Canonical Allele Identifier: CA399313866

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143306375
• MyVariant Identifiers: chr17:g.37884127C>G (hg19) ; chr17:g.39727874C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727874C>G , CM000679.2:g.39727874C>G	GRCh38
NC_000017.10:g.37884127C>G , CM000679.1:g.37884127C>G	GRCh37
NC_000017.9:g.35137653C>G	NCBI36
NG_007503.1:g.44735C>G , LRG_724:g.44735C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3598C>G MANE Select	ENSP00000269571.4:p.Gln1200Glu
ENST00000269571.9:c.3598C>G	ENSP00000269571.4:p.Gln1200Glu
ENST00000406381.6:c.3508C>G	ENSP00000385185.2:p.Gln1170Glu
ENST00000445658.6:c.2770C>G	ENSP00000404047.2:p.Gln924Glu
ENST00000541774.5:c.3553C>G	ENSP00000446466.1:p.Gln1185Glu
ENST00000578373.5:c.*3388C>G	ENSP00000463427.1:n.*3388C>G
ENST00000584450.5:c.*177C>G	ENSP00000463714.1:n.*177C>G
ENST00000584601.5:c.3508C>G	ENSP00000462438.1:p.Gln1170Glu
NM_001005862.2:c.3508C>G , LRG_724t1:c.3508C>G	NP_001005862.1:p.Gln1170Glu
NM_001289936.1:c.3553C>G , LRG_724t4:c.3553C>G	NP_001276865.1:p.Gln1185Glu
NM_001289937.1:c.*177C>G	NP_001276866.1:n.*177C>G
NM_004448.3:c.3598C>G , LRG_724t2:c.3598C>G	NP_004439.2:p.Gln1200Glu
NR_110535.1:n.3922C>G
XM_024450641.1:c.3736C>G	XP_024306409.1:p.Gln1246Glu
XM_024450642.1:c.3691C>G	XP_024306410.1:p.Gln1231Glu
XM_024450643.1:c.3646C>G	XP_024306411.1:p.Gln1216Glu
NM_001005862.3:c.3508C>G	NP_001005862.1:p.Gln1170Glu
NM_001289936.2:c.3553C>G	NP_001276865.1:p.Gln1185Glu
NM_001289937.2:c.*177C>G	NP_001276866.1:n.*177C>G
NM_001382782.1:c.3508C>G	NP_001369711.1:p.Gln1170Glu
NM_001382783.1:c.3508C>G	NP_001369712.1:p.Gln1170Glu
NM_001382784.1:c.3715C>G	NP_001369713.1:p.Gln1239Glu
NM_001382785.1:c.3700C>G	NP_001369714.1:p.Gln1234Glu
NM_001382786.1:c.3679C>G	NP_001369715.1:p.Gln1227Glu
NM_001382787.1:c.3673C>G	NP_001369716.1:p.Gln1225Glu
NM_001382788.1:c.3628C>G	NP_001369717.1:p.Gln1210Glu
NM_001382789.1:c.3619C>G	NP_001369718.1:p.Gln1207Glu
NM_001382790.1:c.3595C>G	NP_001369719.1:p.Gln1199Glu
NM_001382791.1:c.3589C>G	NP_001369720.1:p.Gln1197Glu
NM_001382792.1:c.3562C>G	NP_001369721.1:p.Gln1188Glu
NM_001382793.1:c.3556C>G	NP_001369722.1:p.Gln1186Glu
NM_001382794.1:c.3556C>G	NP_001369723.1:p.Gln1186Glu
NM_001382795.1:c.3550C>G	NP_001369724.1:p.Gln1184Glu
NM_001382796.1:c.3511C>G	NP_001369725.1:p.Gln1171Glu
NM_001382797.1:c.3499C>G	NP_001369726.1:p.Gln1167Glu
NM_001382798.1:c.3442C>G	NP_001369727.1:p.Gln1148Glu
NM_001382799.1:c.3418C>G	NP_001369728.1:p.Gln1140Glu
NM_001382800.1:c.3412C>G	NP_001369729.1:p.Gln1138Glu
NM_001382801.1:c.3394C>G	NP_001369730.1:p.Gln1132Glu
NM_001382802.1:c.3340C>G	NP_001369731.1:p.Gln1114Glu
NM_001382803.1:c.*177C>G	NP_001369732.1:n.*177C>G
NM_001382804.1:c.2770C>G	NP_001369733.1:p.Gln924Glu
NM_001382805.1:c.2647C>G	NP_001369734.1:p.Gln883Glu
NM_001382806.1:c.2560C>G	NP_001369735.1:p.Gln854Glu
NM_004448.4:c.3598C>G MANE Select	NP_004439.2:p.Gln1200Glu
NR_110535.2:n.3836C>G