Canonical Allele Identifier: CA399313615

Gene: ERBB2

Linked Data

• dbSNP Id: rs1411396765
• gnomAD v2: 17-37884092-G-T
• MyVariant Identifiers: chr17:g.37884092G>T (hg19) ; chr17:g.39727839G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727839G>T , CM000679.2:g.39727839G>T	GRCh38
NC_000017.10:g.37884092G>T , CM000679.1:g.37884092G>T	GRCh37
NC_000017.9:g.35137618G>T	NCBI36
NG_007503.1:g.44700G>T , LRG_724:g.44700G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3563G>T MANE Select	ENSP00000269571.4:p.Gly1188Val
ENST00000269571.9:c.3563G>T	ENSP00000269571.4:p.Gly1188Val
ENST00000406381.6:c.3473G>T	ENSP00000385185.2:p.Gly1158Val
ENST00000445658.6:c.2735G>T	ENSP00000404047.2:p.Gly912Val
ENST00000541774.5:c.3518G>T	ENSP00000446466.1:p.Gly1173Val
ENST00000578373.5:c.*3353G>T	ENSP00000463427.1:n.*3353G>T
ENST00000584450.5:c.*142G>T	ENSP00000463714.1:n.*142G>T
ENST00000584601.5:c.3473G>T	ENSP00000462438.1:p.Gly1158Val
NM_001005862.2:c.3473G>T , LRG_724t1:c.3473G>T	NP_001005862.1:p.Gly1158Val
NM_001289936.1:c.3518G>T , LRG_724t4:c.3518G>T	NP_001276865.1:p.Gly1173Val
NM_001289937.1:c.*142G>T	NP_001276866.1:n.*142G>T
NM_004448.3:c.3563G>T , LRG_724t2:c.3563G>T	NP_004439.2:p.Gly1188Val
NR_110535.1:n.3887G>T
XM_024450641.1:c.3701G>T	XP_024306409.1:p.Gly1234Val
XM_024450642.1:c.3656G>T	XP_024306410.1:p.Gly1219Val
XM_024450643.1:c.3611G>T	XP_024306411.1:p.Gly1204Val
NM_001005862.3:c.3473G>T	NP_001005862.1:p.Gly1158Val
NM_001289936.2:c.3518G>T	NP_001276865.1:p.Gly1173Val
NM_001289937.2:c.*142G>T	NP_001276866.1:n.*142G>T
NM_001382782.1:c.3473G>T	NP_001369711.1:p.Gly1158Val
NM_001382783.1:c.3473G>T	NP_001369712.1:p.Gly1158Val
NM_001382784.1:c.3680G>T	NP_001369713.1:p.Gly1227Val
NM_001382785.1:c.3665G>T	NP_001369714.1:p.Gly1222Val
NM_001382786.1:c.3644G>T	NP_001369715.1:p.Gly1215Val
NM_001382787.1:c.3638G>T	NP_001369716.1:p.Gly1213Val
NM_001382788.1:c.3593G>T	NP_001369717.1:p.Gly1198Val
NM_001382789.1:c.3584G>T	NP_001369718.1:p.Gly1195Val
NM_001382790.1:c.3560G>T	NP_001369719.1:p.Gly1187Val
NM_001382791.1:c.3554G>T	NP_001369720.1:p.Gly1185Val
NM_001382792.1:c.3527G>T	NP_001369721.1:p.Gly1176Val
NM_001382793.1:c.3521G>T	NP_001369722.1:p.Gly1174Val
NM_001382794.1:c.3521G>T	NP_001369723.1:p.Gly1174Val
NM_001382795.1:c.3515G>T	NP_001369724.1:p.Gly1172Val
NM_001382796.1:c.3476G>T	NP_001369725.1:p.Gly1159Val
NM_001382797.1:c.3464G>T	NP_001369726.1:p.Gly1155Val
NM_001382798.1:c.3407G>T	NP_001369727.1:p.Gly1136Val
NM_001382799.1:c.3383G>T	NP_001369728.1:p.Gly1128Val
NM_001382800.1:c.3377G>T	NP_001369729.1:p.Gly1126Val
NM_001382801.1:c.3359G>T	NP_001369730.1:p.Gly1120Val
NM_001382802.1:c.3305G>T	NP_001369731.1:p.Gly1102Val
NM_001382803.1:c.*142G>T	NP_001369732.1:n.*142G>T
NM_001382804.1:c.2735G>T	NP_001369733.1:p.Gly912Val
NM_001382805.1:c.2612G>T	NP_001369734.1:p.Gly871Val
NM_001382806.1:c.2525G>T	NP_001369735.1:p.Gly842Val
NM_004448.4:c.3563G>T MANE Select	NP_004439.2:p.Gly1188Val
NR_110535.2:n.3801G>T