Canonical Allele Identifier: CA399304377

Gene: ERBB2

Linked Data

• dbSNP Id: rs137852788
• gnomAD v4: 17-39725090-C-G
• MyVariant Identifiers: chr17:g.37881343C>G (hg19) ; chr17:g.39725090C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725090C>G , CM000679.2:g.39725090C>G	GRCh38
NC_000017.10:g.37881343C>G , CM000679.1:g.37881343C>G	GRCh37
NC_000017.9:g.35134869C>G	NCBI36
NG_007503.1:g.41951C>G , LRG_724:g.41951C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2535C>G MANE Select	ENSP00000269571.4:p.Asp845Glu
ENST00000269571.9:c.2535C>G	ENSP00000269571.4:p.Asp845Glu
ENST00000406381.6:c.2445C>G	ENSP00000385185.2:p.Asp815Glu
ENST00000445658.6:c.1707C>G	ENSP00000404047.2:p.Asp569Glu
ENST00000541774.5:c.2490C>G	ENSP00000446466.1:p.Asp830Glu
ENST00000578373.5:c.*2325C>G	ENSP00000463427.1:n.*2325C>G
ENST00000580074.1:c.641C>G
ENST00000583038.5:n.3669C>G
ENST00000584450.5:c.2535C>G	ENSP00000463714.1:p.Asp845Glu
ENST00000584601.5:c.2445C>G	ENSP00000462438.1:p.Asp815Glu
NM_001005862.2:c.2445C>G , LRG_724t1:c.2445C>G	NP_001005862.1:p.Asp815Glu
NM_001289936.1:c.2490C>G , LRG_724t4:c.2490C>G	NP_001276865.1:p.Asp830Glu
NM_001289937.1:c.2535C>G	NP_001276866.1:p.Asp845Glu
NM_004448.3:c.2535C>G , LRG_724t2:c.2535C>G	NP_004439.2:p.Asp845Glu
NR_110535.1:n.2859C>G
XM_024450641.1:c.2673C>G	XP_024306409.1:p.Asp891Glu
XM_024450642.1:c.2628C>G	XP_024306410.1:p.Asp876Glu
XM_024450643.1:c.2583C>G	XP_024306411.1:p.Asp861Glu
NM_001005862.3:c.2445C>G	NP_001005862.1:p.Asp815Glu
NM_001289936.2:c.2490C>G	NP_001276865.1:p.Asp830Glu
NM_001289937.2:c.2535C>G	NP_001276866.1:p.Asp845Glu
NM_001382782.1:c.2445C>G	NP_001369711.1:p.Asp815Glu
NM_001382783.1:c.2445C>G	NP_001369712.1:p.Asp815Glu
NM_001382784.1:c.2652C>G	NP_001369713.1:p.Asp884Glu
NM_001382785.1:c.2637C>G	NP_001369714.1:p.Asp879Glu
NM_001382786.1:c.2616C>G	NP_001369715.1:p.Asp872Glu
NM_001382787.1:c.2610C>G	NP_001369716.1:p.Asp870Glu
NM_001382788.1:c.2565C>G	NP_001369717.1:p.Asp855Glu
NM_001382789.1:c.2556C>G	NP_001369718.1:p.Asp852Glu
NM_001382790.1:c.2532C>G	NP_001369719.1:p.Asp844Glu
NM_001382791.1:c.2526C>G	NP_001369720.1:p.Asp842Glu
NM_001382792.1:c.2499C>G	NP_001369721.1:p.Asp833Glu
NM_001382793.1:c.2493C>G	NP_001369722.1:p.Asp831Glu
NM_001382794.1:c.2493C>G	NP_001369723.1:p.Asp831Glu
NM_001382795.1:c.2487C>G	NP_001369724.1:p.Asp829Glu
NM_001382796.1:c.2535C>G	NP_001369725.1:p.Asp845Glu
NM_001382797.1:c.2436C>G	NP_001369726.1:p.Asp812Glu
NM_001382798.1:c.2493+179C>G	NP_001369727.1:n.2493+179C>G
NM_001382799.1:c.2355C>G	NP_001369728.1:p.Asp785Glu
NM_001382800.1:c.2349C>G	NP_001369729.1:p.Asp783Glu
NM_001382801.1:c.2445+179C>G	NP_001369730.1:n.2445+179C>G
NM_001382802.1:c.2277C>G	NP_001369731.1:p.Asp759Glu
NM_001382803.1:c.2493C>G	NP_001369732.1:p.Asp831Glu
NM_001382804.1:c.1707C>G	NP_001369733.1:p.Asp569Glu
NM_001382805.1:c.2208+1430C>G	NP_001369734.1:n.2208+1430C>G
NM_001382806.1:c.1497C>G	NP_001369735.1:p.Asp499Glu
NM_004448.4:c.2535C>G MANE Select	NP_004439.2:p.Asp845Glu
NR_110535.2:n.2773C>G