Canonical Allele Identifier: CA399314367

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884193T>G (hg19) ; chr17:g.39727940T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3664T>G MANE Select	ENSP00000269571.4:p.Tyr1222Asp
ENST00000269571.9:c.3664T>G	ENSP00000269571.4:p.Tyr1222Asp
ENST00000406381.6:c.3574T>G	ENSP00000385185.2:p.Tyr1192Asp
ENST00000445658.6:c.2836T>G	ENSP00000404047.2:p.Tyr946Asp
ENST00000541774.5:c.3619T>G	ENSP00000446466.1:p.Tyr1207Asp
ENST00000578373.5:c.*3454T>G	ENSP00000463427.1:n.*3454T>G
ENST00000584450.5:c.*243T>G	ENSP00000463714.1:n.*243T>G
ENST00000584601.5:c.3574T>G	ENSP00000462438.1:p.Tyr1192Asp
NM_001005862.2:c.3574T>G , LRG_724t1:c.3574T>G	NP_001005862.1:p.Tyr1192Asp
NM_001289936.1:c.3619T>G , LRG_724t4:c.3619T>G	NP_001276865.1:p.Tyr1207Asp
NM_001289937.1:c.*243T>G	NP_001276866.1:n.*243T>G
NM_004448.3:c.3664T>G , LRG_724t2:c.3664T>G	NP_004439.2:p.Tyr1222Asp
NR_110535.1:n.3988T>G
XM_024450641.1:c.3802T>G	XP_024306409.1:p.Tyr1268Asp
XM_024450642.1:c.3757T>G	XP_024306410.1:p.Tyr1253Asp
XM_024450643.1:c.3712T>G	XP_024306411.1:p.Tyr1238Asp
NM_001005862.3:c.3574T>G	NP_001005862.1:p.Tyr1192Asp
NM_001289936.2:c.3619T>G	NP_001276865.1:p.Tyr1207Asp
NM_001289937.2:c.*243T>G	NP_001276866.1:n.*243T>G
NM_001382782.1:c.3574T>G	NP_001369711.1:p.Tyr1192Asp
NM_001382783.1:c.3574T>G	NP_001369712.1:p.Tyr1192Asp
NM_001382784.1:c.3781T>G	NP_001369713.1:p.Tyr1261Asp
NM_001382785.1:c.3766T>G	NP_001369714.1:p.Tyr1256Asp
NM_001382786.1:c.3745T>G	NP_001369715.1:p.Tyr1249Asp
NM_001382787.1:c.3739T>G	NP_001369716.1:p.Tyr1247Asp
NM_001382788.1:c.3694T>G	NP_001369717.1:p.Tyr1232Asp
NM_001382789.1:c.3685T>G	NP_001369718.1:p.Tyr1229Asp
NM_001382790.1:c.3661T>G	NP_001369719.1:p.Tyr1221Asp
NM_001382791.1:c.3655T>G	NP_001369720.1:p.Tyr1219Asp
NM_001382792.1:c.3628T>G	NP_001369721.1:p.Tyr1210Asp
NM_001382793.1:c.3622T>G	NP_001369722.1:p.Tyr1208Asp
NM_001382794.1:c.3622T>G	NP_001369723.1:p.Tyr1208Asp
NM_001382795.1:c.3616T>G	NP_001369724.1:p.Tyr1206Asp
NM_001382796.1:c.3577T>G	NP_001369725.1:p.Tyr1193Asp
NM_001382797.1:c.3565T>G	NP_001369726.1:p.Tyr1189Asp
NM_001382798.1:c.3508T>G	NP_001369727.1:p.Tyr1170Asp
NM_001382799.1:c.3484T>G	NP_001369728.1:p.Tyr1162Asp
NM_001382800.1:c.3478T>G	NP_001369729.1:p.Tyr1160Asp
NM_001382801.1:c.3460T>G	NP_001369730.1:p.Tyr1154Asp
NM_001382802.1:c.3406T>G	NP_001369731.1:p.Tyr1136Asp
NM_001382803.1:c.*243T>G	NP_001369732.1:n.*243T>G
NM_001382804.1:c.2836T>G	NP_001369733.1:p.Tyr946Asp
NM_001382805.1:c.2713T>G	NP_001369734.1:p.Tyr905Asp
NM_001382806.1:c.2626T>G	NP_001369735.1:p.Tyr876Asp
NM_004448.4:c.3664T>G MANE Select	NP_004439.2:p.Tyr1222Asp
NR_110535.2:n.3902T>G