Canonical Allele Identifier: CA399314487

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059872380
• gnomAD v3: 17-39727953-A-G
• gnomAD v4: 17-39727953-A-G
• MyVariant Identifiers: chr17:g.37884206A>G (hg19) ; chr17:g.39727953A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727953A>G , CM000679.2:g.39727953A>G	GRCh38
NC_000017.10:g.37884206A>G , CM000679.1:g.37884206A>G	GRCh37
NC_000017.9:g.35137732A>G	NCBI36
NG_007503.1:g.44814A>G , LRG_724:g.44814A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3677A>G MANE Select	ENSP00000269571.4:p.Asp1226Gly
ENST00000269571.9:c.3677A>G	ENSP00000269571.4:p.Asp1226Gly
ENST00000406381.6:c.3587A>G	ENSP00000385185.2:p.Asp1196Gly
ENST00000445658.6:c.2849A>G	ENSP00000404047.2:p.Asp950Gly
ENST00000541774.5:c.3632A>G	ENSP00000446466.1:p.Asp1211Gly
ENST00000578373.5:c.*3467A>G	ENSP00000463427.1:n.*3467A>G
ENST00000584450.5:c.*256A>G	ENSP00000463714.1:n.*256A>G
ENST00000584601.5:c.3587A>G	ENSP00000462438.1:p.Asp1196Gly
NM_001005862.2:c.3587A>G , LRG_724t1:c.3587A>G	NP_001005862.1:p.Asp1196Gly
NM_001289936.1:c.3632A>G , LRG_724t4:c.3632A>G	NP_001276865.1:p.Asp1211Gly
NM_001289937.1:c.*256A>G	NP_001276866.1:n.*256A>G
NM_004448.3:c.3677A>G , LRG_724t2:c.3677A>G	NP_004439.2:p.Asp1226Gly
NR_110535.1:n.4001A>G
XM_024450641.1:c.3815A>G	XP_024306409.1:p.Asp1272Gly
XM_024450642.1:c.3770A>G	XP_024306410.1:p.Asp1257Gly
XM_024450643.1:c.3725A>G	XP_024306411.1:p.Asp1242Gly
NM_001005862.3:c.3587A>G	NP_001005862.1:p.Asp1196Gly
NM_001289936.2:c.3632A>G	NP_001276865.1:p.Asp1211Gly
NM_001289937.2:c.*256A>G	NP_001276866.1:n.*256A>G
NM_001382782.1:c.3587A>G	NP_001369711.1:p.Asp1196Gly
NM_001382783.1:c.3587A>G	NP_001369712.1:p.Asp1196Gly
NM_001382784.1:c.3794A>G	NP_001369713.1:p.Asp1265Gly
NM_001382785.1:c.3779A>G	NP_001369714.1:p.Asp1260Gly
NM_001382786.1:c.3758A>G	NP_001369715.1:p.Asp1253Gly
NM_001382787.1:c.3752A>G	NP_001369716.1:p.Asp1251Gly
NM_001382788.1:c.3707A>G	NP_001369717.1:p.Asp1236Gly
NM_001382789.1:c.3698A>G	NP_001369718.1:p.Asp1233Gly
NM_001382790.1:c.3674A>G	NP_001369719.1:p.Asp1225Gly
NM_001382791.1:c.3668A>G	NP_001369720.1:p.Asp1223Gly
NM_001382792.1:c.3641A>G	NP_001369721.1:p.Asp1214Gly
NM_001382793.1:c.3635A>G	NP_001369722.1:p.Asp1212Gly
NM_001382794.1:c.3635A>G	NP_001369723.1:p.Asp1212Gly
NM_001382795.1:c.3629A>G	NP_001369724.1:p.Asp1210Gly
NM_001382796.1:c.3590A>G	NP_001369725.1:p.Asp1197Gly
NM_001382797.1:c.3578A>G	NP_001369726.1:p.Asp1193Gly
NM_001382798.1:c.3521A>G	NP_001369727.1:p.Asp1174Gly
NM_001382799.1:c.3497A>G	NP_001369728.1:p.Asp1166Gly
NM_001382800.1:c.3491A>G	NP_001369729.1:p.Asp1164Gly
NM_001382801.1:c.3473A>G	NP_001369730.1:p.Asp1158Gly
NM_001382802.1:c.3419A>G	NP_001369731.1:p.Asp1140Gly
NM_001382803.1:c.*256A>G	NP_001369732.1:n.*256A>G
NM_001382804.1:c.2849A>G	NP_001369733.1:p.Asp950Gly
NM_001382805.1:c.2726A>G	NP_001369734.1:p.Asp909Gly
NM_001382806.1:c.2639A>G	NP_001369735.1:p.Asp880Gly
NM_004448.4:c.3677A>G MANE Select	NP_004439.2:p.Asp1226Gly
NR_110535.2:n.3915A>G