Canonical Allele Identifier: CA399312729

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143256967
• gnomAD v4: 17-39727512-G-A
• MyVariant Identifiers: chr17:g.37883765G>A (hg19) ; chr17:g.39727512G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727512G>A , CM000679.2:g.39727512G>A	GRCh38
NC_000017.10:g.37883765G>A , CM000679.1:g.37883765G>A	GRCh37
NC_000017.9:g.35137291G>A	NCBI36
NG_007503.1:g.44373G>A , LRG_724:g.44373G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3377G>A MANE Select	ENSP00000269571.4:p.Gly1126Asp
ENST00000269571.9:c.3377G>A	ENSP00000269571.4:p.Gly1126Asp
ENST00000406381.6:c.3287G>A	ENSP00000385185.2:p.Gly1096Asp
ENST00000445658.6:c.2549G>A	ENSP00000404047.2:p.Gly850Asp
ENST00000541774.5:c.3332G>A	ENSP00000446466.1:p.Gly1111Asp
ENST00000578373.5:c.*3167G>A	ENSP00000463427.1:n.*3167G>A
ENST00000584450.5:c.3160-177G>A	ENSP00000463714.1:n.3160-177G>A
ENST00000584601.5:c.3287G>A	ENSP00000462438.1:p.Gly1096Asp
NM_001005862.2:c.3287G>A , LRG_724t1:c.3287G>A	NP_001005862.1:p.Gly1096Asp
NM_001289936.1:c.3332G>A , LRG_724t4:c.3332G>A	NP_001276865.1:p.Gly1111Asp
NM_001289937.1:c.3160-177G>A	NP_001276866.1:n.3160-177G>A
NM_004448.3:c.3377G>A , LRG_724t2:c.3377G>A	NP_004439.2:p.Gly1126Asp
NR_110535.1:n.3701G>A
XM_024450641.1:c.3515G>A	XP_024306409.1:p.Gly1172Asp
XM_024450642.1:c.3470G>A	XP_024306410.1:p.Gly1157Asp
XM_024450643.1:c.3425G>A	XP_024306411.1:p.Gly1142Asp
NM_001005862.3:c.3287G>A	NP_001005862.1:p.Gly1096Asp
NM_001289936.2:c.3332G>A	NP_001276865.1:p.Gly1111Asp
NM_001289937.2:c.3160-177G>A	NP_001276866.1:n.3160-177G>A
NM_001382782.1:c.3287G>A	NP_001369711.1:p.Gly1096Asp
NM_001382783.1:c.3287G>A	NP_001369712.1:p.Gly1096Asp
NM_001382784.1:c.3494G>A	NP_001369713.1:p.Gly1165Asp
NM_001382785.1:c.3479G>A	NP_001369714.1:p.Gly1160Asp
NM_001382786.1:c.3458G>A	NP_001369715.1:p.Gly1153Asp
NM_001382787.1:c.3452G>A	NP_001369716.1:p.Gly1151Asp
NM_001382788.1:c.3407G>A	NP_001369717.1:p.Gly1136Asp
NM_001382789.1:c.3398G>A	NP_001369718.1:p.Gly1133Asp
NM_001382790.1:c.3374G>A	NP_001369719.1:p.Gly1125Asp
NM_001382791.1:c.3368G>A	NP_001369720.1:p.Gly1123Asp
NM_001382792.1:c.3341G>A	NP_001369721.1:p.Gly1114Asp
NM_001382793.1:c.3335G>A	NP_001369722.1:p.Gly1112Asp
NM_001382794.1:c.3335G>A	NP_001369723.1:p.Gly1112Asp
NM_001382795.1:c.3329G>A	NP_001369724.1:p.Gly1110Asp
NM_001382796.1:c.3290G>A	NP_001369725.1:p.Gly1097Asp
NM_001382797.1:c.3278G>A	NP_001369726.1:p.Gly1093Asp
NM_001382798.1:c.3221G>A	NP_001369727.1:p.Gly1074Asp
NM_001382799.1:c.3197G>A	NP_001369728.1:p.Gly1066Asp
NM_001382800.1:c.3191G>A	NP_001369729.1:p.Gly1064Asp
NM_001382801.1:c.3173G>A	NP_001369730.1:p.Gly1058Asp
NM_001382802.1:c.3119G>A	NP_001369731.1:p.Gly1040Asp
NM_001382803.1:c.3118-177G>A	NP_001369732.1:n.3118-177G>A
NM_001382804.1:c.2549G>A	NP_001369733.1:p.Gly850Asp
NM_001382805.1:c.2426G>A	NP_001369734.1:p.Gly809Asp
NM_001382806.1:c.2339G>A	NP_001369735.1:p.Gly780Asp
NM_004448.4:c.3377G>A MANE Select	NP_004439.2:p.Gly1126Asp
NR_110535.2:n.3615G>A