Canonical Allele Identifier: CA399314465

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884203A>T (hg19) ; chr17:g.39727950A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727950A>T , CM000679.2:g.39727950A>T	GRCh38
NC_000017.10:g.37884203A>T , CM000679.1:g.37884203A>T	GRCh37
NC_000017.9:g.35137729A>T	NCBI36
NG_007503.1:g.44811A>T , LRG_724:g.44811A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3674A>T MANE Select	ENSP00000269571.4:p.Gln1225Leu
ENST00000269571.9:c.3674A>T	ENSP00000269571.4:p.Gln1225Leu
ENST00000406381.6:c.3584A>T	ENSP00000385185.2:p.Gln1195Leu
ENST00000445658.6:c.2846A>T	ENSP00000404047.2:p.Gln949Leu
ENST00000541774.5:c.3629A>T	ENSP00000446466.1:p.Gln1210Leu
ENST00000578373.5:c.*3464A>T	ENSP00000463427.1:n.*3464A>T
ENST00000584450.5:c.*253A>T	ENSP00000463714.1:n.*253A>T
ENST00000584601.5:c.3584A>T	ENSP00000462438.1:p.Gln1195Leu
NM_001005862.2:c.3584A>T , LRG_724t1:c.3584A>T	NP_001005862.1:p.Gln1195Leu
NM_001289936.1:c.3629A>T , LRG_724t4:c.3629A>T	NP_001276865.1:p.Gln1210Leu
NM_001289937.1:c.*253A>T	NP_001276866.1:n.*253A>T
NM_004448.3:c.3674A>T , LRG_724t2:c.3674A>T	NP_004439.2:p.Gln1225Leu
NR_110535.1:n.3998A>T
XM_024450641.1:c.3812A>T	XP_024306409.1:p.Gln1271Leu
XM_024450642.1:c.3767A>T	XP_024306410.1:p.Gln1256Leu
XM_024450643.1:c.3722A>T	XP_024306411.1:p.Gln1241Leu
NM_001005862.3:c.3584A>T	NP_001005862.1:p.Gln1195Leu
NM_001289936.2:c.3629A>T	NP_001276865.1:p.Gln1210Leu
NM_001289937.2:c.*253A>T	NP_001276866.1:n.*253A>T
NM_001382782.1:c.3584A>T	NP_001369711.1:p.Gln1195Leu
NM_001382783.1:c.3584A>T	NP_001369712.1:p.Gln1195Leu
NM_001382784.1:c.3791A>T	NP_001369713.1:p.Gln1264Leu
NM_001382785.1:c.3776A>T	NP_001369714.1:p.Gln1259Leu
NM_001382786.1:c.3755A>T	NP_001369715.1:p.Gln1252Leu
NM_001382787.1:c.3749A>T	NP_001369716.1:p.Gln1250Leu
NM_001382788.1:c.3704A>T	NP_001369717.1:p.Gln1235Leu
NM_001382789.1:c.3695A>T	NP_001369718.1:p.Gln1232Leu
NM_001382790.1:c.3671A>T	NP_001369719.1:p.Gln1224Leu
NM_001382791.1:c.3665A>T	NP_001369720.1:p.Gln1222Leu
NM_001382792.1:c.3638A>T	NP_001369721.1:p.Gln1213Leu
NM_001382793.1:c.3632A>T	NP_001369722.1:p.Gln1211Leu
NM_001382794.1:c.3632A>T	NP_001369723.1:p.Gln1211Leu
NM_001382795.1:c.3626A>T	NP_001369724.1:p.Gln1209Leu
NM_001382796.1:c.3587A>T	NP_001369725.1:p.Gln1196Leu
NM_001382797.1:c.3575A>T	NP_001369726.1:p.Gln1192Leu
NM_001382798.1:c.3518A>T	NP_001369727.1:p.Gln1173Leu
NM_001382799.1:c.3494A>T	NP_001369728.1:p.Gln1165Leu
NM_001382800.1:c.3488A>T	NP_001369729.1:p.Gln1163Leu
NM_001382801.1:c.3470A>T	NP_001369730.1:p.Gln1157Leu
NM_001382802.1:c.3416A>T	NP_001369731.1:p.Gln1139Leu
NM_001382803.1:c.*253A>T	NP_001369732.1:n.*253A>T
NM_001382804.1:c.2846A>T	NP_001369733.1:p.Gln949Leu
NM_001382805.1:c.2723A>T	NP_001369734.1:p.Gln908Leu
NM_001382806.1:c.2636A>T	NP_001369735.1:p.Gln879Leu
NM_004448.4:c.3674A>T MANE Select	NP_004439.2:p.Gln1225Leu
NR_110535.2:n.3912A>T