Canonical Allele Identifier: CA499670897

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145850557
• MyVariant Identifiers: chr17:g.37881068G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724815G>A , CM000679.2:g.39724815G>A	GRCh38
NC_000017.10:g.37881068G>A , CM000679.1:g.37881068G>A	GRCh37
NC_000017.9:g.35134594G>A	NCBI36
NG_007503.1:g.41676G>A , LRG_724:g.41676G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2397G>A MANE Select	ENSP00000269571.4:p.Gln799=
ENST00000269571.9:c.2397G>A	ENSP00000269571.4:p.Gln799=
ENST00000406381.6:c.2307G>A	ENSP00000385185.2:p.Gln769=
ENST00000445658.6:c.1569G>A	ENSP00000404047.2:p.Gln523=
ENST00000541774.5:c.2352G>A	ENSP00000446466.1:p.Gln784=
ENST00000578373.5:c.*2187G>A	ENSP00000463427.1:n.*2187G>A
ENST00000580074.1:c.503G>A
ENST00000583038.5:n.3531G>A
ENST00000584450.5:c.2397G>A	ENSP00000463714.1:p.Gln799=
ENST00000584601.5:c.2307G>A	ENSP00000462438.1:p.Gln769=
NM_001005862.2:c.2307G>A , LRG_724t1:c.2307G>A	NP_001005862.1:p.Gln769=
NM_001289936.1:c.2352G>A , LRG_724t4:c.2352G>A	NP_001276865.1:p.Gln784=
NM_001289937.1:c.2397G>A	NP_001276866.1:p.Gln799=
NM_004448.3:c.2397G>A , LRG_724t2:c.2397G>A	NP_004439.2:p.Gln799=
NR_110535.1:n.2721G>A
XM_024450641.1:c.2535G>A	XP_024306409.1:p.Gln845=
XM_024450642.1:c.2490G>A	XP_024306410.1:p.Gln830=
XM_024450643.1:c.2445G>A	XP_024306411.1:p.Gln815=
NM_001005862.3:c.2307G>A	NP_001005862.1:p.Gln769=
NM_001289936.2:c.2352G>A	NP_001276865.1:p.Gln784=
NM_001289937.2:c.2397G>A	NP_001276866.1:p.Gln799=
NM_001382782.1:c.2307G>A	NP_001369711.1:p.Gln769=
NM_001382783.1:c.2307G>A	NP_001369712.1:p.Gln769=
NM_001382784.1:c.2514G>A	NP_001369713.1:p.Gln838=
NM_001382785.1:c.2499G>A	NP_001369714.1:p.Gln833=
NM_001382786.1:c.2478G>A	NP_001369715.1:p.Gln826=
NM_001382787.1:c.2472G>A	NP_001369716.1:p.Gln824=
NM_001382788.1:c.2427G>A	NP_001369717.1:p.Gln809=
NM_001382789.1:c.2418G>A	NP_001369718.1:p.Gln806=
NM_001382790.1:c.2394G>A	NP_001369719.1:p.Gln798=
NM_001382791.1:c.2388G>A	NP_001369720.1:p.Gln796=
NM_001382792.1:c.2361G>A	NP_001369721.1:p.Gln787=
NM_001382793.1:c.2355G>A	NP_001369722.1:p.Gln785=
NM_001382794.1:c.2355G>A	NP_001369723.1:p.Gln785=
NM_001382795.1:c.2349G>A	NP_001369724.1:p.Gln783=
NM_001382796.1:c.2397G>A	NP_001369725.1:p.Gln799=
NM_001382797.1:c.2298G>A	NP_001369726.1:p.Gln766=
NM_001382798.1:c.2397G>A	NP_001369727.1:p.Gln799=
NM_001382799.1:c.2217G>A	NP_001369728.1:p.Gln739=
NM_001382800.1:c.2308-234G>A	NP_001369729.1:n.2308-234G>A
NM_001382801.1:c.2349G>A	NP_001369730.1:p.Gln783=
NM_001382802.1:c.2139G>A	NP_001369731.1:p.Gln713=
NM_001382803.1:c.2355G>A	NP_001369732.1:p.Gln785=
NM_001382804.1:c.1569G>A	NP_001369733.1:p.Gln523=
NM_001382805.1:c.2208+1155G>A	NP_001369734.1:n.2208+1155G>A
NM_001382806.1:c.1359G>A	NP_001369735.1:p.Gln453=
NM_004448.4:c.2397G>A MANE Select	NP_004439.2:p.Gln799=
NR_110535.2:n.2635G>A