Canonical Allele Identifier: CA399313409

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143299612
• MyVariant Identifiers: chr17:g.37884067G>A (hg19) ; chr17:g.39727814G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727814G>A , CM000679.2:g.39727814G>A	GRCh38
NC_000017.10:g.37884067G>A , CM000679.1:g.37884067G>A	GRCh37
NC_000017.9:g.35137593G>A	NCBI36
NG_007503.1:g.44675G>A , LRG_724:g.44675G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3538G>A MANE Select	ENSP00000269571.4:p.Val1180Ile
ENST00000269571.9:c.3538G>A	ENSP00000269571.4:p.Val1180Ile
ENST00000406381.6:c.3448G>A	ENSP00000385185.2:p.Val1150Ile
ENST00000445658.6:c.2710G>A	ENSP00000404047.2:p.Val904Ile
ENST00000541774.5:c.3493G>A	ENSP00000446466.1:p.Val1165Ile
ENST00000578373.5:c.*3328G>A	ENSP00000463427.1:n.*3328G>A
ENST00000584450.5:c.*117G>A	ENSP00000463714.1:n.*117G>A
ENST00000584601.5:c.3448G>A	ENSP00000462438.1:p.Val1150Ile
NM_001005862.2:c.3448G>A , LRG_724t1:c.3448G>A	NP_001005862.1:p.Val1150Ile
NM_001289936.1:c.3493G>A , LRG_724t4:c.3493G>A	NP_001276865.1:p.Val1165Ile
NM_001289937.1:c.*117G>A	NP_001276866.1:n.*117G>A
NM_004448.3:c.3538G>A , LRG_724t2:c.3538G>A	NP_004439.2:p.Val1180Ile
NR_110535.1:n.3862G>A
XM_024450641.1:c.3676G>A	XP_024306409.1:p.Val1226Ile
XM_024450642.1:c.3631G>A	XP_024306410.1:p.Val1211Ile
XM_024450643.1:c.3586G>A	XP_024306411.1:p.Val1196Ile
NM_001005862.3:c.3448G>A	NP_001005862.1:p.Val1150Ile
NM_001289936.2:c.3493G>A	NP_001276865.1:p.Val1165Ile
NM_001289937.2:c.*117G>A	NP_001276866.1:n.*117G>A
NM_001382782.1:c.3448G>A	NP_001369711.1:p.Val1150Ile
NM_001382783.1:c.3448G>A	NP_001369712.1:p.Val1150Ile
NM_001382784.1:c.3655G>A	NP_001369713.1:p.Val1219Ile
NM_001382785.1:c.3640G>A	NP_001369714.1:p.Val1214Ile
NM_001382786.1:c.3619G>A	NP_001369715.1:p.Val1207Ile
NM_001382787.1:c.3613G>A	NP_001369716.1:p.Val1205Ile
NM_001382788.1:c.3568G>A	NP_001369717.1:p.Val1190Ile
NM_001382789.1:c.3559G>A	NP_001369718.1:p.Val1187Ile
NM_001382790.1:c.3535G>A	NP_001369719.1:p.Val1179Ile
NM_001382791.1:c.3529G>A	NP_001369720.1:p.Val1177Ile
NM_001382792.1:c.3502G>A	NP_001369721.1:p.Val1168Ile
NM_001382793.1:c.3496G>A	NP_001369722.1:p.Val1166Ile
NM_001382794.1:c.3496G>A	NP_001369723.1:p.Val1166Ile
NM_001382795.1:c.3490G>A	NP_001369724.1:p.Val1164Ile
NM_001382796.1:c.3451G>A	NP_001369725.1:p.Val1151Ile
NM_001382797.1:c.3439G>A	NP_001369726.1:p.Val1147Ile
NM_001382798.1:c.3382G>A	NP_001369727.1:p.Val1128Ile
NM_001382799.1:c.3358G>A	NP_001369728.1:p.Val1120Ile
NM_001382800.1:c.3352G>A	NP_001369729.1:p.Val1118Ile
NM_001382801.1:c.3334G>A	NP_001369730.1:p.Val1112Ile
NM_001382802.1:c.3280G>A	NP_001369731.1:p.Val1094Ile
NM_001382803.1:c.*117G>A	NP_001369732.1:n.*117G>A
NM_001382804.1:c.2710G>A	NP_001369733.1:p.Val904Ile
NM_001382805.1:c.2587G>A	NP_001369734.1:p.Val863Ile
NM_001382806.1:c.2500G>A	NP_001369735.1:p.Val834Ile
NM_004448.4:c.3538G>A MANE Select	NP_004439.2:p.Val1180Ile
NR_110535.2:n.3776G>A