Canonical Allele Identifier: CA399313627

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059865909
• gnomAD v4: 17-39727842-G-A
• MyVariant Identifiers: chr17:g.37884095G>A (hg19) ; chr17:g.39727842G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727842G>A , CM000679.2:g.39727842G>A	GRCh38
NC_000017.10:g.37884095G>A , CM000679.1:g.37884095G>A	GRCh37
NC_000017.9:g.35137621G>A	NCBI36
NG_007503.1:g.44703G>A , LRG_724:g.44703G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3566G>A MANE Select	ENSP00000269571.4:p.Gly1189Asp
ENST00000269571.9:c.3566G>A	ENSP00000269571.4:p.Gly1189Asp
ENST00000406381.6:c.3476G>A	ENSP00000385185.2:p.Gly1159Asp
ENST00000445658.6:c.2738G>A	ENSP00000404047.2:p.Gly913Asp
ENST00000541774.5:c.3521G>A	ENSP00000446466.1:p.Gly1174Asp
ENST00000578373.5:c.*3356G>A	ENSP00000463427.1:n.*3356G>A
ENST00000584450.5:c.*145G>A	ENSP00000463714.1:n.*145G>A
ENST00000584601.5:c.3476G>A	ENSP00000462438.1:p.Gly1159Asp
NM_001005862.2:c.3476G>A , LRG_724t1:c.3476G>A	NP_001005862.1:p.Gly1159Asp
NM_001289936.1:c.3521G>A , LRG_724t4:c.3521G>A	NP_001276865.1:p.Gly1174Asp
NM_001289937.1:c.*145G>A	NP_001276866.1:n.*145G>A
NM_004448.3:c.3566G>A , LRG_724t2:c.3566G>A	NP_004439.2:p.Gly1189Asp
NR_110535.1:n.3890G>A
XM_024450641.1:c.3704G>A	XP_024306409.1:p.Gly1235Asp
XM_024450642.1:c.3659G>A	XP_024306410.1:p.Gly1220Asp
XM_024450643.1:c.3614G>A	XP_024306411.1:p.Gly1205Asp
NM_001005862.3:c.3476G>A	NP_001005862.1:p.Gly1159Asp
NM_001289936.2:c.3521G>A	NP_001276865.1:p.Gly1174Asp
NM_001289937.2:c.*145G>A	NP_001276866.1:n.*145G>A
NM_001382782.1:c.3476G>A	NP_001369711.1:p.Gly1159Asp
NM_001382783.1:c.3476G>A	NP_001369712.1:p.Gly1159Asp
NM_001382784.1:c.3683G>A	NP_001369713.1:p.Gly1228Asp
NM_001382785.1:c.3668G>A	NP_001369714.1:p.Gly1223Asp
NM_001382786.1:c.3647G>A	NP_001369715.1:p.Gly1216Asp
NM_001382787.1:c.3641G>A	NP_001369716.1:p.Gly1214Asp
NM_001382788.1:c.3596G>A	NP_001369717.1:p.Gly1199Asp
NM_001382789.1:c.3587G>A	NP_001369718.1:p.Gly1196Asp
NM_001382790.1:c.3563G>A	NP_001369719.1:p.Gly1188Asp
NM_001382791.1:c.3557G>A	NP_001369720.1:p.Gly1186Asp
NM_001382792.1:c.3530G>A	NP_001369721.1:p.Gly1177Asp
NM_001382793.1:c.3524G>A	NP_001369722.1:p.Gly1175Asp
NM_001382794.1:c.3524G>A	NP_001369723.1:p.Gly1175Asp
NM_001382795.1:c.3518G>A	NP_001369724.1:p.Gly1173Asp
NM_001382796.1:c.3479G>A	NP_001369725.1:p.Gly1160Asp
NM_001382797.1:c.3467G>A	NP_001369726.1:p.Gly1156Asp
NM_001382798.1:c.3410G>A	NP_001369727.1:p.Gly1137Asp
NM_001382799.1:c.3386G>A	NP_001369728.1:p.Gly1129Asp
NM_001382800.1:c.3380G>A	NP_001369729.1:p.Gly1127Asp
NM_001382801.1:c.3362G>A	NP_001369730.1:p.Gly1121Asp
NM_001382802.1:c.3308G>A	NP_001369731.1:p.Gly1103Asp
NM_001382803.1:c.*145G>A	NP_001369732.1:n.*145G>A
NM_001382804.1:c.2738G>A	NP_001369733.1:p.Gly913Asp
NM_001382805.1:c.2615G>A	NP_001369734.1:p.Gly872Asp
NM_001382806.1:c.2528G>A	NP_001369735.1:p.Gly843Asp
NM_004448.4:c.3566G>A MANE Select	NP_004439.2:p.Gly1189Asp
NR_110535.2:n.3804G>A