Canonical Allele Identifier: CA399303013

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849122
• gnomAD v4: 17-39724778-G-T
• MyVariant Identifiers: chr17:g.37881031G>T (hg19) ; chr17:g.39724778G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724778G>T , CM000679.2:g.39724778G>T	GRCh38
NC_000017.10:g.37881031G>T , CM000679.1:g.37881031G>T	GRCh37
NC_000017.9:g.35134557G>T	NCBI36
NG_007503.1:g.41639G>T , LRG_724:g.41639G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2360G>T MANE Select	ENSP00000269571.4:p.Gly787Val
ENST00000269571.9:c.2360G>T	ENSP00000269571.4:p.Gly787Val
ENST00000406381.6:c.2270G>T	ENSP00000385185.2:p.Gly757Val
ENST00000445658.6:c.1532G>T	ENSP00000404047.2:p.Gly511Val
ENST00000541774.5:c.2315G>T	ENSP00000446466.1:p.Gly772Val
ENST00000578373.5:c.*2150G>T	ENSP00000463427.1:n.*2150G>T
ENST00000580074.1:c.466G>T
ENST00000583038.5:n.3494G>T
ENST00000584450.5:c.2360G>T	ENSP00000463714.1:p.Gly787Val
ENST00000584601.5:c.2270G>T	ENSP00000462438.1:p.Gly757Val
NM_001005862.2:c.2270G>T , LRG_724t1:c.2270G>T	NP_001005862.1:p.Gly757Val
NM_001289936.1:c.2315G>T , LRG_724t4:c.2315G>T	NP_001276865.1:p.Gly772Val
NM_001289937.1:c.2360G>T	NP_001276866.1:p.Gly787Val
NM_004448.3:c.2360G>T , LRG_724t2:c.2360G>T	NP_004439.2:p.Gly787Val
NR_110535.1:n.2684G>T
XM_024450641.1:c.2498G>T	XP_024306409.1:p.Gly833Val
XM_024450642.1:c.2453G>T	XP_024306410.1:p.Gly818Val
XM_024450643.1:c.2408G>T	XP_024306411.1:p.Gly803Val
NM_001005862.3:c.2270G>T	NP_001005862.1:p.Gly757Val
NM_001289936.2:c.2315G>T	NP_001276865.1:p.Gly772Val
NM_001289937.2:c.2360G>T	NP_001276866.1:p.Gly787Val
NM_001382782.1:c.2270G>T	NP_001369711.1:p.Gly757Val
NM_001382783.1:c.2270G>T	NP_001369712.1:p.Gly757Val
NM_001382784.1:c.2477G>T	NP_001369713.1:p.Gly826Val
NM_001382785.1:c.2462G>T	NP_001369714.1:p.Gly821Val
NM_001382786.1:c.2441G>T	NP_001369715.1:p.Gly814Val
NM_001382787.1:c.2435G>T	NP_001369716.1:p.Gly812Val
NM_001382788.1:c.2390G>T	NP_001369717.1:p.Gly797Val
NM_001382789.1:c.2381G>T	NP_001369718.1:p.Gly794Val
NM_001382790.1:c.2357G>T	NP_001369719.1:p.Gly786Val
NM_001382791.1:c.2351G>T	NP_001369720.1:p.Gly784Val
NM_001382792.1:c.2324G>T	NP_001369721.1:p.Gly775Val
NM_001382793.1:c.2318G>T	NP_001369722.1:p.Gly773Val
NM_001382794.1:c.2318G>T	NP_001369723.1:p.Gly773Val
NM_001382795.1:c.2312G>T	NP_001369724.1:p.Gly771Val
NM_001382796.1:c.2360G>T	NP_001369725.1:p.Gly787Val
NM_001382797.1:c.2261G>T	NP_001369726.1:p.Gly754Val
NM_001382798.1:c.2360G>T	NP_001369727.1:p.Gly787Val
NM_001382799.1:c.2180G>T	NP_001369728.1:p.Gly727Val
NM_001382800.1:c.2308-271G>T	NP_001369729.1:n.2308-271G>T
NM_001382801.1:c.2312G>T	NP_001369730.1:p.Gly771Val
NM_001382802.1:c.2102G>T	NP_001369731.1:p.Gly701Val
NM_001382803.1:c.2318G>T	NP_001369732.1:p.Gly773Val
NM_001382804.1:c.1532G>T	NP_001369733.1:p.Gly511Val
NM_001382805.1:c.2208+1118G>T	NP_001369734.1:n.2208+1118G>T
NM_001382806.1:c.1322G>T	NP_001369735.1:p.Gly441Val
NM_004448.4:c.2360G>T MANE Select	NP_004439.2:p.Gly787Val
NR_110535.2:n.2598G>T