Canonical Allele Identifier: CA399312925

Gene: ERBB2

Linked Data

• dbSNP Id: rs1429281392
• gnomAD v4: 17-39727740-G-A
• MyVariant Identifiers: chr17:g.37883993G>A (hg19) ; chr17:g.39727740G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727740G>A , CM000679.2:g.39727740G>A	GRCh38
NC_000017.10:g.37883993G>A , CM000679.1:g.37883993G>A	GRCh37
NC_000017.9:g.35137519G>A	NCBI36
NG_007503.1:g.44601G>A , LRG_724:g.44601G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3464G>A MANE Select	ENSP00000269571.4:p.Gly1155Asp
ENST00000269571.9:c.3464G>A	ENSP00000269571.4:p.Gly1155Asp
ENST00000406381.6:c.3374G>A	ENSP00000385185.2:p.Gly1125Asp
ENST00000445658.6:c.2636G>A	ENSP00000404047.2:p.Gly879Asp
ENST00000541774.5:c.3419G>A	ENSP00000446466.1:p.Gly1140Asp
ENST00000578373.5:c.*3254G>A	ENSP00000463427.1:n.*3254G>A
ENST00000584450.5:c.*43G>A	ENSP00000463714.1:n.*43G>A
ENST00000584601.5:c.3374G>A	ENSP00000462438.1:p.Gly1125Asp
NM_001005862.2:c.3374G>A , LRG_724t1:c.3374G>A	NP_001005862.1:p.Gly1125Asp
NM_001289936.1:c.3419G>A , LRG_724t4:c.3419G>A	NP_001276865.1:p.Gly1140Asp
NM_001289937.1:c.*43G>A	NP_001276866.1:n.*43G>A
NM_004448.3:c.3464G>A , LRG_724t2:c.3464G>A	NP_004439.2:p.Gly1155Asp
NR_110535.1:n.3788G>A
XM_024450641.1:c.3602G>A	XP_024306409.1:p.Gly1201Asp
XM_024450642.1:c.3557G>A	XP_024306410.1:p.Gly1186Asp
XM_024450643.1:c.3512G>A	XP_024306411.1:p.Gly1171Asp
NM_001005862.3:c.3374G>A	NP_001005862.1:p.Gly1125Asp
NM_001289936.2:c.3419G>A	NP_001276865.1:p.Gly1140Asp
NM_001289937.2:c.*43G>A	NP_001276866.1:n.*43G>A
NM_001382782.1:c.3374G>A	NP_001369711.1:p.Gly1125Asp
NM_001382783.1:c.3374G>A	NP_001369712.1:p.Gly1125Asp
NM_001382784.1:c.3581G>A	NP_001369713.1:p.Gly1194Asp
NM_001382785.1:c.3566G>A	NP_001369714.1:p.Gly1189Asp
NM_001382786.1:c.3545G>A	NP_001369715.1:p.Gly1182Asp
NM_001382787.1:c.3539G>A	NP_001369716.1:p.Gly1180Asp
NM_001382788.1:c.3494G>A	NP_001369717.1:p.Gly1165Asp
NM_001382789.1:c.3485G>A	NP_001369718.1:p.Gly1162Asp
NM_001382790.1:c.3461G>A	NP_001369719.1:p.Gly1154Asp
NM_001382791.1:c.3455G>A	NP_001369720.1:p.Gly1152Asp
NM_001382792.1:c.3428G>A	NP_001369721.1:p.Gly1143Asp
NM_001382793.1:c.3422G>A	NP_001369722.1:p.Gly1141Asp
NM_001382794.1:c.3422G>A	NP_001369723.1:p.Gly1141Asp
NM_001382795.1:c.3416G>A	NP_001369724.1:p.Gly1139Asp
NM_001382796.1:c.3377G>A	NP_001369725.1:p.Gly1126Asp
NM_001382797.1:c.3365G>A	NP_001369726.1:p.Gly1122Asp
NM_001382798.1:c.3308G>A	NP_001369727.1:p.Gly1103Asp
NM_001382799.1:c.3284G>A	NP_001369728.1:p.Gly1095Asp
NM_001382800.1:c.3278G>A	NP_001369729.1:p.Gly1093Asp
NM_001382801.1:c.3260G>A	NP_001369730.1:p.Gly1087Asp
NM_001382802.1:c.3206G>A	NP_001369731.1:p.Gly1069Asp
NM_001382803.1:c.*43G>A	NP_001369732.1:n.*43G>A
NM_001382804.1:c.2636G>A	NP_001369733.1:p.Gly879Asp
NM_001382805.1:c.2513G>A	NP_001369734.1:p.Gly838Asp
NM_001382806.1:c.2426G>A	NP_001369735.1:p.Gly809Asp
NM_004448.4:c.3464G>A MANE Select	NP_004439.2:p.Gly1155Asp
NR_110535.2:n.3702G>A