Canonical Allele Identifier: CA399313815

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143305390
• MyVariant Identifiers: chr17:g.37884118T>A (hg19) ; chr17:g.39727865T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3589T>A MANE Select	ENSP00000269571.4:p.Leu1197Met
ENST00000269571.9:c.3589T>A	ENSP00000269571.4:p.Leu1197Met
ENST00000406381.6:c.3499T>A	ENSP00000385185.2:p.Leu1167Met
ENST00000445658.6:c.2761T>A	ENSP00000404047.2:p.Leu921Met
ENST00000541774.5:c.3544T>A	ENSP00000446466.1:p.Leu1182Met
ENST00000578373.5:c.*3379T>A	ENSP00000463427.1:n.*3379T>A
ENST00000584450.5:c.*168T>A	ENSP00000463714.1:n.*168T>A
ENST00000584601.5:c.3499T>A	ENSP00000462438.1:p.Leu1167Met
NM_001005862.2:c.3499T>A , LRG_724t1:c.3499T>A	NP_001005862.1:p.Leu1167Met
NM_001289936.1:c.3544T>A , LRG_724t4:c.3544T>A	NP_001276865.1:p.Leu1182Met
NM_001289937.1:c.*168T>A	NP_001276866.1:n.*168T>A
NM_004448.3:c.3589T>A , LRG_724t2:c.3589T>A	NP_004439.2:p.Leu1197Met
NR_110535.1:n.3913T>A
XM_024450641.1:c.3727T>A	XP_024306409.1:p.Leu1243Met
XM_024450642.1:c.3682T>A	XP_024306410.1:p.Leu1228Met
XM_024450643.1:c.3637T>A	XP_024306411.1:p.Leu1213Met
NM_001005862.3:c.3499T>A	NP_001005862.1:p.Leu1167Met
NM_001289936.2:c.3544T>A	NP_001276865.1:p.Leu1182Met
NM_001289937.2:c.*168T>A	NP_001276866.1:n.*168T>A
NM_001382782.1:c.3499T>A	NP_001369711.1:p.Leu1167Met
NM_001382783.1:c.3499T>A	NP_001369712.1:p.Leu1167Met
NM_001382784.1:c.3706T>A	NP_001369713.1:p.Leu1236Met
NM_001382785.1:c.3691T>A	NP_001369714.1:p.Leu1231Met
NM_001382786.1:c.3670T>A	NP_001369715.1:p.Leu1224Met
NM_001382787.1:c.3664T>A	NP_001369716.1:p.Leu1222Met
NM_001382788.1:c.3619T>A	NP_001369717.1:p.Leu1207Met
NM_001382789.1:c.3610T>A	NP_001369718.1:p.Leu1204Met
NM_001382790.1:c.3586T>A	NP_001369719.1:p.Leu1196Met
NM_001382791.1:c.3580T>A	NP_001369720.1:p.Leu1194Met
NM_001382792.1:c.3553T>A	NP_001369721.1:p.Leu1185Met
NM_001382793.1:c.3547T>A	NP_001369722.1:p.Leu1183Met
NM_001382794.1:c.3547T>A	NP_001369723.1:p.Leu1183Met
NM_001382795.1:c.3541T>A	NP_001369724.1:p.Leu1181Met
NM_001382796.1:c.3502T>A	NP_001369725.1:p.Leu1168Met
NM_001382797.1:c.3490T>A	NP_001369726.1:p.Leu1164Met
NM_001382798.1:c.3433T>A	NP_001369727.1:p.Leu1145Met
NM_001382799.1:c.3409T>A	NP_001369728.1:p.Leu1137Met
NM_001382800.1:c.3403T>A	NP_001369729.1:p.Leu1135Met
NM_001382801.1:c.3385T>A	NP_001369730.1:p.Leu1129Met
NM_001382802.1:c.3331T>A	NP_001369731.1:p.Leu1111Met
NM_001382803.1:c.*168T>A	NP_001369732.1:n.*168T>A
NM_001382804.1:c.2761T>A	NP_001369733.1:p.Leu921Met
NM_001382805.1:c.2638T>A	NP_001369734.1:p.Leu880Met
NM_001382806.1:c.2551T>A	NP_001369735.1:p.Leu851Met
NM_004448.4:c.3589T>A MANE Select	NP_004439.2:p.Leu1197Met
NR_110535.2:n.3827T>A