Canonical Allele Identifier: CA399302901

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145848475
• COSMIC: COSM85895
• MyVariant Identifiers: chr17:g.37881013A>G (hg19) ; chr17:g.39724760A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724760A>G , CM000679.2:g.39724760A>G	GRCh38
NC_000017.10:g.37881013A>G , CM000679.1:g.37881013A>G	GRCh37
NC_000017.9:g.35134539A>G	NCBI36
NG_007503.1:g.41621A>G , LRG_724:g.41621A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2342A>G MANE Select	ENSP00000269571.4:p.Tyr781Cys
ENST00000269571.9:c.2342A>G	ENSP00000269571.4:p.Tyr781Cys
ENST00000406381.6:c.2252A>G	ENSP00000385185.2:p.Tyr751Cys
ENST00000445658.6:c.1514A>G	ENSP00000404047.2:p.Tyr505Cys
ENST00000541774.5:c.2297A>G	ENSP00000446466.1:p.Tyr766Cys
ENST00000578373.5:c.*2132A>G	ENSP00000463427.1:n.*2132A>G
ENST00000580074.1:c.448A>G
ENST00000583038.5:n.3476A>G
ENST00000584450.5:c.2342A>G	ENSP00000463714.1:p.Tyr781Cys
ENST00000584601.5:c.2252A>G	ENSP00000462438.1:p.Tyr751Cys
NM_001005862.2:c.2252A>G , LRG_724t1:c.2252A>G	NP_001005862.1:p.Tyr751Cys
NM_001289936.1:c.2297A>G , LRG_724t4:c.2297A>G	NP_001276865.1:p.Tyr766Cys
NM_001289937.1:c.2342A>G	NP_001276866.1:p.Tyr781Cys
NM_004448.3:c.2342A>G , LRG_724t2:c.2342A>G	NP_004439.2:p.Tyr781Cys
NR_110535.1:n.2666A>G
XM_024450641.1:c.2480A>G	XP_024306409.1:p.Tyr827Cys
XM_024450642.1:c.2435A>G	XP_024306410.1:p.Tyr812Cys
XM_024450643.1:c.2390A>G	XP_024306411.1:p.Tyr797Cys
NM_001005862.3:c.2252A>G	NP_001005862.1:p.Tyr751Cys
NM_001289936.2:c.2297A>G	NP_001276865.1:p.Tyr766Cys
NM_001289937.2:c.2342A>G	NP_001276866.1:p.Tyr781Cys
NM_001382782.1:c.2252A>G	NP_001369711.1:p.Tyr751Cys
NM_001382783.1:c.2252A>G	NP_001369712.1:p.Tyr751Cys
NM_001382784.1:c.2459A>G	NP_001369713.1:p.Tyr820Cys
NM_001382785.1:c.2444A>G	NP_001369714.1:p.Tyr815Cys
NM_001382786.1:c.2423A>G	NP_001369715.1:p.Tyr808Cys
NM_001382787.1:c.2417A>G	NP_001369716.1:p.Tyr806Cys
NM_001382788.1:c.2372A>G	NP_001369717.1:p.Tyr791Cys
NM_001382789.1:c.2363A>G	NP_001369718.1:p.Tyr788Cys
NM_001382790.1:c.2339A>G	NP_001369719.1:p.Tyr780Cys
NM_001382791.1:c.2333A>G	NP_001369720.1:p.Tyr778Cys
NM_001382792.1:c.2306A>G	NP_001369721.1:p.Tyr769Cys
NM_001382793.1:c.2300A>G	NP_001369722.1:p.Tyr767Cys
NM_001382794.1:c.2300A>G	NP_001369723.1:p.Tyr767Cys
NM_001382795.1:c.2294A>G	NP_001369724.1:p.Tyr765Cys
NM_001382796.1:c.2342A>G	NP_001369725.1:p.Tyr781Cys
NM_001382797.1:c.2243A>G	NP_001369726.1:p.Tyr748Cys
NM_001382798.1:c.2342A>G	NP_001369727.1:p.Tyr781Cys
NM_001382799.1:c.2162A>G	NP_001369728.1:p.Tyr721Cys
NM_001382800.1:c.2308-289A>G	NP_001369729.1:n.2308-289A>G
NM_001382801.1:c.2294A>G	NP_001369730.1:p.Tyr765Cys
NM_001382802.1:c.2084A>G	NP_001369731.1:p.Tyr695Cys
NM_001382803.1:c.2300A>G	NP_001369732.1:p.Tyr767Cys
NM_001382804.1:c.1514A>G	NP_001369733.1:p.Tyr505Cys
NM_001382805.1:c.2208+1100A>G	NP_001369734.1:n.2208+1100A>G
NM_001382806.1:c.1304A>G	NP_001369735.1:p.Tyr435Cys
NM_004448.4:c.2342A>G MANE Select	NP_004439.2:p.Tyr781Cys
NR_110535.2:n.2580A>G