Canonical Allele Identifier: CA399313395

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143299089
• MyVariant Identifiers: chr17:g.37884064G>T (hg19) ; chr17:g.39727811G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727811G>T , CM000679.2:g.39727811G>T	GRCh38
NC_000017.10:g.37884064G>T , CM000679.1:g.37884064G>T	GRCh37
NC_000017.9:g.35137590G>T	NCBI36
NG_007503.1:g.44672G>T , LRG_724:g.44672G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3535G>T MANE Select	ENSP00000269571.4:p.Gly1179Trp
ENST00000269571.9:c.3535G>T	ENSP00000269571.4:p.Gly1179Trp
ENST00000406381.6:c.3445G>T	ENSP00000385185.2:p.Gly1149Trp
ENST00000445658.6:c.2707G>T	ENSP00000404047.2:p.Gly903Trp
ENST00000541774.5:c.3490G>T	ENSP00000446466.1:p.Gly1164Trp
ENST00000578373.5:c.*3325G>T	ENSP00000463427.1:n.*3325G>T
ENST00000584450.5:c.*114G>T	ENSP00000463714.1:n.*114G>T
ENST00000584601.5:c.3445G>T	ENSP00000462438.1:p.Gly1149Trp
NM_001005862.2:c.3445G>T , LRG_724t1:c.3445G>T	NP_001005862.1:p.Gly1149Trp
NM_001289936.1:c.3490G>T , LRG_724t4:c.3490G>T	NP_001276865.1:p.Gly1164Trp
NM_001289937.1:c.*114G>T	NP_001276866.1:n.*114G>T
NM_004448.3:c.3535G>T , LRG_724t2:c.3535G>T	NP_004439.2:p.Gly1179Trp
NR_110535.1:n.3859G>T
XM_024450641.1:c.3673G>T	XP_024306409.1:p.Gly1225Trp
XM_024450642.1:c.3628G>T	XP_024306410.1:p.Gly1210Trp
XM_024450643.1:c.3583G>T	XP_024306411.1:p.Gly1195Trp
NM_001005862.3:c.3445G>T	NP_001005862.1:p.Gly1149Trp
NM_001289936.2:c.3490G>T	NP_001276865.1:p.Gly1164Trp
NM_001289937.2:c.*114G>T	NP_001276866.1:n.*114G>T
NM_001382782.1:c.3445G>T	NP_001369711.1:p.Gly1149Trp
NM_001382783.1:c.3445G>T	NP_001369712.1:p.Gly1149Trp
NM_001382784.1:c.3652G>T	NP_001369713.1:p.Gly1218Trp
NM_001382785.1:c.3637G>T	NP_001369714.1:p.Gly1213Trp
NM_001382786.1:c.3616G>T	NP_001369715.1:p.Gly1206Trp
NM_001382787.1:c.3610G>T	NP_001369716.1:p.Gly1204Trp
NM_001382788.1:c.3565G>T	NP_001369717.1:p.Gly1189Trp
NM_001382789.1:c.3556G>T	NP_001369718.1:p.Gly1186Trp
NM_001382790.1:c.3532G>T	NP_001369719.1:p.Gly1178Trp
NM_001382791.1:c.3526G>T	NP_001369720.1:p.Gly1176Trp
NM_001382792.1:c.3499G>T	NP_001369721.1:p.Gly1167Trp
NM_001382793.1:c.3493G>T	NP_001369722.1:p.Gly1165Trp
NM_001382794.1:c.3493G>T	NP_001369723.1:p.Gly1165Trp
NM_001382795.1:c.3487G>T	NP_001369724.1:p.Gly1163Trp
NM_001382796.1:c.3448G>T	NP_001369725.1:p.Gly1150Trp
NM_001382797.1:c.3436G>T	NP_001369726.1:p.Gly1146Trp
NM_001382798.1:c.3379G>T	NP_001369727.1:p.Gly1127Trp
NM_001382799.1:c.3355G>T	NP_001369728.1:p.Gly1119Trp
NM_001382800.1:c.3349G>T	NP_001369729.1:p.Gly1117Trp
NM_001382801.1:c.3331G>T	NP_001369730.1:p.Gly1111Trp
NM_001382802.1:c.3277G>T	NP_001369731.1:p.Gly1093Trp
NM_001382803.1:c.*114G>T	NP_001369732.1:n.*114G>T
NM_001382804.1:c.2707G>T	NP_001369733.1:p.Gly903Trp
NM_001382805.1:c.2584G>T	NP_001369734.1:p.Gly862Trp
NM_001382806.1:c.2497G>T	NP_001369735.1:p.Gly833Trp
NM_004448.4:c.3535G>T MANE Select	NP_004439.2:p.Gly1179Trp
NR_110535.2:n.3773G>T