Canonical Allele Identifier: CA399310747

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37883677G>T (hg19) ; chr17:g.39727424G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727424G>T , CM000679.2:g.39727424G>T	GRCh38
NC_000017.10:g.37883677G>T , CM000679.1:g.37883677G>T	GRCh37
NC_000017.9:g.35137203G>T	NCBI36
NG_007503.1:g.44285G>T , LRG_724:g.44285G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3289G>T MANE Select	ENSP00000269571.4:p.Gly1097Trp
ENST00000269571.9:c.3289G>T	ENSP00000269571.4:p.Gly1097Trp
ENST00000406381.6:c.3199G>T	ENSP00000385185.2:p.Gly1067Trp
ENST00000445658.6:c.2461G>T	ENSP00000404047.2:p.Gly821Trp
ENST00000541774.5:c.3244G>T	ENSP00000446466.1:p.Gly1082Trp
ENST00000578373.5:c.*3079G>T	ENSP00000463427.1:n.*3079G>T
ENST00000584450.5:c.3160-265G>T	ENSP00000463714.1:n.3160-265G>T
ENST00000584601.5:c.3199G>T	ENSP00000462438.1:p.Gly1067Trp
NM_001005862.2:c.3199G>T , LRG_724t1:c.3199G>T	NP_001005862.1:p.Gly1067Trp
NM_001289936.1:c.3244G>T , LRG_724t4:c.3244G>T	NP_001276865.1:p.Gly1082Trp
NM_001289937.1:c.3160-265G>T	NP_001276866.1:n.3160-265G>T
NM_004448.3:c.3289G>T , LRG_724t2:c.3289G>T	NP_004439.2:p.Gly1097Trp
NR_110535.1:n.3613G>T
XM_024450641.1:c.3427G>T	XP_024306409.1:p.Gly1143Trp
XM_024450642.1:c.3382G>T	XP_024306410.1:p.Gly1128Trp
XM_024450643.1:c.3337G>T	XP_024306411.1:p.Gly1113Trp
NM_001005862.3:c.3199G>T	NP_001005862.1:p.Gly1067Trp
NM_001289936.2:c.3244G>T	NP_001276865.1:p.Gly1082Trp
NM_001289937.2:c.3160-265G>T	NP_001276866.1:n.3160-265G>T
NM_001382782.1:c.3199G>T	NP_001369711.1:p.Gly1067Trp
NM_001382783.1:c.3199G>T	NP_001369712.1:p.Gly1067Trp
NM_001382784.1:c.3406G>T	NP_001369713.1:p.Gly1136Trp
NM_001382785.1:c.3391G>T	NP_001369714.1:p.Gly1131Trp
NM_001382786.1:c.3370G>T	NP_001369715.1:p.Gly1124Trp
NM_001382787.1:c.3364G>T	NP_001369716.1:p.Gly1122Trp
NM_001382788.1:c.3319G>T	NP_001369717.1:p.Gly1107Trp
NM_001382789.1:c.3310G>T	NP_001369718.1:p.Gly1104Trp
NM_001382790.1:c.3286G>T	NP_001369719.1:p.Gly1096Trp
NM_001382791.1:c.3280G>T	NP_001369720.1:p.Gly1094Trp
NM_001382792.1:c.3253G>T	NP_001369721.1:p.Gly1085Trp
NM_001382793.1:c.3247G>T	NP_001369722.1:p.Gly1083Trp
NM_001382794.1:c.3247G>T	NP_001369723.1:p.Gly1083Trp
NM_001382795.1:c.3241G>T	NP_001369724.1:p.Gly1081Trp
NM_001382796.1:c.3202G>T	NP_001369725.1:p.Gly1068Trp
NM_001382797.1:c.3190G>T	NP_001369726.1:p.Gly1064Trp
NM_001382798.1:c.3133G>T	NP_001369727.1:p.Gly1045Trp
NM_001382799.1:c.3109G>T	NP_001369728.1:p.Gly1037Trp
NM_001382800.1:c.3103G>T	NP_001369729.1:p.Gly1035Trp
NM_001382801.1:c.3085G>T	NP_001369730.1:p.Gly1029Trp
NM_001382802.1:c.3031G>T	NP_001369731.1:p.Gly1011Trp
NM_001382803.1:c.3118-265G>T	NP_001369732.1:n.3118-265G>T
NM_001382804.1:c.2461G>T	NP_001369733.1:p.Gly821Trp
NM_001382805.1:c.2338G>T	NP_001369734.1:p.Gly780Trp
NM_001382806.1:c.2251G>T	NP_001369735.1:p.Gly751Trp
NM_004448.4:c.3289G>T MANE Select	NP_004439.2:p.Gly1097Trp
NR_110535.2:n.3527G>T