Canonical Allele Identifier: CA399314369

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143313162
• MyVariant Identifiers: chr17:g.37884193T>A (hg19) ; chr17:g.39727940T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727940T>A , CM000679.2:g.39727940T>A	GRCh38
NC_000017.10:g.37884193T>A , CM000679.1:g.37884193T>A	GRCh37
NC_000017.9:g.35137719T>A	NCBI36
NG_007503.1:g.44801T>A , LRG_724:g.44801T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3664T>A MANE Select	ENSP00000269571.4:p.Tyr1222Asn
ENST00000269571.9:c.3664T>A	ENSP00000269571.4:p.Tyr1222Asn
ENST00000406381.6:c.3574T>A	ENSP00000385185.2:p.Tyr1192Asn
ENST00000445658.6:c.2836T>A	ENSP00000404047.2:p.Tyr946Asn
ENST00000541774.5:c.3619T>A	ENSP00000446466.1:p.Tyr1207Asn
ENST00000578373.5:c.*3454T>A	ENSP00000463427.1:n.*3454T>A
ENST00000584450.5:c.*243T>A	ENSP00000463714.1:n.*243T>A
ENST00000584601.5:c.3574T>A	ENSP00000462438.1:p.Tyr1192Asn
NM_001005862.2:c.3574T>A , LRG_724t1:c.3574T>A	NP_001005862.1:p.Tyr1192Asn
NM_001289936.1:c.3619T>A , LRG_724t4:c.3619T>A	NP_001276865.1:p.Tyr1207Asn
NM_001289937.1:c.*243T>A	NP_001276866.1:n.*243T>A
NM_004448.3:c.3664T>A , LRG_724t2:c.3664T>A	NP_004439.2:p.Tyr1222Asn
NR_110535.1:n.3988T>A
XM_024450641.1:c.3802T>A	XP_024306409.1:p.Tyr1268Asn
XM_024450642.1:c.3757T>A	XP_024306410.1:p.Tyr1253Asn
XM_024450643.1:c.3712T>A	XP_024306411.1:p.Tyr1238Asn
NM_001005862.3:c.3574T>A	NP_001005862.1:p.Tyr1192Asn
NM_001289936.2:c.3619T>A	NP_001276865.1:p.Tyr1207Asn
NM_001289937.2:c.*243T>A	NP_001276866.1:n.*243T>A
NM_001382782.1:c.3574T>A	NP_001369711.1:p.Tyr1192Asn
NM_001382783.1:c.3574T>A	NP_001369712.1:p.Tyr1192Asn
NM_001382784.1:c.3781T>A	NP_001369713.1:p.Tyr1261Asn
NM_001382785.1:c.3766T>A	NP_001369714.1:p.Tyr1256Asn
NM_001382786.1:c.3745T>A	NP_001369715.1:p.Tyr1249Asn
NM_001382787.1:c.3739T>A	NP_001369716.1:p.Tyr1247Asn
NM_001382788.1:c.3694T>A	NP_001369717.1:p.Tyr1232Asn
NM_001382789.1:c.3685T>A	NP_001369718.1:p.Tyr1229Asn
NM_001382790.1:c.3661T>A	NP_001369719.1:p.Tyr1221Asn
NM_001382791.1:c.3655T>A	NP_001369720.1:p.Tyr1219Asn
NM_001382792.1:c.3628T>A	NP_001369721.1:p.Tyr1210Asn
NM_001382793.1:c.3622T>A	NP_001369722.1:p.Tyr1208Asn
NM_001382794.1:c.3622T>A	NP_001369723.1:p.Tyr1208Asn
NM_001382795.1:c.3616T>A	NP_001369724.1:p.Tyr1206Asn
NM_001382796.1:c.3577T>A	NP_001369725.1:p.Tyr1193Asn
NM_001382797.1:c.3565T>A	NP_001369726.1:p.Tyr1189Asn
NM_001382798.1:c.3508T>A	NP_001369727.1:p.Tyr1170Asn
NM_001382799.1:c.3484T>A	NP_001369728.1:p.Tyr1162Asn
NM_001382800.1:c.3478T>A	NP_001369729.1:p.Tyr1160Asn
NM_001382801.1:c.3460T>A	NP_001369730.1:p.Tyr1154Asn
NM_001382802.1:c.3406T>A	NP_001369731.1:p.Tyr1136Asn
NM_001382803.1:c.*243T>A	NP_001369732.1:n.*243T>A
NM_001382804.1:c.2836T>A	NP_001369733.1:p.Tyr946Asn
NM_001382805.1:c.2713T>A	NP_001369734.1:p.Tyr905Asn
NM_001382806.1:c.2626T>A	NP_001369735.1:p.Tyr876Asn
NM_004448.4:c.3664T>A MANE Select	NP_004439.2:p.Tyr1222Asn
NR_110535.2:n.3902T>A