Canonical Allele Identifier: CA399314195

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37884170G>T (hg19) ; chr17:g.39727917G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727917G>T , CM000679.2:g.39727917G>T	GRCh38
NC_000017.10:g.37884170G>T , CM000679.1:g.37884170G>T	GRCh37
NC_000017.9:g.35137696G>T	NCBI36
NG_007503.1:g.44778G>T , LRG_724:g.44778G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3641G>T MANE Select	ENSP00000269571.4:p.Ser1214Ile
ENST00000269571.9:c.3641G>T	ENSP00000269571.4:p.Ser1214Ile
ENST00000406381.6:c.3551G>T	ENSP00000385185.2:p.Ser1184Ile
ENST00000445658.6:c.2813G>T	ENSP00000404047.2:p.Ser938Ile
ENST00000541774.5:c.3596G>T	ENSP00000446466.1:p.Ser1199Ile
ENST00000578373.5:c.*3431G>T	ENSP00000463427.1:n.*3431G>T
ENST00000584450.5:c.*220G>T	ENSP00000463714.1:n.*220G>T
ENST00000584601.5:c.3551G>T	ENSP00000462438.1:p.Ser1184Ile
NM_001005862.2:c.3551G>T , LRG_724t1:c.3551G>T	NP_001005862.1:p.Ser1184Ile
NM_001289936.1:c.3596G>T , LRG_724t4:c.3596G>T	NP_001276865.1:p.Ser1199Ile
NM_001289937.1:c.*220G>T	NP_001276866.1:n.*220G>T
NM_004448.3:c.3641G>T , LRG_724t2:c.3641G>T	NP_004439.2:p.Ser1214Ile
NR_110535.1:n.3965G>T
XM_024450641.1:c.3779G>T	XP_024306409.1:p.Ser1260Ile
XM_024450642.1:c.3734G>T	XP_024306410.1:p.Ser1245Ile
XM_024450643.1:c.3689G>T	XP_024306411.1:p.Ser1230Ile
NM_001005862.3:c.3551G>T	NP_001005862.1:p.Ser1184Ile
NM_001289936.2:c.3596G>T	NP_001276865.1:p.Ser1199Ile
NM_001289937.2:c.*220G>T	NP_001276866.1:n.*220G>T
NM_001382782.1:c.3551G>T	NP_001369711.1:p.Ser1184Ile
NM_001382783.1:c.3551G>T	NP_001369712.1:p.Ser1184Ile
NM_001382784.1:c.3758G>T	NP_001369713.1:p.Ser1253Ile
NM_001382785.1:c.3743G>T	NP_001369714.1:p.Ser1248Ile
NM_001382786.1:c.3722G>T	NP_001369715.1:p.Ser1241Ile
NM_001382787.1:c.3716G>T	NP_001369716.1:p.Ser1239Ile
NM_001382788.1:c.3671G>T	NP_001369717.1:p.Ser1224Ile
NM_001382789.1:c.3662G>T	NP_001369718.1:p.Ser1221Ile
NM_001382790.1:c.3638G>T	NP_001369719.1:p.Ser1213Ile
NM_001382791.1:c.3632G>T	NP_001369720.1:p.Ser1211Ile
NM_001382792.1:c.3605G>T	NP_001369721.1:p.Ser1202Ile
NM_001382793.1:c.3599G>T	NP_001369722.1:p.Ser1200Ile
NM_001382794.1:c.3599G>T	NP_001369723.1:p.Ser1200Ile
NM_001382795.1:c.3593G>T	NP_001369724.1:p.Ser1198Ile
NM_001382796.1:c.3554G>T	NP_001369725.1:p.Ser1185Ile
NM_001382797.1:c.3542G>T	NP_001369726.1:p.Ser1181Ile
NM_001382798.1:c.3485G>T	NP_001369727.1:p.Ser1162Ile
NM_001382799.1:c.3461G>T	NP_001369728.1:p.Ser1154Ile
NM_001382800.1:c.3455G>T	NP_001369729.1:p.Ser1152Ile
NM_001382801.1:c.3437G>T	NP_001369730.1:p.Ser1146Ile
NM_001382802.1:c.3383G>T	NP_001369731.1:p.Ser1128Ile
NM_001382803.1:c.*220G>T	NP_001369732.1:n.*220G>T
NM_001382804.1:c.2813G>T	NP_001369733.1:p.Ser938Ile
NM_001382805.1:c.2690G>T	NP_001369734.1:p.Ser897Ile
NM_001382806.1:c.2603G>T	NP_001369735.1:p.Ser868Ile
NM_004448.4:c.3641G>T MANE Select	NP_004439.2:p.Ser1214Ile
NR_110535.2:n.3879G>T