Canonical Allele Identifier: CA399312844

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883953C>G (hg19) ; chr17:g.39727700C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727700C>G , CM000679.2:g.39727700C>G	GRCh38
NC_000017.10:g.37883953C>G , CM000679.1:g.37883953C>G	GRCh37
NC_000017.9:g.35137479C>G	NCBI36
NG_007503.1:g.44561C>G , LRG_724:g.44561C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3424C>G MANE Select	ENSP00000269571.4:p.Gln1142Glu
ENST00000269571.9:c.3424C>G	ENSP00000269571.4:p.Gln1142Glu
ENST00000406381.6:c.3334C>G	ENSP00000385185.2:p.Gln1112Glu
ENST00000445658.6:c.2596C>G	ENSP00000404047.2:p.Gln866Glu
ENST00000541774.5:c.3379C>G	ENSP00000446466.1:p.Gln1127Glu
ENST00000578373.5:c.*3214C>G	ENSP00000463427.1:n.*3214C>G
ENST00000584450.5:c.*3C>G	ENSP00000463714.1:n.*3C>G
ENST00000584601.5:c.3334C>G	ENSP00000462438.1:p.Gln1112Glu
NM_001005862.2:c.3334C>G , LRG_724t1:c.3334C>G	NP_001005862.1:p.Gln1112Glu
NM_001289936.1:c.3379C>G , LRG_724t4:c.3379C>G	NP_001276865.1:p.Gln1127Glu
NM_001289937.1:c.*3C>G	NP_001276866.1:n.*3C>G
NM_004448.3:c.3424C>G , LRG_724t2:c.3424C>G	NP_004439.2:p.Gln1142Glu
NR_110535.1:n.3748C>G
XM_024450641.1:c.3562C>G	XP_024306409.1:p.Gln1188Glu
XM_024450642.1:c.3517C>G	XP_024306410.1:p.Gln1173Glu
XM_024450643.1:c.3472C>G	XP_024306411.1:p.Gln1158Glu
NM_001005862.3:c.3334C>G	NP_001005862.1:p.Gln1112Glu
NM_001289936.2:c.3379C>G	NP_001276865.1:p.Gln1127Glu
NM_001289937.2:c.*3C>G	NP_001276866.1:n.*3C>G
NM_001382782.1:c.3334C>G	NP_001369711.1:p.Gln1112Glu
NM_001382783.1:c.3334C>G	NP_001369712.1:p.Gln1112Glu
NM_001382784.1:c.3541C>G	NP_001369713.1:p.Gln1181Glu
NM_001382785.1:c.3526C>G	NP_001369714.1:p.Gln1176Glu
NM_001382786.1:c.3505C>G	NP_001369715.1:p.Gln1169Glu
NM_001382787.1:c.3499C>G	NP_001369716.1:p.Gln1167Glu
NM_001382788.1:c.3454C>G	NP_001369717.1:p.Gln1152Glu
NM_001382789.1:c.3445C>G	NP_001369718.1:p.Gln1149Glu
NM_001382790.1:c.3421C>G	NP_001369719.1:p.Gln1141Glu
NM_001382791.1:c.3415C>G	NP_001369720.1:p.Gln1139Glu
NM_001382792.1:c.3388C>G	NP_001369721.1:p.Gln1130Glu
NM_001382793.1:c.3382C>G	NP_001369722.1:p.Gln1128Glu
NM_001382794.1:c.3382C>G	NP_001369723.1:p.Gln1128Glu
NM_001382795.1:c.3376C>G	NP_001369724.1:p.Gln1126Glu
NM_001382796.1:c.3337C>G	NP_001369725.1:p.Gln1113Glu
NM_001382797.1:c.3325C>G	NP_001369726.1:p.Gln1109Glu
NM_001382798.1:c.3268C>G	NP_001369727.1:p.Gln1090Glu
NM_001382799.1:c.3244C>G	NP_001369728.1:p.Gln1082Glu
NM_001382800.1:c.3238C>G	NP_001369729.1:p.Gln1080Glu
NM_001382801.1:c.3220C>G	NP_001369730.1:p.Gln1074Glu
NM_001382802.1:c.3166C>G	NP_001369731.1:p.Gln1056Glu
NM_001382803.1:c.*3C>G	NP_001369732.1:n.*3C>G
NM_001382804.1:c.2596C>G	NP_001369733.1:p.Gln866Glu
NM_001382805.1:c.2473C>G	NP_001369734.1:p.Gln825Glu
NM_001382806.1:c.2386C>G	NP_001369735.1:p.Gln796Glu
NM_004448.4:c.3424C>G MANE Select	NP_004439.2:p.Gln1142Glu
NR_110535.2:n.3662C>G