Canonical Allele Identifier: CA399313672

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884101T>G (hg19) ; chr17:g.39727848T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727848T>G , CM000679.2:g.39727848T>G	GRCh38
NC_000017.10:g.37884101T>G , CM000679.1:g.37884101T>G	GRCh37
NC_000017.9:g.35137627T>G	NCBI36
NG_007503.1:g.44709T>G , LRG_724:g.44709T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3572T>G MANE Select	ENSP00000269571.4:p.Val1191Gly
ENST00000269571.9:c.3572T>G	ENSP00000269571.4:p.Val1191Gly
ENST00000406381.6:c.3482T>G	ENSP00000385185.2:p.Val1161Gly
ENST00000445658.6:c.2744T>G	ENSP00000404047.2:p.Val915Gly
ENST00000541774.5:c.3527T>G	ENSP00000446466.1:p.Val1176Gly
ENST00000578373.5:c.*3362T>G	ENSP00000463427.1:n.*3362T>G
ENST00000584450.5:c.*151T>G	ENSP00000463714.1:n.*151T>G
ENST00000584601.5:c.3482T>G	ENSP00000462438.1:p.Val1161Gly
NM_001005862.2:c.3482T>G , LRG_724t1:c.3482T>G	NP_001005862.1:p.Val1161Gly
NM_001289936.1:c.3527T>G , LRG_724t4:c.3527T>G	NP_001276865.1:p.Val1176Gly
NM_001289937.1:c.*151T>G	NP_001276866.1:n.*151T>G
NM_004448.3:c.3572T>G , LRG_724t2:c.3572T>G	NP_004439.2:p.Val1191Gly
NR_110535.1:n.3896T>G
XM_024450641.1:c.3710T>G	XP_024306409.1:p.Val1237Gly
XM_024450642.1:c.3665T>G	XP_024306410.1:p.Val1222Gly
XM_024450643.1:c.3620T>G	XP_024306411.1:p.Val1207Gly
NM_001005862.3:c.3482T>G	NP_001005862.1:p.Val1161Gly
NM_001289936.2:c.3527T>G	NP_001276865.1:p.Val1176Gly
NM_001289937.2:c.*151T>G	NP_001276866.1:n.*151T>G
NM_001382782.1:c.3482T>G	NP_001369711.1:p.Val1161Gly
NM_001382783.1:c.3482T>G	NP_001369712.1:p.Val1161Gly
NM_001382784.1:c.3689T>G	NP_001369713.1:p.Val1230Gly
NM_001382785.1:c.3674T>G	NP_001369714.1:p.Val1225Gly
NM_001382786.1:c.3653T>G	NP_001369715.1:p.Val1218Gly
NM_001382787.1:c.3647T>G	NP_001369716.1:p.Val1216Gly
NM_001382788.1:c.3602T>G	NP_001369717.1:p.Val1201Gly
NM_001382789.1:c.3593T>G	NP_001369718.1:p.Val1198Gly
NM_001382790.1:c.3569T>G	NP_001369719.1:p.Val1190Gly
NM_001382791.1:c.3563T>G	NP_001369720.1:p.Val1188Gly
NM_001382792.1:c.3536T>G	NP_001369721.1:p.Val1179Gly
NM_001382793.1:c.3530T>G	NP_001369722.1:p.Val1177Gly
NM_001382794.1:c.3530T>G	NP_001369723.1:p.Val1177Gly
NM_001382795.1:c.3524T>G	NP_001369724.1:p.Val1175Gly
NM_001382796.1:c.3485T>G	NP_001369725.1:p.Val1162Gly
NM_001382797.1:c.3473T>G	NP_001369726.1:p.Val1158Gly
NM_001382798.1:c.3416T>G	NP_001369727.1:p.Val1139Gly
NM_001382799.1:c.3392T>G	NP_001369728.1:p.Val1131Gly
NM_001382800.1:c.3386T>G	NP_001369729.1:p.Val1129Gly
NM_001382801.1:c.3368T>G	NP_001369730.1:p.Val1123Gly
NM_001382802.1:c.3314T>G	NP_001369731.1:p.Val1105Gly
NM_001382803.1:c.*151T>G	NP_001369732.1:n.*151T>G
NM_001382804.1:c.2744T>G	NP_001369733.1:p.Val915Gly
NM_001382805.1:c.2621T>G	NP_001369734.1:p.Val874Gly
NM_001382806.1:c.2534T>G	NP_001369735.1:p.Val845Gly
NM_004448.4:c.3572T>G MANE Select	NP_004439.2:p.Val1191Gly
NR_110535.2:n.3810T>G