Canonical Allele Identifier: CA399313413

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884067G>T (hg19) ; chr17:g.39727814G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3538G>T MANE Select	ENSP00000269571.4:p.Val1180Phe
ENST00000269571.9:c.3538G>T	ENSP00000269571.4:p.Val1180Phe
ENST00000406381.6:c.3448G>T	ENSP00000385185.2:p.Val1150Phe
ENST00000445658.6:c.2710G>T	ENSP00000404047.2:p.Val904Phe
ENST00000541774.5:c.3493G>T	ENSP00000446466.1:p.Val1165Phe
ENST00000578373.5:c.*3328G>T	ENSP00000463427.1:n.*3328G>T
ENST00000584450.5:c.*117G>T	ENSP00000463714.1:n.*117G>T
ENST00000584601.5:c.3448G>T	ENSP00000462438.1:p.Val1150Phe
NM_001005862.2:c.3448G>T , LRG_724t1:c.3448G>T	NP_001005862.1:p.Val1150Phe
NM_001289936.1:c.3493G>T , LRG_724t4:c.3493G>T	NP_001276865.1:p.Val1165Phe
NM_001289937.1:c.*117G>T	NP_001276866.1:n.*117G>T
NM_004448.3:c.3538G>T , LRG_724t2:c.3538G>T	NP_004439.2:p.Val1180Phe
NR_110535.1:n.3862G>T
XM_024450641.1:c.3676G>T	XP_024306409.1:p.Val1226Phe
XM_024450642.1:c.3631G>T	XP_024306410.1:p.Val1211Phe
XM_024450643.1:c.3586G>T	XP_024306411.1:p.Val1196Phe
NM_001005862.3:c.3448G>T	NP_001005862.1:p.Val1150Phe
NM_001289936.2:c.3493G>T	NP_001276865.1:p.Val1165Phe
NM_001289937.2:c.*117G>T	NP_001276866.1:n.*117G>T
NM_001382782.1:c.3448G>T	NP_001369711.1:p.Val1150Phe
NM_001382783.1:c.3448G>T	NP_001369712.1:p.Val1150Phe
NM_001382784.1:c.3655G>T	NP_001369713.1:p.Val1219Phe
NM_001382785.1:c.3640G>T	NP_001369714.1:p.Val1214Phe
NM_001382786.1:c.3619G>T	NP_001369715.1:p.Val1207Phe
NM_001382787.1:c.3613G>T	NP_001369716.1:p.Val1205Phe
NM_001382788.1:c.3568G>T	NP_001369717.1:p.Val1190Phe
NM_001382789.1:c.3559G>T	NP_001369718.1:p.Val1187Phe
NM_001382790.1:c.3535G>T	NP_001369719.1:p.Val1179Phe
NM_001382791.1:c.3529G>T	NP_001369720.1:p.Val1177Phe
NM_001382792.1:c.3502G>T	NP_001369721.1:p.Val1168Phe
NM_001382793.1:c.3496G>T	NP_001369722.1:p.Val1166Phe
NM_001382794.1:c.3496G>T	NP_001369723.1:p.Val1166Phe
NM_001382795.1:c.3490G>T	NP_001369724.1:p.Val1164Phe
NM_001382796.1:c.3451G>T	NP_001369725.1:p.Val1151Phe
NM_001382797.1:c.3439G>T	NP_001369726.1:p.Val1147Phe
NM_001382798.1:c.3382G>T	NP_001369727.1:p.Val1128Phe
NM_001382799.1:c.3358G>T	NP_001369728.1:p.Val1120Phe
NM_001382800.1:c.3352G>T	NP_001369729.1:p.Val1118Phe
NM_001382801.1:c.3334G>T	NP_001369730.1:p.Val1112Phe
NM_001382802.1:c.3280G>T	NP_001369731.1:p.Val1094Phe
NM_001382803.1:c.*117G>T	NP_001369732.1:n.*117G>T
NM_001382804.1:c.2710G>T	NP_001369733.1:p.Val904Phe
NM_001382805.1:c.2587G>T	NP_001369734.1:p.Val863Phe
NM_001382806.1:c.2500G>T	NP_001369735.1:p.Val834Phe
NM_004448.4:c.3538G>T MANE Select	NP_004439.2:p.Val1180Phe
NR_110535.2:n.3776G>T