Canonical Allele Identifier: CA399312639

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143254154
• MyVariant Identifiers: chr17:g.37883741T>G (hg19) ; chr17:g.39727488T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727488T>G , CM000679.2:g.39727488T>G	GRCh38
NC_000017.10:g.37883741T>G , CM000679.1:g.37883741T>G	GRCh37
NC_000017.9:g.35137267T>G	NCBI36
NG_007503.1:g.44349T>G , LRG_724:g.44349T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3353T>G MANE Select	ENSP00000269571.4:p.Val1118Gly
ENST00000269571.9:c.3353T>G	ENSP00000269571.4:p.Val1118Gly
ENST00000406381.6:c.3263T>G	ENSP00000385185.2:p.Val1088Gly
ENST00000445658.6:c.2525T>G	ENSP00000404047.2:p.Val842Gly
ENST00000541774.5:c.3308T>G	ENSP00000446466.1:p.Val1103Gly
ENST00000578373.5:c.*3143T>G	ENSP00000463427.1:n.*3143T>G
ENST00000584450.5:c.3160-201T>G	ENSP00000463714.1:n.3160-201T>G
ENST00000584601.5:c.3263T>G	ENSP00000462438.1:p.Val1088Gly
NM_001005862.2:c.3263T>G , LRG_724t1:c.3263T>G	NP_001005862.1:p.Val1088Gly
NM_001289936.1:c.3308T>G , LRG_724t4:c.3308T>G	NP_001276865.1:p.Val1103Gly
NM_001289937.1:c.3160-201T>G	NP_001276866.1:n.3160-201T>G
NM_004448.3:c.3353T>G , LRG_724t2:c.3353T>G	NP_004439.2:p.Val1118Gly
NR_110535.1:n.3677T>G
XM_024450641.1:c.3491T>G	XP_024306409.1:p.Val1164Gly
XM_024450642.1:c.3446T>G	XP_024306410.1:p.Val1149Gly
XM_024450643.1:c.3401T>G	XP_024306411.1:p.Val1134Gly
NM_001005862.3:c.3263T>G	NP_001005862.1:p.Val1088Gly
NM_001289936.2:c.3308T>G	NP_001276865.1:p.Val1103Gly
NM_001289937.2:c.3160-201T>G	NP_001276866.1:n.3160-201T>G
NM_001382782.1:c.3263T>G	NP_001369711.1:p.Val1088Gly
NM_001382783.1:c.3263T>G	NP_001369712.1:p.Val1088Gly
NM_001382784.1:c.3470T>G	NP_001369713.1:p.Val1157Gly
NM_001382785.1:c.3455T>G	NP_001369714.1:p.Val1152Gly
NM_001382786.1:c.3434T>G	NP_001369715.1:p.Val1145Gly
NM_001382787.1:c.3428T>G	NP_001369716.1:p.Val1143Gly
NM_001382788.1:c.3383T>G	NP_001369717.1:p.Val1128Gly
NM_001382789.1:c.3374T>G	NP_001369718.1:p.Val1125Gly
NM_001382790.1:c.3350T>G	NP_001369719.1:p.Val1117Gly
NM_001382791.1:c.3344T>G	NP_001369720.1:p.Val1115Gly
NM_001382792.1:c.3317T>G	NP_001369721.1:p.Val1106Gly
NM_001382793.1:c.3311T>G	NP_001369722.1:p.Val1104Gly
NM_001382794.1:c.3311T>G	NP_001369723.1:p.Val1104Gly
NM_001382795.1:c.3305T>G	NP_001369724.1:p.Val1102Gly
NM_001382796.1:c.3266T>G	NP_001369725.1:p.Val1089Gly
NM_001382797.1:c.3254T>G	NP_001369726.1:p.Val1085Gly
NM_001382798.1:c.3197T>G	NP_001369727.1:p.Val1066Gly
NM_001382799.1:c.3173T>G	NP_001369728.1:p.Val1058Gly
NM_001382800.1:c.3167T>G	NP_001369729.1:p.Val1056Gly
NM_001382801.1:c.3149T>G	NP_001369730.1:p.Val1050Gly
NM_001382802.1:c.3095T>G	NP_001369731.1:p.Val1032Gly
NM_001382803.1:c.3118-201T>G	NP_001369732.1:n.3118-201T>G
NM_001382804.1:c.2525T>G	NP_001369733.1:p.Val842Gly
NM_001382805.1:c.2402T>G	NP_001369734.1:p.Val801Gly
NM_001382806.1:c.2315T>G	NP_001369735.1:p.Val772Gly
NM_004448.4:c.3353T>G MANE Select	NP_004439.2:p.Val1118Gly
NR_110535.2:n.3591T>G