Canonical Allele Identifier: CA399313724

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143304162
• MyVariant Identifiers: chr17:g.37884107A>G (hg19) ; chr17:g.39727854A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727854A>G , CM000679.2:g.39727854A>G	GRCh38
NC_000017.10:g.37884107A>G , CM000679.1:g.37884107A>G	GRCh37
NC_000017.9:g.35137633A>G	NCBI36
NG_007503.1:g.44715A>G , LRG_724:g.44715A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3578A>G MANE Select	ENSP00000269571.4:p.Asn1193Ser
ENST00000269571.9:c.3578A>G	ENSP00000269571.4:p.Asn1193Ser
ENST00000406381.6:c.3488A>G	ENSP00000385185.2:p.Asn1163Ser
ENST00000445658.6:c.2750A>G	ENSP00000404047.2:p.Asn917Ser
ENST00000541774.5:c.3533A>G	ENSP00000446466.1:p.Asn1178Ser
ENST00000578373.5:c.*3368A>G	ENSP00000463427.1:n.*3368A>G
ENST00000584450.5:c.*157A>G	ENSP00000463714.1:n.*157A>G
ENST00000584601.5:c.3488A>G	ENSP00000462438.1:p.Asn1163Ser
NM_001005862.2:c.3488A>G , LRG_724t1:c.3488A>G	NP_001005862.1:p.Asn1163Ser
NM_001289936.1:c.3533A>G , LRG_724t4:c.3533A>G	NP_001276865.1:p.Asn1178Ser
NM_001289937.1:c.*157A>G	NP_001276866.1:n.*157A>G
NM_004448.3:c.3578A>G , LRG_724t2:c.3578A>G	NP_004439.2:p.Asn1193Ser
NR_110535.1:n.3902A>G
XM_024450641.1:c.3716A>G	XP_024306409.1:p.Asn1239Ser
XM_024450642.1:c.3671A>G	XP_024306410.1:p.Asn1224Ser
XM_024450643.1:c.3626A>G	XP_024306411.1:p.Asn1209Ser
NM_001005862.3:c.3488A>G	NP_001005862.1:p.Asn1163Ser
NM_001289936.2:c.3533A>G	NP_001276865.1:p.Asn1178Ser
NM_001289937.2:c.*157A>G	NP_001276866.1:n.*157A>G
NM_001382782.1:c.3488A>G	NP_001369711.1:p.Asn1163Ser
NM_001382783.1:c.3488A>G	NP_001369712.1:p.Asn1163Ser
NM_001382784.1:c.3695A>G	NP_001369713.1:p.Asn1232Ser
NM_001382785.1:c.3680A>G	NP_001369714.1:p.Asn1227Ser
NM_001382786.1:c.3659A>G	NP_001369715.1:p.Asn1220Ser
NM_001382787.1:c.3653A>G	NP_001369716.1:p.Asn1218Ser
NM_001382788.1:c.3608A>G	NP_001369717.1:p.Asn1203Ser
NM_001382789.1:c.3599A>G	NP_001369718.1:p.Asn1200Ser
NM_001382790.1:c.3575A>G	NP_001369719.1:p.Asn1192Ser
NM_001382791.1:c.3569A>G	NP_001369720.1:p.Asn1190Ser
NM_001382792.1:c.3542A>G	NP_001369721.1:p.Asn1181Ser
NM_001382793.1:c.3536A>G	NP_001369722.1:p.Asn1179Ser
NM_001382794.1:c.3536A>G	NP_001369723.1:p.Asn1179Ser
NM_001382795.1:c.3530A>G	NP_001369724.1:p.Asn1177Ser
NM_001382796.1:c.3491A>G	NP_001369725.1:p.Asn1164Ser
NM_001382797.1:c.3479A>G	NP_001369726.1:p.Asn1160Ser
NM_001382798.1:c.3422A>G	NP_001369727.1:p.Asn1141Ser
NM_001382799.1:c.3398A>G	NP_001369728.1:p.Asn1133Ser
NM_001382800.1:c.3392A>G	NP_001369729.1:p.Asn1131Ser
NM_001382801.1:c.3374A>G	NP_001369730.1:p.Asn1125Ser
NM_001382802.1:c.3320A>G	NP_001369731.1:p.Asn1107Ser
NM_001382803.1:c.*157A>G	NP_001369732.1:n.*157A>G
NM_001382804.1:c.2750A>G	NP_001369733.1:p.Asn917Ser
NM_001382805.1:c.2627A>G	NP_001369734.1:p.Asn876Ser
NM_001382806.1:c.2540A>G	NP_001369735.1:p.Asn847Ser
NM_004448.4:c.3578A>G MANE Select	NP_004439.2:p.Asn1193Ser
NR_110535.2:n.3816A>G