Canonical Allele Identifier: CA399314241

Gene: ERBB2

Linked Data

• dbSNP Id: rs55943169
• MyVariant Identifiers: chr17:g.37884176C>G (hg19) ; chr17:g.39727923C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727923C>G , CM000679.2:g.39727923C>G	GRCh38
NC_000017.10:g.37884176C>G , CM000679.1:g.37884176C>G	GRCh37
NC_000017.9:g.35137702C>G	NCBI36
NG_007503.1:g.44784C>G , LRG_724:g.44784C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3647C>G MANE Select	ENSP00000269571.4:p.Ala1216Gly
ENST00000269571.9:c.3647C>G	ENSP00000269571.4:p.Ala1216Gly
ENST00000406381.6:c.3557C>G	ENSP00000385185.2:p.Ala1186Gly
ENST00000445658.6:c.2819C>G	ENSP00000404047.2:p.Ala940Gly
ENST00000541774.5:c.3602C>G	ENSP00000446466.1:p.Ala1201Gly
ENST00000578373.5:c.*3437C>G	ENSP00000463427.1:n.*3437C>G
ENST00000584450.5:c.*226C>G	ENSP00000463714.1:n.*226C>G
ENST00000584601.5:c.3557C>G	ENSP00000462438.1:p.Ala1186Gly
NM_001005862.2:c.3557C>G , LRG_724t1:c.3557C>G	NP_001005862.1:p.Ala1186Gly
NM_001289936.1:c.3602C>G , LRG_724t4:c.3602C>G	NP_001276865.1:p.Ala1201Gly
NM_001289937.1:c.*226C>G	NP_001276866.1:n.*226C>G
NM_004448.3:c.3647C>G , LRG_724t2:c.3647C>G	NP_004439.2:p.Ala1216Gly
NR_110535.1:n.3971C>G
XM_024450641.1:c.3785C>G	XP_024306409.1:p.Ala1262Gly
XM_024450642.1:c.3740C>G	XP_024306410.1:p.Ala1247Gly
XM_024450643.1:c.3695C>G	XP_024306411.1:p.Ala1232Gly
NM_001005862.3:c.3557C>G	NP_001005862.1:p.Ala1186Gly
NM_001289936.2:c.3602C>G	NP_001276865.1:p.Ala1201Gly
NM_001289937.2:c.*226C>G	NP_001276866.1:n.*226C>G
NM_001382782.1:c.3557C>G	NP_001369711.1:p.Ala1186Gly
NM_001382783.1:c.3557C>G	NP_001369712.1:p.Ala1186Gly
NM_001382784.1:c.3764C>G	NP_001369713.1:p.Ala1255Gly
NM_001382785.1:c.3749C>G	NP_001369714.1:p.Ala1250Gly
NM_001382786.1:c.3728C>G	NP_001369715.1:p.Ala1243Gly
NM_001382787.1:c.3722C>G	NP_001369716.1:p.Ala1241Gly
NM_001382788.1:c.3677C>G	NP_001369717.1:p.Ala1226Gly
NM_001382789.1:c.3668C>G	NP_001369718.1:p.Ala1223Gly
NM_001382790.1:c.3644C>G	NP_001369719.1:p.Ala1215Gly
NM_001382791.1:c.3638C>G	NP_001369720.1:p.Ala1213Gly
NM_001382792.1:c.3611C>G	NP_001369721.1:p.Ala1204Gly
NM_001382793.1:c.3605C>G	NP_001369722.1:p.Ala1202Gly
NM_001382794.1:c.3605C>G	NP_001369723.1:p.Ala1202Gly
NM_001382795.1:c.3599C>G	NP_001369724.1:p.Ala1200Gly
NM_001382796.1:c.3560C>G	NP_001369725.1:p.Ala1187Gly
NM_001382797.1:c.3548C>G	NP_001369726.1:p.Ala1183Gly
NM_001382798.1:c.3491C>G	NP_001369727.1:p.Ala1164Gly
NM_001382799.1:c.3467C>G	NP_001369728.1:p.Ala1156Gly
NM_001382800.1:c.3461C>G	NP_001369729.1:p.Ala1154Gly
NM_001382801.1:c.3443C>G	NP_001369730.1:p.Ala1148Gly
NM_001382802.1:c.3389C>G	NP_001369731.1:p.Ala1130Gly
NM_001382803.1:c.*226C>G	NP_001369732.1:n.*226C>G
NM_001382804.1:c.2819C>G	NP_001369733.1:p.Ala940Gly
NM_001382805.1:c.2696C>G	NP_001369734.1:p.Ala899Gly
NM_001382806.1:c.2609C>G	NP_001369735.1:p.Ala870Gly
NM_004448.4:c.3647C>G MANE Select	NP_004439.2:p.Ala1216Gly
NR_110535.2:n.3885C>G