Canonical Allele Identifier: CA399304438

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145864282
• MyVariant Identifiers: chr17:g.37881356A>T (hg19) ; chr17:g.39725103A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725103A>T , CM000679.2:g.39725103A>T	GRCh38
NC_000017.10:g.37881356A>T , CM000679.1:g.37881356A>T	GRCh37
NC_000017.9:g.35134882A>T	NCBI36
NG_007503.1:g.41964A>T , LRG_724:g.41964A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2548A>T MANE Select	ENSP00000269571.4:p.Asn850Tyr
ENST00000269571.9:c.2548A>T	ENSP00000269571.4:p.Asn850Tyr
ENST00000406381.6:c.2458A>T	ENSP00000385185.2:p.Asn820Tyr
ENST00000445658.6:c.1720A>T	ENSP00000404047.2:p.Asn574Tyr
ENST00000541774.5:c.2503A>T	ENSP00000446466.1:p.Asn835Tyr
ENST00000578373.5:c.*2338A>T	ENSP00000463427.1:n.*2338A>T
ENST00000580074.1:c.654A>T
ENST00000583038.5:n.3682A>T
ENST00000584450.5:c.2548A>T	ENSP00000463714.1:p.Asn850Tyr
ENST00000584601.5:c.2458A>T	ENSP00000462438.1:p.Asn820Tyr
NM_001005862.2:c.2458A>T , LRG_724t1:c.2458A>T	NP_001005862.1:p.Asn820Tyr
NM_001289936.1:c.2503A>T , LRG_724t4:c.2503A>T	NP_001276865.1:p.Asn835Tyr
NM_001289937.1:c.2548A>T	NP_001276866.1:p.Asn850Tyr
NM_004448.3:c.2548A>T , LRG_724t2:c.2548A>T	NP_004439.2:p.Asn850Tyr
NR_110535.1:n.2872A>T
XM_024450641.1:c.2686A>T	XP_024306409.1:p.Asn896Tyr
XM_024450642.1:c.2641A>T	XP_024306410.1:p.Asn881Tyr
XM_024450643.1:c.2596A>T	XP_024306411.1:p.Asn866Tyr
NM_001005862.3:c.2458A>T	NP_001005862.1:p.Asn820Tyr
NM_001289936.2:c.2503A>T	NP_001276865.1:p.Asn835Tyr
NM_001289937.2:c.2548A>T	NP_001276866.1:p.Asn850Tyr
NM_001382782.1:c.2458A>T	NP_001369711.1:p.Asn820Tyr
NM_001382783.1:c.2458A>T	NP_001369712.1:p.Asn820Tyr
NM_001382784.1:c.2665A>T	NP_001369713.1:p.Asn889Tyr
NM_001382785.1:c.2650A>T	NP_001369714.1:p.Asn884Tyr
NM_001382786.1:c.2629A>T	NP_001369715.1:p.Asn877Tyr
NM_001382787.1:c.2623A>T	NP_001369716.1:p.Asn875Tyr
NM_001382788.1:c.2578A>T	NP_001369717.1:p.Asn860Tyr
NM_001382789.1:c.2569A>T	NP_001369718.1:p.Asn857Tyr
NM_001382790.1:c.2545A>T	NP_001369719.1:p.Asn849Tyr
NM_001382791.1:c.2539A>T	NP_001369720.1:p.Asn847Tyr
NM_001382792.1:c.2512A>T	NP_001369721.1:p.Asn838Tyr
NM_001382793.1:c.2506A>T	NP_001369722.1:p.Asn836Tyr
NM_001382794.1:c.2506A>T	NP_001369723.1:p.Asn836Tyr
NM_001382795.1:c.2500A>T	NP_001369724.1:p.Asn834Tyr
NM_001382796.1:c.2548A>T	NP_001369725.1:p.Asn850Tyr
NM_001382797.1:c.2449A>T	NP_001369726.1:p.Asn817Tyr
NM_001382798.1:c.2493+192A>T	NP_001369727.1:n.2493+192A>T
NM_001382799.1:c.2368A>T	NP_001369728.1:p.Asn790Tyr
NM_001382800.1:c.2362A>T	NP_001369729.1:p.Asn788Tyr
NM_001382801.1:c.2445+192A>T	NP_001369730.1:n.2445+192A>T
NM_001382802.1:c.2290A>T	NP_001369731.1:p.Asn764Tyr
NM_001382803.1:c.2506A>T	NP_001369732.1:p.Asn836Tyr
NM_001382804.1:c.1720A>T	NP_001369733.1:p.Asn574Tyr
NM_001382805.1:c.2208+1443A>T	NP_001369734.1:n.2208+1443A>T
NM_001382806.1:c.1510A>T	NP_001369735.1:p.Asn504Tyr
NM_004448.4:c.2548A>T MANE Select	NP_004439.2:p.Asn850Tyr
NR_110535.2:n.2786A>T