Canonical Allele Identifier: CA399310558

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143243045
• MyVariant Identifiers: chr17:g.37883644T>A (hg19) ; chr17:g.39727391T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727391T>A , CM000679.2:g.39727391T>A	GRCh38
NC_000017.10:g.37883644T>A , CM000679.1:g.37883644T>A	GRCh37
NC_000017.9:g.35137170T>A	NCBI36
NG_007503.1:g.44252T>A , LRG_724:g.44252T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3256T>A MANE Select	ENSP00000269571.4:p.Phe1086Ile
ENST00000269571.9:c.3256T>A	ENSP00000269571.4:p.Phe1086Ile
ENST00000406381.6:c.3166T>A	ENSP00000385185.2:p.Phe1056Ile
ENST00000445658.6:c.2428T>A	ENSP00000404047.2:p.Phe810Ile
ENST00000541774.5:c.3211T>A	ENSP00000446466.1:p.Phe1071Ile
ENST00000578373.5:c.*3046T>A	ENSP00000463427.1:n.*3046T>A
ENST00000584450.5:c.3160-298T>A	ENSP00000463714.1:n.3160-298T>A
ENST00000584601.5:c.3166T>A	ENSP00000462438.1:p.Phe1056Ile
NM_001005862.2:c.3166T>A , LRG_724t1:c.3166T>A	NP_001005862.1:p.Phe1056Ile
NM_001289936.1:c.3211T>A , LRG_724t4:c.3211T>A	NP_001276865.1:p.Phe1071Ile
NM_001289937.1:c.3160-298T>A	NP_001276866.1:n.3160-298T>A
NM_004448.3:c.3256T>A , LRG_724t2:c.3256T>A	NP_004439.2:p.Phe1086Ile
NR_110535.1:n.3580T>A
XM_024450641.1:c.3394T>A	XP_024306409.1:p.Phe1132Ile
XM_024450642.1:c.3349T>A	XP_024306410.1:p.Phe1117Ile
XM_024450643.1:c.3304T>A	XP_024306411.1:p.Phe1102Ile
NM_001005862.3:c.3166T>A	NP_001005862.1:p.Phe1056Ile
NM_001289936.2:c.3211T>A	NP_001276865.1:p.Phe1071Ile
NM_001289937.2:c.3160-298T>A	NP_001276866.1:n.3160-298T>A
NM_001382782.1:c.3166T>A	NP_001369711.1:p.Phe1056Ile
NM_001382783.1:c.3166T>A	NP_001369712.1:p.Phe1056Ile
NM_001382784.1:c.3373T>A	NP_001369713.1:p.Phe1125Ile
NM_001382785.1:c.3358T>A	NP_001369714.1:p.Phe1120Ile
NM_001382786.1:c.3337T>A	NP_001369715.1:p.Phe1113Ile
NM_001382787.1:c.3331T>A	NP_001369716.1:p.Phe1111Ile
NM_001382788.1:c.3286T>A	NP_001369717.1:p.Phe1096Ile
NM_001382789.1:c.3277T>A	NP_001369718.1:p.Phe1093Ile
NM_001382790.1:c.3253T>A	NP_001369719.1:p.Phe1085Ile
NM_001382791.1:c.3247T>A	NP_001369720.1:p.Phe1083Ile
NM_001382792.1:c.3220T>A	NP_001369721.1:p.Phe1074Ile
NM_001382793.1:c.3214T>A	NP_001369722.1:p.Phe1072Ile
NM_001382794.1:c.3214T>A	NP_001369723.1:p.Phe1072Ile
NM_001382795.1:c.3208T>A	NP_001369724.1:p.Phe1070Ile
NM_001382796.1:c.3169T>A	NP_001369725.1:p.Phe1057Ile
NM_001382797.1:c.3157T>A	NP_001369726.1:p.Phe1053Ile
NM_001382798.1:c.3100T>A	NP_001369727.1:p.Phe1034Ile
NM_001382799.1:c.3076T>A	NP_001369728.1:p.Phe1026Ile
NM_001382800.1:c.3070T>A	NP_001369729.1:p.Phe1024Ile
NM_001382801.1:c.3052T>A	NP_001369730.1:p.Phe1018Ile
NM_001382802.1:c.2998T>A	NP_001369731.1:p.Phe1000Ile
NM_001382803.1:c.3118-298T>A	NP_001369732.1:n.3118-298T>A
NM_001382804.1:c.2428T>A	NP_001369733.1:p.Phe810Ile
NM_001382805.1:c.2305T>A	NP_001369734.1:p.Phe769Ile
NM_001382806.1:c.2218T>A	NP_001369735.1:p.Phe740Ile
NM_004448.4:c.3256T>A MANE Select	NP_004439.2:p.Phe1086Ile
NR_110535.2:n.3494T>A