Canonical Allele Identifier: CA269884

Gene: ERBB2

Linked Data

• ClinVar Variation Id: 133279
• ClinVar RCV Id: RCV000119789
• dbSNP Id: rs137852788
• MyVariant Identifiers: chr17:g.37881343C>T (hg19) ; chr17:g.39725090C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2535C>T MANE Select	ENSP00000269571.4:p.Asp845=
ENST00000269571.9:c.2535C>T	ENSP00000269571.4:p.Asp845=
ENST00000406381.6:c.2445C>T	ENSP00000385185.2:p.Asp815=
ENST00000445658.6:c.1707C>T	ENSP00000404047.2:p.Asp569=
ENST00000541774.5:c.2490C>T	ENSP00000446466.1:p.Asp830=
ENST00000578373.5:c.*2325C>T	ENSP00000463427.1:n.*2325C>T
ENST00000580074.1:c.641C>T
ENST00000583038.5:n.3669C>T
ENST00000584450.5:c.2535C>T	ENSP00000463714.1:p.Asp845=
ENST00000584601.5:c.2445C>T	ENSP00000462438.1:p.Asp815=
NM_001005862.2:c.2445C>T , LRG_724t1:c.2445C>T	NP_001005862.1:p.Asp815=
NM_001289936.1:c.2490C>T , LRG_724t4:c.2490C>T	NP_001276865.1:p.Asp830=
NM_001289937.1:c.2535C>T	NP_001276866.1:p.Asp845=
NM_004448.3:c.2535C>T , LRG_724t2:c.2535C>T	NP_004439.2:p.Asp845=
NR_110535.1:n.2859C>T
XM_024450641.1:c.2673C>T	XP_024306409.1:p.Asp891=
XM_024450642.1:c.2628C>T	XP_024306410.1:p.Asp876=
XM_024450643.1:c.2583C>T	XP_024306411.1:p.Asp861=
NM_001005862.3:c.2445C>T	NP_001005862.1:p.Asp815=
NM_001289936.2:c.2490C>T	NP_001276865.1:p.Asp830=
NM_001289937.2:c.2535C>T	NP_001276866.1:p.Asp845=
NM_001382782.1:c.2445C>T	NP_001369711.1:p.Asp815=
NM_001382783.1:c.2445C>T	NP_001369712.1:p.Asp815=
NM_001382784.1:c.2652C>T	NP_001369713.1:p.Asp884=
NM_001382785.1:c.2637C>T	NP_001369714.1:p.Asp879=
NM_001382786.1:c.2616C>T	NP_001369715.1:p.Asp872=
NM_001382787.1:c.2610C>T	NP_001369716.1:p.Asp870=
NM_001382788.1:c.2565C>T	NP_001369717.1:p.Asp855=
NM_001382789.1:c.2556C>T	NP_001369718.1:p.Asp852=
NM_001382790.1:c.2532C>T	NP_001369719.1:p.Asp844=
NM_001382791.1:c.2526C>T	NP_001369720.1:p.Asp842=
NM_001382792.1:c.2499C>T	NP_001369721.1:p.Asp833=
NM_001382793.1:c.2493C>T	NP_001369722.1:p.Asp831=
NM_001382794.1:c.2493C>T	NP_001369723.1:p.Asp831=
NM_001382795.1:c.2487C>T	NP_001369724.1:p.Asp829=
NM_001382796.1:c.2535C>T	NP_001369725.1:p.Asp845=
NM_001382797.1:c.2436C>T	NP_001369726.1:p.Asp812=
NM_001382798.1:c.2493+179C>T	NP_001369727.1:n.2493+179C>T
NM_001382799.1:c.2355C>T	NP_001369728.1:p.Asp785=
NM_001382800.1:c.2349C>T	NP_001369729.1:p.Asp783=
NM_001382801.1:c.2445+179C>T	NP_001369730.1:n.2445+179C>T
NM_001382802.1:c.2277C>T	NP_001369731.1:p.Asp759=
NM_001382803.1:c.2493C>T	NP_001369732.1:p.Asp831=
NM_001382804.1:c.1707C>T	NP_001369733.1:p.Asp569=
NM_001382805.1:c.2208+1430C>T	NP_001369734.1:n.2208+1430C>T
NM_001382806.1:c.1497C>T	NP_001369735.1:p.Asp499=
NM_004448.4:c.2535C>T MANE Select	NP_004439.2:p.Asp845=
NR_110535.2:n.2773C>T