Canonical Allele Identifier: CA399313727

Gene: ERBB2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3578A>T MANE Select	ENSP00000269571.4:p.Asn1193Ile
ENST00000269571.9:c.3578A>T	ENSP00000269571.4:p.Asn1193Ile
ENST00000406381.6:c.3488A>T	ENSP00000385185.2:p.Asn1163Ile
ENST00000445658.6:c.2750A>T	ENSP00000404047.2:p.Asn917Ile
ENST00000541774.5:c.3533A>T	ENSP00000446466.1:p.Asn1178Ile
ENST00000578373.5:c.*3368A>T	ENSP00000463427.1:n.*3368A>T
ENST00000584450.5:c.*157A>T	ENSP00000463714.1:n.*157A>T
ENST00000584601.5:c.3488A>T	ENSP00000462438.1:p.Asn1163Ile
NM_001005862.2:c.3488A>T , LRG_724t1:c.3488A>T	NP_001005862.1:p.Asn1163Ile
NM_001289936.1:c.3533A>T , LRG_724t4:c.3533A>T	NP_001276865.1:p.Asn1178Ile
NM_001289937.1:c.*157A>T	NP_001276866.1:n.*157A>T
NM_004448.3:c.3578A>T , LRG_724t2:c.3578A>T	NP_004439.2:p.Asn1193Ile
NR_110535.1:n.3902A>T
XM_024450641.1:c.3716A>T	XP_024306409.1:p.Asn1239Ile
XM_024450642.1:c.3671A>T	XP_024306410.1:p.Asn1224Ile
XM_024450643.1:c.3626A>T	XP_024306411.1:p.Asn1209Ile
NM_001005862.3:c.3488A>T	NP_001005862.1:p.Asn1163Ile
NM_001289936.2:c.3533A>T	NP_001276865.1:p.Asn1178Ile
NM_001289937.2:c.*157A>T	NP_001276866.1:n.*157A>T
NM_001382782.1:c.3488A>T	NP_001369711.1:p.Asn1163Ile
NM_001382783.1:c.3488A>T	NP_001369712.1:p.Asn1163Ile
NM_001382784.1:c.3695A>T	NP_001369713.1:p.Asn1232Ile
NM_001382785.1:c.3680A>T	NP_001369714.1:p.Asn1227Ile
NM_001382786.1:c.3659A>T	NP_001369715.1:p.Asn1220Ile
NM_001382787.1:c.3653A>T	NP_001369716.1:p.Asn1218Ile
NM_001382788.1:c.3608A>T	NP_001369717.1:p.Asn1203Ile
NM_001382789.1:c.3599A>T	NP_001369718.1:p.Asn1200Ile
NM_001382790.1:c.3575A>T	NP_001369719.1:p.Asn1192Ile
NM_001382791.1:c.3569A>T	NP_001369720.1:p.Asn1190Ile
NM_001382792.1:c.3542A>T	NP_001369721.1:p.Asn1181Ile
NM_001382793.1:c.3536A>T	NP_001369722.1:p.Asn1179Ile
NM_001382794.1:c.3536A>T	NP_001369723.1:p.Asn1179Ile
NM_001382795.1:c.3530A>T	NP_001369724.1:p.Asn1177Ile
NM_001382796.1:c.3491A>T	NP_001369725.1:p.Asn1164Ile
NM_001382797.1:c.3479A>T	NP_001369726.1:p.Asn1160Ile
NM_001382798.1:c.3422A>T	NP_001369727.1:p.Asn1141Ile
NM_001382799.1:c.3398A>T	NP_001369728.1:p.Asn1133Ile
NM_001382800.1:c.3392A>T	NP_001369729.1:p.Asn1131Ile
NM_001382801.1:c.3374A>T	NP_001369730.1:p.Asn1125Ile
NM_001382802.1:c.3320A>T	NP_001369731.1:p.Asn1107Ile
NM_001382803.1:c.*157A>T	NP_001369732.1:n.*157A>T
NM_001382804.1:c.2750A>T	NP_001369733.1:p.Asn917Ile
NM_001382805.1:c.2627A>T	NP_001369734.1:p.Asn876Ile
NM_001382806.1:c.2540A>T	NP_001369735.1:p.Asn847Ile
NM_004448.4:c.3578A>T MANE Select	NP_004439.2:p.Asn1193Ile
NR_110535.2:n.3816A>T