Canonical Allele Identifier: CA399313573

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143302147
• MyVariant Identifiers: chr17:g.37884088T>A (hg19) ; chr17:g.39727835T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727835T>A , CM000679.2:g.39727835T>A	GRCh38
NC_000017.10:g.37884088T>A , CM000679.1:g.37884088T>A	GRCh37
NC_000017.9:g.35137614T>A	NCBI36
NG_007503.1:g.44696T>A , LRG_724:g.44696T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3559T>A MANE Select	ENSP00000269571.4:p.Phe1187Ile
ENST00000269571.9:c.3559T>A	ENSP00000269571.4:p.Phe1187Ile
ENST00000406381.6:c.3469T>A	ENSP00000385185.2:p.Phe1157Ile
ENST00000445658.6:c.2731T>A	ENSP00000404047.2:p.Phe911Ile
ENST00000541774.5:c.3514T>A	ENSP00000446466.1:p.Phe1172Ile
ENST00000578373.5:c.*3349T>A	ENSP00000463427.1:n.*3349T>A
ENST00000584450.5:c.*138T>A	ENSP00000463714.1:n.*138T>A
ENST00000584601.5:c.3469T>A	ENSP00000462438.1:p.Phe1157Ile
NM_001005862.2:c.3469T>A , LRG_724t1:c.3469T>A	NP_001005862.1:p.Phe1157Ile
NM_001289936.1:c.3514T>A , LRG_724t4:c.3514T>A	NP_001276865.1:p.Phe1172Ile
NM_001289937.1:c.*138T>A	NP_001276866.1:n.*138T>A
NM_004448.3:c.3559T>A , LRG_724t2:c.3559T>A	NP_004439.2:p.Phe1187Ile
NR_110535.1:n.3883T>A
XM_024450641.1:c.3697T>A	XP_024306409.1:p.Phe1233Ile
XM_024450642.1:c.3652T>A	XP_024306410.1:p.Phe1218Ile
XM_024450643.1:c.3607T>A	XP_024306411.1:p.Phe1203Ile
NM_001005862.3:c.3469T>A	NP_001005862.1:p.Phe1157Ile
NM_001289936.2:c.3514T>A	NP_001276865.1:p.Phe1172Ile
NM_001289937.2:c.*138T>A	NP_001276866.1:n.*138T>A
NM_001382782.1:c.3469T>A	NP_001369711.1:p.Phe1157Ile
NM_001382783.1:c.3469T>A	NP_001369712.1:p.Phe1157Ile
NM_001382784.1:c.3676T>A	NP_001369713.1:p.Phe1226Ile
NM_001382785.1:c.3661T>A	NP_001369714.1:p.Phe1221Ile
NM_001382786.1:c.3640T>A	NP_001369715.1:p.Phe1214Ile
NM_001382787.1:c.3634T>A	NP_001369716.1:p.Phe1212Ile
NM_001382788.1:c.3589T>A	NP_001369717.1:p.Phe1197Ile
NM_001382789.1:c.3580T>A	NP_001369718.1:p.Phe1194Ile
NM_001382790.1:c.3556T>A	NP_001369719.1:p.Phe1186Ile
NM_001382791.1:c.3550T>A	NP_001369720.1:p.Phe1184Ile
NM_001382792.1:c.3523T>A	NP_001369721.1:p.Phe1175Ile
NM_001382793.1:c.3517T>A	NP_001369722.1:p.Phe1173Ile
NM_001382794.1:c.3517T>A	NP_001369723.1:p.Phe1173Ile
NM_001382795.1:c.3511T>A	NP_001369724.1:p.Phe1171Ile
NM_001382796.1:c.3472T>A	NP_001369725.1:p.Phe1158Ile
NM_001382797.1:c.3460T>A	NP_001369726.1:p.Phe1154Ile
NM_001382798.1:c.3403T>A	NP_001369727.1:p.Phe1135Ile
NM_001382799.1:c.3379T>A	NP_001369728.1:p.Phe1127Ile
NM_001382800.1:c.3373T>A	NP_001369729.1:p.Phe1125Ile
NM_001382801.1:c.3355T>A	NP_001369730.1:p.Phe1119Ile
NM_001382802.1:c.3301T>A	NP_001369731.1:p.Phe1101Ile
NM_001382803.1:c.*138T>A	NP_001369732.1:n.*138T>A
NM_001382804.1:c.2731T>A	NP_001369733.1:p.Phe911Ile
NM_001382805.1:c.2608T>A	NP_001369734.1:p.Phe870Ile
NM_001382806.1:c.2521T>A	NP_001369735.1:p.Phe841Ile
NM_004448.4:c.3559T>A MANE Select	NP_004439.2:p.Phe1187Ile
NR_110535.2:n.3797T>A