Canonical Allele Identifier: CA399312530

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143251251
• MyVariant Identifiers: chr17:g.37883716C>G (hg19) ; chr17:g.39727463C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727463C>G , CM000679.2:g.39727463C>G	GRCh38
NC_000017.10:g.37883716C>G , CM000679.1:g.37883716C>G	GRCh37
NC_000017.9:g.35137242C>G	NCBI36
NG_007503.1:g.44324C>G , LRG_724:g.44324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3328C>G MANE Select	ENSP00000269571.4:p.Gln1110Glu
ENST00000269571.9:c.3328C>G	ENSP00000269571.4:p.Gln1110Glu
ENST00000406381.6:c.3238C>G	ENSP00000385185.2:p.Gln1080Glu
ENST00000445658.6:c.2500C>G	ENSP00000404047.2:p.Gln834Glu
ENST00000541774.5:c.3283C>G	ENSP00000446466.1:p.Gln1095Glu
ENST00000578373.5:c.*3118C>G	ENSP00000463427.1:n.*3118C>G
ENST00000584450.5:c.3160-226C>G	ENSP00000463714.1:n.3160-226C>G
ENST00000584601.5:c.3238C>G	ENSP00000462438.1:p.Gln1080Glu
NM_001005862.2:c.3238C>G , LRG_724t1:c.3238C>G	NP_001005862.1:p.Gln1080Glu
NM_001289936.1:c.3283C>G , LRG_724t4:c.3283C>G	NP_001276865.1:p.Gln1095Glu
NM_001289937.1:c.3160-226C>G	NP_001276866.1:n.3160-226C>G
NM_004448.3:c.3328C>G , LRG_724t2:c.3328C>G	NP_004439.2:p.Gln1110Glu
NR_110535.1:n.3652C>G
XM_024450641.1:c.3466C>G	XP_024306409.1:p.Gln1156Glu
XM_024450642.1:c.3421C>G	XP_024306410.1:p.Gln1141Glu
XM_024450643.1:c.3376C>G	XP_024306411.1:p.Gln1126Glu
NM_001005862.3:c.3238C>G	NP_001005862.1:p.Gln1080Glu
NM_001289936.2:c.3283C>G	NP_001276865.1:p.Gln1095Glu
NM_001289937.2:c.3160-226C>G	NP_001276866.1:n.3160-226C>G
NM_001382782.1:c.3238C>G	NP_001369711.1:p.Gln1080Glu
NM_001382783.1:c.3238C>G	NP_001369712.1:p.Gln1080Glu
NM_001382784.1:c.3445C>G	NP_001369713.1:p.Gln1149Glu
NM_001382785.1:c.3430C>G	NP_001369714.1:p.Gln1144Glu
NM_001382786.1:c.3409C>G	NP_001369715.1:p.Gln1137Glu
NM_001382787.1:c.3403C>G	NP_001369716.1:p.Gln1135Glu
NM_001382788.1:c.3358C>G	NP_001369717.1:p.Gln1120Glu
NM_001382789.1:c.3349C>G	NP_001369718.1:p.Gln1117Glu
NM_001382790.1:c.3325C>G	NP_001369719.1:p.Gln1109Glu
NM_001382791.1:c.3319C>G	NP_001369720.1:p.Gln1107Glu
NM_001382792.1:c.3292C>G	NP_001369721.1:p.Gln1098Glu
NM_001382793.1:c.3286C>G	NP_001369722.1:p.Gln1096Glu
NM_001382794.1:c.3286C>G	NP_001369723.1:p.Gln1096Glu
NM_001382795.1:c.3280C>G	NP_001369724.1:p.Gln1094Glu
NM_001382796.1:c.3241C>G	NP_001369725.1:p.Gln1081Glu
NM_001382797.1:c.3229C>G	NP_001369726.1:p.Gln1077Glu
NM_001382798.1:c.3172C>G	NP_001369727.1:p.Gln1058Glu
NM_001382799.1:c.3148C>G	NP_001369728.1:p.Gln1050Glu
NM_001382800.1:c.3142C>G	NP_001369729.1:p.Gln1048Glu
NM_001382801.1:c.3124C>G	NP_001369730.1:p.Gln1042Glu
NM_001382802.1:c.3070C>G	NP_001369731.1:p.Gln1024Glu
NM_001382803.1:c.3118-226C>G	NP_001369732.1:n.3118-226C>G
NM_001382804.1:c.2500C>G	NP_001369733.1:p.Gln834Glu
NM_001382805.1:c.2377C>G	NP_001369734.1:p.Gln793Glu
NM_001382806.1:c.2290C>G	NP_001369735.1:p.Gln764Glu
NM_004448.4:c.3328C>G MANE Select	NP_004439.2:p.Gln1110Glu
NR_110535.2:n.3566C>G