Canonical Allele Identifier: CA399304441

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145864310
• MyVariant Identifiers: chr17:g.37881357A>C (hg19) ; chr17:g.39725104A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725104A>C , CM000679.2:g.39725104A>C	GRCh38
NC_000017.10:g.37881357A>C , CM000679.1:g.37881357A>C	GRCh37
NC_000017.9:g.35134883A>C	NCBI36
NG_007503.1:g.41965A>C , LRG_724:g.41965A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2549A>C MANE Select	ENSP00000269571.4:p.Asn850Thr
ENST00000269571.9:c.2549A>C	ENSP00000269571.4:p.Asn850Thr
ENST00000406381.6:c.2459A>C	ENSP00000385185.2:p.Asn820Thr
ENST00000445658.6:c.1721A>C	ENSP00000404047.2:p.Asn574Thr
ENST00000541774.5:c.2504A>C	ENSP00000446466.1:p.Asn835Thr
ENST00000578373.5:c.*2339A>C	ENSP00000463427.1:n.*2339A>C
ENST00000580074.1:c.655A>C
ENST00000583038.5:n.3683A>C
ENST00000584450.5:c.2549A>C	ENSP00000463714.1:p.Asn850Thr
ENST00000584601.5:c.2459A>C	ENSP00000462438.1:p.Asn820Thr
NM_001005862.2:c.2459A>C , LRG_724t1:c.2459A>C	NP_001005862.1:p.Asn820Thr
NM_001289936.1:c.2504A>C , LRG_724t4:c.2504A>C	NP_001276865.1:p.Asn835Thr
NM_001289937.1:c.2549A>C	NP_001276866.1:p.Asn850Thr
NM_004448.3:c.2549A>C , LRG_724t2:c.2549A>C	NP_004439.2:p.Asn850Thr
NR_110535.1:n.2873A>C
XM_024450641.1:c.2687A>C	XP_024306409.1:p.Asn896Thr
XM_024450642.1:c.2642A>C	XP_024306410.1:p.Asn881Thr
XM_024450643.1:c.2597A>C	XP_024306411.1:p.Asn866Thr
NM_001005862.3:c.2459A>C	NP_001005862.1:p.Asn820Thr
NM_001289936.2:c.2504A>C	NP_001276865.1:p.Asn835Thr
NM_001289937.2:c.2549A>C	NP_001276866.1:p.Asn850Thr
NM_001382782.1:c.2459A>C	NP_001369711.1:p.Asn820Thr
NM_001382783.1:c.2459A>C	NP_001369712.1:p.Asn820Thr
NM_001382784.1:c.2666A>C	NP_001369713.1:p.Asn889Thr
NM_001382785.1:c.2651A>C	NP_001369714.1:p.Asn884Thr
NM_001382786.1:c.2630A>C	NP_001369715.1:p.Asn877Thr
NM_001382787.1:c.2624A>C	NP_001369716.1:p.Asn875Thr
NM_001382788.1:c.2579A>C	NP_001369717.1:p.Asn860Thr
NM_001382789.1:c.2570A>C	NP_001369718.1:p.Asn857Thr
NM_001382790.1:c.2546A>C	NP_001369719.1:p.Asn849Thr
NM_001382791.1:c.2540A>C	NP_001369720.1:p.Asn847Thr
NM_001382792.1:c.2513A>C	NP_001369721.1:p.Asn838Thr
NM_001382793.1:c.2507A>C	NP_001369722.1:p.Asn836Thr
NM_001382794.1:c.2507A>C	NP_001369723.1:p.Asn836Thr
NM_001382795.1:c.2501A>C	NP_001369724.1:p.Asn834Thr
NM_001382796.1:c.2549A>C	NP_001369725.1:p.Asn850Thr
NM_001382797.1:c.2450A>C	NP_001369726.1:p.Asn817Thr
NM_001382798.1:c.2493+193A>C	NP_001369727.1:n.2493+193A>C
NM_001382799.1:c.2369A>C	NP_001369728.1:p.Asn790Thr
NM_001382800.1:c.2363A>C	NP_001369729.1:p.Asn788Thr
NM_001382801.1:c.2445+193A>C	NP_001369730.1:n.2445+193A>C
NM_001382802.1:c.2291A>C	NP_001369731.1:p.Asn764Thr
NM_001382803.1:c.2507A>C	NP_001369732.1:p.Asn836Thr
NM_001382804.1:c.1721A>C	NP_001369733.1:p.Asn574Thr
NM_001382805.1:c.2208+1444A>C	NP_001369734.1:n.2208+1444A>C
NM_001382806.1:c.1511A>C	NP_001369735.1:p.Asn504Thr
NM_004448.4:c.2549A>C MANE Select	NP_004439.2:p.Asn850Thr
NR_110535.2:n.2787A>C