Canonical Allele Identifier: CA499890768

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143305390
• MyVariant Identifiers: chr17:g.37884118T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727865T>C , CM000679.2:g.39727865T>C	GRCh38
NC_000017.10:g.37884118T>C , CM000679.1:g.37884118T>C	GRCh37
NC_000017.9:g.35137644T>C	NCBI36
NG_007503.1:g.44726T>C , LRG_724:g.44726T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3589T>C MANE Select	ENSP00000269571.4:p.Leu1197=
ENST00000269571.9:c.3589T>C	ENSP00000269571.4:p.Leu1197=
ENST00000406381.6:c.3499T>C	ENSP00000385185.2:p.Leu1167=
ENST00000445658.6:c.2761T>C	ENSP00000404047.2:p.Leu921=
ENST00000541774.5:c.3544T>C	ENSP00000446466.1:p.Leu1182=
ENST00000578373.5:c.*3379T>C	ENSP00000463427.1:n.*3379T>C
ENST00000584450.5:c.*168T>C	ENSP00000463714.1:n.*168T>C
ENST00000584601.5:c.3499T>C	ENSP00000462438.1:p.Leu1167=
NM_001005862.2:c.3499T>C , LRG_724t1:c.3499T>C	NP_001005862.1:p.Leu1167=
NM_001289936.1:c.3544T>C , LRG_724t4:c.3544T>C	NP_001276865.1:p.Leu1182=
NM_001289937.1:c.*168T>C	NP_001276866.1:n.*168T>C
NM_004448.3:c.3589T>C , LRG_724t2:c.3589T>C	NP_004439.2:p.Leu1197=
NR_110535.1:n.3913T>C
XM_024450641.1:c.3727T>C	XP_024306409.1:p.Leu1243=
XM_024450642.1:c.3682T>C	XP_024306410.1:p.Leu1228=
XM_024450643.1:c.3637T>C	XP_024306411.1:p.Leu1213=
NM_001005862.3:c.3499T>C	NP_001005862.1:p.Leu1167=
NM_001289936.2:c.3544T>C	NP_001276865.1:p.Leu1182=
NM_001289937.2:c.*168T>C	NP_001276866.1:n.*168T>C
NM_001382782.1:c.3499T>C	NP_001369711.1:p.Leu1167=
NM_001382783.1:c.3499T>C	NP_001369712.1:p.Leu1167=
NM_001382784.1:c.3706T>C	NP_001369713.1:p.Leu1236=
NM_001382785.1:c.3691T>C	NP_001369714.1:p.Leu1231=
NM_001382786.1:c.3670T>C	NP_001369715.1:p.Leu1224=
NM_001382787.1:c.3664T>C	NP_001369716.1:p.Leu1222=
NM_001382788.1:c.3619T>C	NP_001369717.1:p.Leu1207=
NM_001382789.1:c.3610T>C	NP_001369718.1:p.Leu1204=
NM_001382790.1:c.3586T>C	NP_001369719.1:p.Leu1196=
NM_001382791.1:c.3580T>C	NP_001369720.1:p.Leu1194=
NM_001382792.1:c.3553T>C	NP_001369721.1:p.Leu1185=
NM_001382793.1:c.3547T>C	NP_001369722.1:p.Leu1183=
NM_001382794.1:c.3547T>C	NP_001369723.1:p.Leu1183=
NM_001382795.1:c.3541T>C	NP_001369724.1:p.Leu1181=
NM_001382796.1:c.3502T>C	NP_001369725.1:p.Leu1168=
NM_001382797.1:c.3490T>C	NP_001369726.1:p.Leu1164=
NM_001382798.1:c.3433T>C	NP_001369727.1:p.Leu1145=
NM_001382799.1:c.3409T>C	NP_001369728.1:p.Leu1137=
NM_001382800.1:c.3403T>C	NP_001369729.1:p.Leu1135=
NM_001382801.1:c.3385T>C	NP_001369730.1:p.Leu1129=
NM_001382802.1:c.3331T>C	NP_001369731.1:p.Leu1111=
NM_001382803.1:c.*168T>C	NP_001369732.1:n.*168T>C
NM_001382804.1:c.2761T>C	NP_001369733.1:p.Leu921=
NM_001382805.1:c.2638T>C	NP_001369734.1:p.Leu880=
NM_001382806.1:c.2551T>C	NP_001369735.1:p.Leu851=
NM_004448.4:c.3589T>C MANE Select	NP_004439.2:p.Leu1197=
NR_110535.2:n.3827T>C