Canonical Allele Identifier: CA399304560

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881369A>C (hg19) ; chr17:g.39725116A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725116A>C , CM000679.2:g.39725116A>C	GRCh38
NC_000017.10:g.37881369A>C , CM000679.1:g.37881369A>C	GRCh37
NC_000017.9:g.35134895A>C	NCBI36
NG_007503.1:g.41977A>C , LRG_724:g.41977A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2561A>C MANE Select	ENSP00000269571.4:p.Lys854Thr
ENST00000269571.9:c.2561A>C	ENSP00000269571.4:p.Lys854Thr
ENST00000406381.6:c.2471A>C	ENSP00000385185.2:p.Lys824Thr
ENST00000445658.6:c.1733A>C	ENSP00000404047.2:p.Lys578Thr
ENST00000541774.5:c.2516A>C	ENSP00000446466.1:p.Lys839Thr
ENST00000578373.5:c.*2351A>C	ENSP00000463427.1:n.*2351A>C
ENST00000580074.1:c.667A>C
ENST00000583038.5:n.3695A>C
ENST00000584450.5:c.2561A>C	ENSP00000463714.1:p.Lys854Thr
ENST00000584601.5:c.2471A>C	ENSP00000462438.1:p.Lys824Thr
NM_001005862.2:c.2471A>C , LRG_724t1:c.2471A>C	NP_001005862.1:p.Lys824Thr
NM_001289936.1:c.2516A>C , LRG_724t4:c.2516A>C	NP_001276865.1:p.Lys839Thr
NM_001289937.1:c.2561A>C	NP_001276866.1:p.Lys854Thr
NM_004448.3:c.2561A>C , LRG_724t2:c.2561A>C	NP_004439.2:p.Lys854Thr
NR_110535.1:n.2885A>C
XM_024450641.1:c.2699A>C	XP_024306409.1:p.Lys900Thr
XM_024450642.1:c.2654A>C	XP_024306410.1:p.Lys885Thr
XM_024450643.1:c.2609A>C	XP_024306411.1:p.Lys870Thr
NM_001005862.3:c.2471A>C	NP_001005862.1:p.Lys824Thr
NM_001289936.2:c.2516A>C	NP_001276865.1:p.Lys839Thr
NM_001289937.2:c.2561A>C	NP_001276866.1:p.Lys854Thr
NM_001382782.1:c.2471A>C	NP_001369711.1:p.Lys824Thr
NM_001382783.1:c.2471A>C	NP_001369712.1:p.Lys824Thr
NM_001382784.1:c.2678A>C	NP_001369713.1:p.Lys893Thr
NM_001382785.1:c.2663A>C	NP_001369714.1:p.Lys888Thr
NM_001382786.1:c.2642A>C	NP_001369715.1:p.Lys881Thr
NM_001382787.1:c.2636A>C	NP_001369716.1:p.Lys879Thr
NM_001382788.1:c.2591A>C	NP_001369717.1:p.Lys864Thr
NM_001382789.1:c.2582A>C	NP_001369718.1:p.Lys861Thr
NM_001382790.1:c.2558A>C	NP_001369719.1:p.Lys853Thr
NM_001382791.1:c.2552A>C	NP_001369720.1:p.Lys851Thr
NM_001382792.1:c.2525A>C	NP_001369721.1:p.Lys842Thr
NM_001382793.1:c.2519A>C	NP_001369722.1:p.Lys840Thr
NM_001382794.1:c.2519A>C	NP_001369723.1:p.Lys840Thr
NM_001382795.1:c.2513A>C	NP_001369724.1:p.Lys838Thr
NM_001382796.1:c.2561A>C	NP_001369725.1:p.Lys854Thr
NM_001382797.1:c.2462A>C	NP_001369726.1:p.Lys821Thr
NM_001382798.1:c.2493+205A>C	NP_001369727.1:n.2493+205A>C
NM_001382799.1:c.2381A>C	NP_001369728.1:p.Lys794Thr
NM_001382800.1:c.2375A>C	NP_001369729.1:p.Lys792Thr
NM_001382801.1:c.2445+205A>C	NP_001369730.1:n.2445+205A>C
NM_001382802.1:c.2303A>C	NP_001369731.1:p.Lys768Thr
NM_001382803.1:c.2519A>C	NP_001369732.1:p.Lys840Thr
NM_001382804.1:c.1733A>C	NP_001369733.1:p.Lys578Thr
NM_001382805.1:c.2208+1456A>C	NP_001369734.1:n.2208+1456A>C
NM_001382806.1:c.1523A>C	NP_001369735.1:p.Lys508Thr
NM_004448.4:c.2561A>C MANE Select	NP_004439.2:p.Lys854Thr
NR_110535.2:n.2799A>C