Canonical Allele Identifier: CA399312927

Gene: ERBB2

Linked Data

• dbSNP Id: rs1429281392
• MyVariant Identifiers: chr17:g.37883993G>C (hg19) ; chr17:g.39727740G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3464G>C MANE Select	ENSP00000269571.4:p.Gly1155Ala
ENST00000269571.9:c.3464G>C	ENSP00000269571.4:p.Gly1155Ala
ENST00000406381.6:c.3374G>C	ENSP00000385185.2:p.Gly1125Ala
ENST00000445658.6:c.2636G>C	ENSP00000404047.2:p.Gly879Ala
ENST00000541774.5:c.3419G>C	ENSP00000446466.1:p.Gly1140Ala
ENST00000578373.5:c.*3254G>C	ENSP00000463427.1:n.*3254G>C
ENST00000584450.5:c.*43G>C	ENSP00000463714.1:n.*43G>C
ENST00000584601.5:c.3374G>C	ENSP00000462438.1:p.Gly1125Ala
NM_001005862.2:c.3374G>C , LRG_724t1:c.3374G>C	NP_001005862.1:p.Gly1125Ala
NM_001289936.1:c.3419G>C , LRG_724t4:c.3419G>C	NP_001276865.1:p.Gly1140Ala
NM_001289937.1:c.*43G>C	NP_001276866.1:n.*43G>C
NM_004448.3:c.3464G>C , LRG_724t2:c.3464G>C	NP_004439.2:p.Gly1155Ala
NR_110535.1:n.3788G>C
XM_024450641.1:c.3602G>C	XP_024306409.1:p.Gly1201Ala
XM_024450642.1:c.3557G>C	XP_024306410.1:p.Gly1186Ala
XM_024450643.1:c.3512G>C	XP_024306411.1:p.Gly1171Ala
NM_001005862.3:c.3374G>C	NP_001005862.1:p.Gly1125Ala
NM_001289936.2:c.3419G>C	NP_001276865.1:p.Gly1140Ala
NM_001289937.2:c.*43G>C	NP_001276866.1:n.*43G>C
NM_001382782.1:c.3374G>C	NP_001369711.1:p.Gly1125Ala
NM_001382783.1:c.3374G>C	NP_001369712.1:p.Gly1125Ala
NM_001382784.1:c.3581G>C	NP_001369713.1:p.Gly1194Ala
NM_001382785.1:c.3566G>C	NP_001369714.1:p.Gly1189Ala
NM_001382786.1:c.3545G>C	NP_001369715.1:p.Gly1182Ala
NM_001382787.1:c.3539G>C	NP_001369716.1:p.Gly1180Ala
NM_001382788.1:c.3494G>C	NP_001369717.1:p.Gly1165Ala
NM_001382789.1:c.3485G>C	NP_001369718.1:p.Gly1162Ala
NM_001382790.1:c.3461G>C	NP_001369719.1:p.Gly1154Ala
NM_001382791.1:c.3455G>C	NP_001369720.1:p.Gly1152Ala
NM_001382792.1:c.3428G>C	NP_001369721.1:p.Gly1143Ala
NM_001382793.1:c.3422G>C	NP_001369722.1:p.Gly1141Ala
NM_001382794.1:c.3422G>C	NP_001369723.1:p.Gly1141Ala
NM_001382795.1:c.3416G>C	NP_001369724.1:p.Gly1139Ala
NM_001382796.1:c.3377G>C	NP_001369725.1:p.Gly1126Ala
NM_001382797.1:c.3365G>C	NP_001369726.1:p.Gly1122Ala
NM_001382798.1:c.3308G>C	NP_001369727.1:p.Gly1103Ala
NM_001382799.1:c.3284G>C	NP_001369728.1:p.Gly1095Ala
NM_001382800.1:c.3278G>C	NP_001369729.1:p.Gly1093Ala
NM_001382801.1:c.3260G>C	NP_001369730.1:p.Gly1087Ala
NM_001382802.1:c.3206G>C	NP_001369731.1:p.Gly1069Ala
NM_001382803.1:c.*43G>C	NP_001369732.1:n.*43G>C
NM_001382804.1:c.2636G>C	NP_001369733.1:p.Gly879Ala
NM_001382805.1:c.2513G>C	NP_001369734.1:p.Gly838Ala
NM_001382806.1:c.2426G>C	NP_001369735.1:p.Gly809Ala
NM_004448.4:c.3464G>C MANE Select	NP_004439.2:p.Gly1155Ala
NR_110535.2:n.3702G>C