Canonical Allele Identifier: CA399313783

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884114G>T (hg19) ; chr17:g.39727861G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727861G>T , CM000679.2:g.39727861G>T	GRCh38
NC_000017.10:g.37884114G>T , CM000679.1:g.37884114G>T	GRCh37
NC_000017.9:g.35137640G>T	NCBI36
NG_007503.1:g.44722G>T , LRG_724:g.44722G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3585G>T MANE Select	ENSP00000269571.4:p.Glu1195Asp
ENST00000269571.9:c.3585G>T	ENSP00000269571.4:p.Glu1195Asp
ENST00000406381.6:c.3495G>T	ENSP00000385185.2:p.Glu1165Asp
ENST00000445658.6:c.2757G>T	ENSP00000404047.2:p.Glu919Asp
ENST00000541774.5:c.3540G>T	ENSP00000446466.1:p.Glu1180Asp
ENST00000578373.5:c.*3375G>T	ENSP00000463427.1:n.*3375G>T
ENST00000584450.5:c.*164G>T	ENSP00000463714.1:n.*164G>T
ENST00000584601.5:c.3495G>T	ENSP00000462438.1:p.Glu1165Asp
NM_001005862.2:c.3495G>T , LRG_724t1:c.3495G>T	NP_001005862.1:p.Glu1165Asp
NM_001289936.1:c.3540G>T , LRG_724t4:c.3540G>T	NP_001276865.1:p.Glu1180Asp
NM_001289937.1:c.*164G>T	NP_001276866.1:n.*164G>T
NM_004448.3:c.3585G>T , LRG_724t2:c.3585G>T	NP_004439.2:p.Glu1195Asp
NR_110535.1:n.3909G>T
XM_024450641.1:c.3723G>T	XP_024306409.1:p.Glu1241Asp
XM_024450642.1:c.3678G>T	XP_024306410.1:p.Glu1226Asp
XM_024450643.1:c.3633G>T	XP_024306411.1:p.Glu1211Asp
NM_001005862.3:c.3495G>T	NP_001005862.1:p.Glu1165Asp
NM_001289936.2:c.3540G>T	NP_001276865.1:p.Glu1180Asp
NM_001289937.2:c.*164G>T	NP_001276866.1:n.*164G>T
NM_001382782.1:c.3495G>T	NP_001369711.1:p.Glu1165Asp
NM_001382783.1:c.3495G>T	NP_001369712.1:p.Glu1165Asp
NM_001382784.1:c.3702G>T	NP_001369713.1:p.Glu1234Asp
NM_001382785.1:c.3687G>T	NP_001369714.1:p.Glu1229Asp
NM_001382786.1:c.3666G>T	NP_001369715.1:p.Glu1222Asp
NM_001382787.1:c.3660G>T	NP_001369716.1:p.Glu1220Asp
NM_001382788.1:c.3615G>T	NP_001369717.1:p.Glu1205Asp
NM_001382789.1:c.3606G>T	NP_001369718.1:p.Glu1202Asp
NM_001382790.1:c.3582G>T	NP_001369719.1:p.Glu1194Asp
NM_001382791.1:c.3576G>T	NP_001369720.1:p.Glu1192Asp
NM_001382792.1:c.3549G>T	NP_001369721.1:p.Glu1183Asp
NM_001382793.1:c.3543G>T	NP_001369722.1:p.Glu1181Asp
NM_001382794.1:c.3543G>T	NP_001369723.1:p.Glu1181Asp
NM_001382795.1:c.3537G>T	NP_001369724.1:p.Glu1179Asp
NM_001382796.1:c.3498G>T	NP_001369725.1:p.Glu1166Asp
NM_001382797.1:c.3486G>T	NP_001369726.1:p.Glu1162Asp
NM_001382798.1:c.3429G>T	NP_001369727.1:p.Glu1143Asp
NM_001382799.1:c.3405G>T	NP_001369728.1:p.Glu1135Asp
NM_001382800.1:c.3399G>T	NP_001369729.1:p.Glu1133Asp
NM_001382801.1:c.3381G>T	NP_001369730.1:p.Glu1127Asp
NM_001382802.1:c.3327G>T	NP_001369731.1:p.Glu1109Asp
NM_001382803.1:c.*164G>T	NP_001369732.1:n.*164G>T
NM_001382804.1:c.2757G>T	NP_001369733.1:p.Glu919Asp
NM_001382805.1:c.2634G>T	NP_001369734.1:p.Glu878Asp
NM_001382806.1:c.2547G>T	NP_001369735.1:p.Glu849Asp
NM_004448.4:c.3585G>T MANE Select	NP_004439.2:p.Glu1195Asp
NR_110535.2:n.3823G>T