Canonical Allele Identifier: CA499890295

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143259972
• MyVariant Identifiers: chr17:g.37883784C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727531C>A , CM000679.2:g.39727531C>A	GRCh38
NC_000017.10:g.37883784C>A , CM000679.1:g.37883784C>A	GRCh37
NC_000017.9:g.35137310C>A	NCBI36
NG_007503.1:g.44392C>A , LRG_724:g.44392C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3396C>A MANE Select	ENSP00000269571.4:p.Thr1132=
ENST00000269571.9:c.3396C>A	ENSP00000269571.4:p.Thr1132=
ENST00000406381.6:c.3306C>A	ENSP00000385185.2:p.Thr1102=
ENST00000445658.6:c.2568C>A	ENSP00000404047.2:p.Thr856=
ENST00000541774.5:c.3351C>A	ENSP00000446466.1:p.Thr1117=
ENST00000578373.5:c.*3186C>A	ENSP00000463427.1:n.*3186C>A
ENST00000584450.5:c.3160-158C>A	ENSP00000463714.1:n.3160-158C>A
ENST00000584601.5:c.3306C>A	ENSP00000462438.1:p.Thr1102=
NM_001005862.2:c.3306C>A , LRG_724t1:c.3306C>A	NP_001005862.1:p.Thr1102=
NM_001289936.1:c.3351C>A , LRG_724t4:c.3351C>A	NP_001276865.1:p.Thr1117=
NM_001289937.1:c.3160-158C>A	NP_001276866.1:n.3160-158C>A
NM_004448.3:c.3396C>A , LRG_724t2:c.3396C>A	NP_004439.2:p.Thr1132=
NR_110535.1:n.3720C>A
XM_024450641.1:c.3534C>A	XP_024306409.1:p.Thr1178=
XM_024450642.1:c.3489C>A	XP_024306410.1:p.Thr1163=
XM_024450643.1:c.3444C>A	XP_024306411.1:p.Thr1148=
NM_001005862.3:c.3306C>A	NP_001005862.1:p.Thr1102=
NM_001289936.2:c.3351C>A	NP_001276865.1:p.Thr1117=
NM_001289937.2:c.3160-158C>A	NP_001276866.1:n.3160-158C>A
NM_001382782.1:c.3306C>A	NP_001369711.1:p.Thr1102=
NM_001382783.1:c.3306C>A	NP_001369712.1:p.Thr1102=
NM_001382784.1:c.3513C>A	NP_001369713.1:p.Thr1171=
NM_001382785.1:c.3498C>A	NP_001369714.1:p.Thr1166=
NM_001382786.1:c.3477C>A	NP_001369715.1:p.Thr1159=
NM_001382787.1:c.3471C>A	NP_001369716.1:p.Thr1157=
NM_001382788.1:c.3426C>A	NP_001369717.1:p.Thr1142=
NM_001382789.1:c.3417C>A	NP_001369718.1:p.Thr1139=
NM_001382790.1:c.3393C>A	NP_001369719.1:p.Thr1131=
NM_001382791.1:c.3387C>A	NP_001369720.1:p.Thr1129=
NM_001382792.1:c.3360C>A	NP_001369721.1:p.Thr1120=
NM_001382793.1:c.3354C>A	NP_001369722.1:p.Thr1118=
NM_001382794.1:c.3354C>A	NP_001369723.1:p.Thr1118=
NM_001382795.1:c.3348C>A	NP_001369724.1:p.Thr1116=
NM_001382796.1:c.3309C>A	NP_001369725.1:p.Thr1103=
NM_001382797.1:c.3297C>A	NP_001369726.1:p.Thr1099=
NM_001382798.1:c.3240C>A	NP_001369727.1:p.Thr1080=
NM_001382799.1:c.3216C>A	NP_001369728.1:p.Thr1072=
NM_001382800.1:c.3210C>A	NP_001369729.1:p.Thr1070=
NM_001382801.1:c.3192C>A	NP_001369730.1:p.Thr1064=
NM_001382802.1:c.3138C>A	NP_001369731.1:p.Thr1046=
NM_001382803.1:c.3118-158C>A	NP_001369732.1:n.3118-158C>A
NM_001382804.1:c.2568C>A	NP_001369733.1:p.Thr856=
NM_001382805.1:c.2445C>A	NP_001369734.1:p.Thr815=
NM_001382806.1:c.2358C>A	NP_001369735.1:p.Thr786=
NM_004448.4:c.3396C>A MANE Select	NP_004439.2:p.Thr1132=
NR_110535.2:n.3634C>A