Canonical Allele Identifier: CA399313623

Gene: ERBB2

Linked Data

• dbSNP Id: rs926640472
• gnomAD v4: 17-39727841-G-T
• MyVariant Identifiers: chr17:g.37884094G>T (hg19) ; chr17:g.39727841G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727841G>T , CM000679.2:g.39727841G>T	GRCh38
NC_000017.10:g.37884094G>T , CM000679.1:g.37884094G>T	GRCh37
NC_000017.9:g.35137620G>T	NCBI36
NG_007503.1:g.44702G>T , LRG_724:g.44702G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3565G>T MANE Select	ENSP00000269571.4:p.Gly1189Cys
ENST00000269571.9:c.3565G>T	ENSP00000269571.4:p.Gly1189Cys
ENST00000406381.6:c.3475G>T	ENSP00000385185.2:p.Gly1159Cys
ENST00000445658.6:c.2737G>T	ENSP00000404047.2:p.Gly913Cys
ENST00000541774.5:c.3520G>T	ENSP00000446466.1:p.Gly1174Cys
ENST00000578373.5:c.*3355G>T	ENSP00000463427.1:n.*3355G>T
ENST00000584450.5:c.*144G>T	ENSP00000463714.1:n.*144G>T
ENST00000584601.5:c.3475G>T	ENSP00000462438.1:p.Gly1159Cys
NM_001005862.2:c.3475G>T , LRG_724t1:c.3475G>T	NP_001005862.1:p.Gly1159Cys
NM_001289936.1:c.3520G>T , LRG_724t4:c.3520G>T	NP_001276865.1:p.Gly1174Cys
NM_001289937.1:c.*144G>T	NP_001276866.1:n.*144G>T
NM_004448.3:c.3565G>T , LRG_724t2:c.3565G>T	NP_004439.2:p.Gly1189Cys
NR_110535.1:n.3889G>T
XM_024450641.1:c.3703G>T	XP_024306409.1:p.Gly1235Cys
XM_024450642.1:c.3658G>T	XP_024306410.1:p.Gly1220Cys
XM_024450643.1:c.3613G>T	XP_024306411.1:p.Gly1205Cys
NM_001005862.3:c.3475G>T	NP_001005862.1:p.Gly1159Cys
NM_001289936.2:c.3520G>T	NP_001276865.1:p.Gly1174Cys
NM_001289937.2:c.*144G>T	NP_001276866.1:n.*144G>T
NM_001382782.1:c.3475G>T	NP_001369711.1:p.Gly1159Cys
NM_001382783.1:c.3475G>T	NP_001369712.1:p.Gly1159Cys
NM_001382784.1:c.3682G>T	NP_001369713.1:p.Gly1228Cys
NM_001382785.1:c.3667G>T	NP_001369714.1:p.Gly1223Cys
NM_001382786.1:c.3646G>T	NP_001369715.1:p.Gly1216Cys
NM_001382787.1:c.3640G>T	NP_001369716.1:p.Gly1214Cys
NM_001382788.1:c.3595G>T	NP_001369717.1:p.Gly1199Cys
NM_001382789.1:c.3586G>T	NP_001369718.1:p.Gly1196Cys
NM_001382790.1:c.3562G>T	NP_001369719.1:p.Gly1188Cys
NM_001382791.1:c.3556G>T	NP_001369720.1:p.Gly1186Cys
NM_001382792.1:c.3529G>T	NP_001369721.1:p.Gly1177Cys
NM_001382793.1:c.3523G>T	NP_001369722.1:p.Gly1175Cys
NM_001382794.1:c.3523G>T	NP_001369723.1:p.Gly1175Cys
NM_001382795.1:c.3517G>T	NP_001369724.1:p.Gly1173Cys
NM_001382796.1:c.3478G>T	NP_001369725.1:p.Gly1160Cys
NM_001382797.1:c.3466G>T	NP_001369726.1:p.Gly1156Cys
NM_001382798.1:c.3409G>T	NP_001369727.1:p.Gly1137Cys
NM_001382799.1:c.3385G>T	NP_001369728.1:p.Gly1129Cys
NM_001382800.1:c.3379G>T	NP_001369729.1:p.Gly1127Cys
NM_001382801.1:c.3361G>T	NP_001369730.1:p.Gly1121Cys
NM_001382802.1:c.3307G>T	NP_001369731.1:p.Gly1103Cys
NM_001382803.1:c.*144G>T	NP_001369732.1:n.*144G>T
NM_001382804.1:c.2737G>T	NP_001369733.1:p.Gly913Cys
NM_001382805.1:c.2614G>T	NP_001369734.1:p.Gly872Cys
NM_001382806.1:c.2527G>T	NP_001369735.1:p.Gly843Cys
NM_004448.4:c.3565G>T MANE Select	NP_004439.2:p.Gly1189Cys
NR_110535.2:n.3803G>T