Canonical Allele Identifier: CA399304738

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145865647
• COSMIC: COSM88803 ; COSM5363941
• MyVariant Identifiers: chr17:g.37881392A>G (hg19) ; chr17:g.39725139A>G (hg38)
• CIViC: CA399304738

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725139A>G , CM000679.2:g.39725139A>G	GRCh38
NC_000017.10:g.37881392A>G , CM000679.1:g.37881392A>G	GRCh37
NC_000017.9:g.35134918A>G	NCBI36
NG_007503.1:g.42000A>G , LRG_724:g.42000A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2584A>G MANE Select	ENSP00000269571.4:p.Thr862Ala
ENST00000269571.9:c.2584A>G	ENSP00000269571.4:p.Thr862Ala
ENST00000406381.6:c.2494A>G	ENSP00000385185.2:p.Thr832Ala
ENST00000445658.6:c.1756A>G	ENSP00000404047.2:p.Thr586Ala
ENST00000541774.5:c.2539A>G	ENSP00000446466.1:p.Thr847Ala
ENST00000578373.5:c.*2374A>G	ENSP00000463427.1:n.*2374A>G
ENST00000580074.1:c.690A>G
ENST00000583038.5:n.3718A>G
ENST00000584450.5:c.2584A>G	ENSP00000463714.1:p.Thr862Ala
ENST00000584601.5:c.2494A>G	ENSP00000462438.1:p.Thr832Ala
NM_001005862.2:c.2494A>G , LRG_724t1:c.2494A>G	NP_001005862.1:p.Thr832Ala
NM_001289936.1:c.2539A>G , LRG_724t4:c.2539A>G	NP_001276865.1:p.Thr847Ala
NM_001289937.1:c.2584A>G	NP_001276866.1:p.Thr862Ala
NM_004448.3:c.2584A>G , LRG_724t2:c.2584A>G	NP_004439.2:p.Thr862Ala
NR_110535.1:n.2908A>G
XM_024450641.1:c.2722A>G	XP_024306409.1:p.Thr908Ala
XM_024450642.1:c.2677A>G	XP_024306410.1:p.Thr893Ala
XM_024450643.1:c.2632A>G	XP_024306411.1:p.Thr878Ala
NM_001005862.3:c.2494A>G	NP_001005862.1:p.Thr832Ala
NM_001289936.2:c.2539A>G	NP_001276865.1:p.Thr847Ala
NM_001289937.2:c.2584A>G	NP_001276866.1:p.Thr862Ala
NM_001382782.1:c.2494A>G	NP_001369711.1:p.Thr832Ala
NM_001382783.1:c.2494A>G	NP_001369712.1:p.Thr832Ala
NM_001382784.1:c.2701A>G	NP_001369713.1:p.Thr901Ala
NM_001382785.1:c.2686A>G	NP_001369714.1:p.Thr896Ala
NM_001382786.1:c.2665A>G	NP_001369715.1:p.Thr889Ala
NM_001382787.1:c.2659A>G	NP_001369716.1:p.Thr887Ala
NM_001382788.1:c.2614A>G	NP_001369717.1:p.Thr872Ala
NM_001382789.1:c.2605A>G	NP_001369718.1:p.Thr869Ala
NM_001382790.1:c.2581A>G	NP_001369719.1:p.Thr861Ala
NM_001382791.1:c.2575A>G	NP_001369720.1:p.Thr859Ala
NM_001382792.1:c.2548A>G	NP_001369721.1:p.Thr850Ala
NM_001382793.1:c.2542A>G	NP_001369722.1:p.Thr848Ala
NM_001382794.1:c.2542A>G	NP_001369723.1:p.Thr848Ala
NM_001382795.1:c.2536A>G	NP_001369724.1:p.Thr846Ala
NM_001382796.1:c.2584A>G	NP_001369725.1:p.Thr862Ala
NM_001382797.1:c.2485A>G	NP_001369726.1:p.Thr829Ala
NM_001382798.1:c.2494-188A>G	NP_001369727.1:n.2494-188A>G
NM_001382799.1:c.2404A>G	NP_001369728.1:p.Thr802Ala
NM_001382800.1:c.2398A>G	NP_001369729.1:p.Thr800Ala
NM_001382801.1:c.2446-188A>G	NP_001369730.1:n.2446-188A>G
NM_001382802.1:c.2326A>G	NP_001369731.1:p.Thr776Ala
NM_001382803.1:c.2542A>G	NP_001369732.1:p.Thr848Ala
NM_001382804.1:c.1756A>G	NP_001369733.1:p.Thr586Ala
NM_001382805.1:c.2208+1479A>G	NP_001369734.1:n.2208+1479A>G
NM_001382806.1:c.1546A>G	NP_001369735.1:p.Thr516Ala
NM_004448.4:c.2584A>G MANE Select	NP_004439.2:p.Thr862Ala
NR_110535.2:n.2822A>G