Canonical Allele Identifier: CA399310700

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143246377
• MyVariant Identifiers: chr17:g.37883672C>G (hg19) ; chr17:g.39727419C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727419C>G , CM000679.2:g.39727419C>G	GRCh38
NC_000017.10:g.37883672C>G , CM000679.1:g.37883672C>G	GRCh37
NC_000017.9:g.35137198C>G	NCBI36
NG_007503.1:g.44280C>G , LRG_724:g.44280C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3284C>G MANE Select	ENSP00000269571.4:p.Ala1095Gly
ENST00000269571.9:c.3284C>G	ENSP00000269571.4:p.Ala1095Gly
ENST00000406381.6:c.3194C>G	ENSP00000385185.2:p.Ala1065Gly
ENST00000445658.6:c.2456C>G	ENSP00000404047.2:p.Ala819Gly
ENST00000541774.5:c.3239C>G	ENSP00000446466.1:p.Ala1080Gly
ENST00000578373.5:c.*3074C>G	ENSP00000463427.1:n.*3074C>G
ENST00000584450.5:c.3160-270C>G	ENSP00000463714.1:n.3160-270C>G
ENST00000584601.5:c.3194C>G	ENSP00000462438.1:p.Ala1065Gly
NM_001005862.2:c.3194C>G , LRG_724t1:c.3194C>G	NP_001005862.1:p.Ala1065Gly
NM_001289936.1:c.3239C>G , LRG_724t4:c.3239C>G	NP_001276865.1:p.Ala1080Gly
NM_001289937.1:c.3160-270C>G	NP_001276866.1:n.3160-270C>G
NM_004448.3:c.3284C>G , LRG_724t2:c.3284C>G	NP_004439.2:p.Ala1095Gly
NR_110535.1:n.3608C>G
XM_024450641.1:c.3422C>G	XP_024306409.1:p.Ala1141Gly
XM_024450642.1:c.3377C>G	XP_024306410.1:p.Ala1126Gly
XM_024450643.1:c.3332C>G	XP_024306411.1:p.Ala1111Gly
NM_001005862.3:c.3194C>G	NP_001005862.1:p.Ala1065Gly
NM_001289936.2:c.3239C>G	NP_001276865.1:p.Ala1080Gly
NM_001289937.2:c.3160-270C>G	NP_001276866.1:n.3160-270C>G
NM_001382782.1:c.3194C>G	NP_001369711.1:p.Ala1065Gly
NM_001382783.1:c.3194C>G	NP_001369712.1:p.Ala1065Gly
NM_001382784.1:c.3401C>G	NP_001369713.1:p.Ala1134Gly
NM_001382785.1:c.3386C>G	NP_001369714.1:p.Ala1129Gly
NM_001382786.1:c.3365C>G	NP_001369715.1:p.Ala1122Gly
NM_001382787.1:c.3359C>G	NP_001369716.1:p.Ala1120Gly
NM_001382788.1:c.3314C>G	NP_001369717.1:p.Ala1105Gly
NM_001382789.1:c.3305C>G	NP_001369718.1:p.Ala1102Gly
NM_001382790.1:c.3281C>G	NP_001369719.1:p.Ala1094Gly
NM_001382791.1:c.3275C>G	NP_001369720.1:p.Ala1092Gly
NM_001382792.1:c.3248C>G	NP_001369721.1:p.Ala1083Gly
NM_001382793.1:c.3242C>G	NP_001369722.1:p.Ala1081Gly
NM_001382794.1:c.3242C>G	NP_001369723.1:p.Ala1081Gly
NM_001382795.1:c.3236C>G	NP_001369724.1:p.Ala1079Gly
NM_001382796.1:c.3197C>G	NP_001369725.1:p.Ala1066Gly
NM_001382797.1:c.3185C>G	NP_001369726.1:p.Ala1062Gly
NM_001382798.1:c.3128C>G	NP_001369727.1:p.Ala1043Gly
NM_001382799.1:c.3104C>G	NP_001369728.1:p.Ala1035Gly
NM_001382800.1:c.3098C>G	NP_001369729.1:p.Ala1033Gly
NM_001382801.1:c.3080C>G	NP_001369730.1:p.Ala1027Gly
NM_001382802.1:c.3026C>G	NP_001369731.1:p.Ala1009Gly
NM_001382803.1:c.3118-270C>G	NP_001369732.1:n.3118-270C>G
NM_001382804.1:c.2456C>G	NP_001369733.1:p.Ala819Gly
NM_001382805.1:c.2333C>G	NP_001369734.1:p.Ala778Gly
NM_001382806.1:c.2246C>G	NP_001369735.1:p.Ala749Gly
NM_004448.4:c.3284C>G MANE Select	NP_004439.2:p.Ala1095Gly
NR_110535.2:n.3522C>G