Canonical Allele Identifier: CA399312791

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883794C>G (hg19) ; chr17:g.39727541C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727541C>G , CM000679.2:g.39727541C>G	GRCh38
NC_000017.10:g.37883794C>G , CM000679.1:g.37883794C>G	GRCh37
NC_000017.9:g.35137320C>G	NCBI36
NG_007503.1:g.44402C>G , LRG_724:g.44402C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3406C>G MANE Select	ENSP00000269571.4:p.Gln1136Glu
ENST00000269571.9:c.3406C>G	ENSP00000269571.4:p.Gln1136Glu
ENST00000406381.6:c.3316C>G	ENSP00000385185.2:p.Gln1106Glu
ENST00000445658.6:c.2578C>G	ENSP00000404047.2:p.Gln860Glu
ENST00000541774.5:c.3361C>G	ENSP00000446466.1:p.Gln1121Glu
ENST00000578373.5:c.*3196C>G	ENSP00000463427.1:n.*3196C>G
ENST00000584450.5:c.3160-148C>G	ENSP00000463714.1:n.3160-148C>G
ENST00000584601.5:c.3316C>G	ENSP00000462438.1:p.Gln1106Glu
NM_001005862.2:c.3316C>G , LRG_724t1:c.3316C>G	NP_001005862.1:p.Gln1106Glu
NM_001289936.1:c.3361C>G , LRG_724t4:c.3361C>G	NP_001276865.1:p.Gln1121Glu
NM_001289937.1:c.3160-148C>G	NP_001276866.1:n.3160-148C>G
NM_004448.3:c.3406C>G , LRG_724t2:c.3406C>G	NP_004439.2:p.Gln1136Glu
NR_110535.1:n.3730C>G
XM_024450641.1:c.3544C>G	XP_024306409.1:p.Gln1182Glu
XM_024450642.1:c.3499C>G	XP_024306410.1:p.Gln1167Glu
XM_024450643.1:c.3454C>G	XP_024306411.1:p.Gln1152Glu
NM_001005862.3:c.3316C>G	NP_001005862.1:p.Gln1106Glu
NM_001289936.2:c.3361C>G	NP_001276865.1:p.Gln1121Glu
NM_001289937.2:c.3160-148C>G	NP_001276866.1:n.3160-148C>G
NM_001382782.1:c.3316C>G	NP_001369711.1:p.Gln1106Glu
NM_001382783.1:c.3316C>G	NP_001369712.1:p.Gln1106Glu
NM_001382784.1:c.3523C>G	NP_001369713.1:p.Gln1175Glu
NM_001382785.1:c.3508C>G	NP_001369714.1:p.Gln1170Glu
NM_001382786.1:c.3487C>G	NP_001369715.1:p.Gln1163Glu
NM_001382787.1:c.3481C>G	NP_001369716.1:p.Gln1161Glu
NM_001382788.1:c.3436C>G	NP_001369717.1:p.Gln1146Glu
NM_001382789.1:c.3427C>G	NP_001369718.1:p.Gln1143Glu
NM_001382790.1:c.3403C>G	NP_001369719.1:p.Gln1135Glu
NM_001382791.1:c.3397C>G	NP_001369720.1:p.Gln1133Glu
NM_001382792.1:c.3370C>G	NP_001369721.1:p.Gln1124Glu
NM_001382793.1:c.3364C>G	NP_001369722.1:p.Gln1122Glu
NM_001382794.1:c.3364C>G	NP_001369723.1:p.Gln1122Glu
NM_001382795.1:c.3358C>G	NP_001369724.1:p.Gln1120Glu
NM_001382796.1:c.3319C>G	NP_001369725.1:p.Gln1107Glu
NM_001382797.1:c.3307C>G	NP_001369726.1:p.Gln1103Glu
NM_001382798.1:c.3250C>G	NP_001369727.1:p.Gln1084Glu
NM_001382799.1:c.3226C>G	NP_001369728.1:p.Gln1076Glu
NM_001382800.1:c.3220C>G	NP_001369729.1:p.Gln1074Glu
NM_001382801.1:c.3202C>G	NP_001369730.1:p.Gln1068Glu
NM_001382802.1:c.3148C>G	NP_001369731.1:p.Gln1050Glu
NM_001382803.1:c.3118-148C>G	NP_001369732.1:n.3118-148C>G
NM_001382804.1:c.2578C>G	NP_001369733.1:p.Gln860Glu
NM_001382805.1:c.2455C>G	NP_001369734.1:p.Gln819Glu
NM_001382806.1:c.2368C>G	NP_001369735.1:p.Gln790Glu
NM_004448.4:c.3406C>G MANE Select	NP_004439.2:p.Gln1136Glu
NR_110535.2:n.3644C>G