A	NP_001369719.1:p.Ala1202Asp
NM_001382791.1:c.3599C>A	NP_001369720.1:p.Ala1200Asp
NM_001382792.1:c.3572C>A	NP_001369721.1:p.Ala1191Asp
NM_001382793.1:c.3566C>A	NP_001369722.1:p.Ala1189Asp
NM_001382794.1:c.3566C>A	NP_001369723.1:p.Ala1189Asp
NM_001382795.1:c.3560C>A	NP_001369724.1:p.Ala1187Asp
NM_001382796.1:c.3521C>A	NP_001369725.1:p.Ala1174Asp
NM_001382797.1:c.3509C>A	NP_001369726.1:p.Ala1170Asp
NM_001382798.1:c.3452C>A	NP_001369727.1:p.Ala1151Asp
NM_001382799.1:c.3428C>A	NP_001369728.1:p.Ala1143Asp
NM_001382800.1:c.3422C>A	NP_001369729.1:p.Ala1141Asp
NM_001382801.1:c.3404C>A	NP_001369730.1:p.Ala1135Asp
NM_001382802.1:c.3350C>A	NP_001369731.1:p.Ala1117Asp
NM_001382803.1:c.*187C>A	NP_001369732.1:n.*187C>A
NM_001382804.1:c.2780C>A	NP_001369733.1:p.Ala927Asp
NM_001382805.1:c.2657C>A	NP_001369734.1:p.Ala886Asp
NM_001382806.1:c.2570C>A	NP_001369735.1:p.Ala857Asp
NM_004448.4:c.3608C>A MANE Select	NP_004439.2:p.Ala1203Asp
NR_110535.2:n.3846C>A