Canonical Allele Identifier: CA399304333

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145863486
• MyVariant Identifiers: chr17:g.37881338A>G (hg19) ; chr17:g.39725085A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725085A>G , CM000679.2:g.39725085A>G	GRCh38
NC_000017.10:g.37881338A>G , CM000679.1:g.37881338A>G	GRCh37
NC_000017.9:g.35134864A>G	NCBI36
NG_007503.1:g.41946A>G , LRG_724:g.41946A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2530A>G MANE Select	ENSP00000269571.4:p.Arg844Gly
ENST00000269571.9:c.2530A>G	ENSP00000269571.4:p.Arg844Gly
ENST00000406381.6:c.2440A>G	ENSP00000385185.2:p.Arg814Gly
ENST00000445658.6:c.1702A>G	ENSP00000404047.2:p.Arg568Gly
ENST00000541774.5:c.2485A>G	ENSP00000446466.1:p.Arg829Gly
ENST00000578373.5:c.*2320A>G	ENSP00000463427.1:n.*2320A>G
ENST00000580074.1:c.636A>G
ENST00000583038.5:n.3664A>G
ENST00000584450.5:c.2530A>G	ENSP00000463714.1:p.Arg844Gly
ENST00000584601.5:c.2440A>G	ENSP00000462438.1:p.Arg814Gly
NM_001005862.2:c.2440A>G , LRG_724t1:c.2440A>G	NP_001005862.1:p.Arg814Gly
NM_001289936.1:c.2485A>G , LRG_724t4:c.2485A>G	NP_001276865.1:p.Arg829Gly
NM_001289937.1:c.2530A>G	NP_001276866.1:p.Arg844Gly
NM_004448.3:c.2530A>G , LRG_724t2:c.2530A>G	NP_004439.2:p.Arg844Gly
NR_110535.1:n.2854A>G
XM_024450641.1:c.2668A>G	XP_024306409.1:p.Arg890Gly
XM_024450642.1:c.2623A>G	XP_024306410.1:p.Arg875Gly
XM_024450643.1:c.2578A>G	XP_024306411.1:p.Arg860Gly
NM_001005862.3:c.2440A>G	NP_001005862.1:p.Arg814Gly
NM_001289936.2:c.2485A>G	NP_001276865.1:p.Arg829Gly
NM_001289937.2:c.2530A>G	NP_001276866.1:p.Arg844Gly
NM_001382782.1:c.2440A>G	NP_001369711.1:p.Arg814Gly
NM_001382783.1:c.2440A>G	NP_001369712.1:p.Arg814Gly
NM_001382784.1:c.2647A>G	NP_001369713.1:p.Arg883Gly
NM_001382785.1:c.2632A>G	NP_001369714.1:p.Arg878Gly
NM_001382786.1:c.2611A>G	NP_001369715.1:p.Arg871Gly
NM_001382787.1:c.2605A>G	NP_001369716.1:p.Arg869Gly
NM_001382788.1:c.2560A>G	NP_001369717.1:p.Arg854Gly
NM_001382789.1:c.2551A>G	NP_001369718.1:p.Arg851Gly
NM_001382790.1:c.2527A>G	NP_001369719.1:p.Arg843Gly
NM_001382791.1:c.2521A>G	NP_001369720.1:p.Arg841Gly
NM_001382792.1:c.2494A>G	NP_001369721.1:p.Arg832Gly
NM_001382793.1:c.2488A>G	NP_001369722.1:p.Arg830Gly
NM_001382794.1:c.2488A>G	NP_001369723.1:p.Arg830Gly
NM_001382795.1:c.2482A>G	NP_001369724.1:p.Arg828Gly
NM_001382796.1:c.2530A>G	NP_001369725.1:p.Arg844Gly
NM_001382797.1:c.2431A>G	NP_001369726.1:p.Arg811Gly
NM_001382798.1:c.2493+174A>G	NP_001369727.1:n.2493+174A>G
NM_001382799.1:c.2350A>G	NP_001369728.1:p.Arg784Gly
NM_001382800.1:c.2344A>G	NP_001369729.1:p.Arg782Gly
NM_001382801.1:c.2445+174A>G	NP_001369730.1:n.2445+174A>G
NM_001382802.1:c.2272A>G	NP_001369731.1:p.Arg758Gly
NM_001382803.1:c.2488A>G	NP_001369732.1:p.Arg830Gly
NM_001382804.1:c.1702A>G	NP_001369733.1:p.Arg568Gly
NM_001382805.1:c.2208+1425A>G	NP_001369734.1:n.2208+1425A>G
NM_001382806.1:c.1492A>G	NP_001369735.1:p.Arg498Gly
NM_004448.4:c.2530A>G MANE Select	NP_004439.2:p.Arg844Gly
NR_110535.2:n.2768A>G