Canonical Allele Identifier: CA499890105

Gene: ERBB2

Linked Data

• MyVariant Identifiers: chr17:g.37881338A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725085A>C , CM000679.2:g.39725085A>C	GRCh38
NC_000017.10:g.37881338A>C , CM000679.1:g.37881338A>C	GRCh37
NC_000017.9:g.35134864A>C	NCBI36
NG_007503.1:g.41946A>C , LRG_724:g.41946A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2530A>C MANE Select	ENSP00000269571.4:p.Arg844=
ENST00000269571.9:c.2530A>C	ENSP00000269571.4:p.Arg844=
ENST00000406381.6:c.2440A>C	ENSP00000385185.2:p.Arg814=
ENST00000445658.6:c.1702A>C	ENSP00000404047.2:p.Arg568=
ENST00000541774.5:c.2485A>C	ENSP00000446466.1:p.Arg829=
ENST00000578373.5:c.*2320A>C	ENSP00000463427.1:n.*2320A>C
ENST00000580074.1:c.636A>C
ENST00000583038.5:n.3664A>C
ENST00000584450.5:c.2530A>C	ENSP00000463714.1:p.Arg844=
ENST00000584601.5:c.2440A>C	ENSP00000462438.1:p.Arg814=
NM_001005862.2:c.2440A>C , LRG_724t1:c.2440A>C	NP_001005862.1:p.Arg814=
NM_001289936.1:c.2485A>C , LRG_724t4:c.2485A>C	NP_001276865.1:p.Arg829=
NM_001289937.1:c.2530A>C	NP_001276866.1:p.Arg844=
NM_004448.3:c.2530A>C , LRG_724t2:c.2530A>C	NP_004439.2:p.Arg844=
NR_110535.1:n.2854A>C
XM_024450641.1:c.2668A>C	XP_024306409.1:p.Arg890=
XM_024450642.1:c.2623A>C	XP_024306410.1:p.Arg875=
XM_024450643.1:c.2578A>C	XP_024306411.1:p.Arg860=
NM_001005862.3:c.2440A>C	NP_001005862.1:p.Arg814=
NM_001289936.2:c.2485A>C	NP_001276865.1:p.Arg829=
NM_001289937.2:c.2530A>C	NP_001276866.1:p.Arg844=
NM_001382782.1:c.2440A>C	NP_001369711.1:p.Arg814=
NM_001382783.1:c.2440A>C	NP_001369712.1:p.Arg814=
NM_001382784.1:c.2647A>C	NP_001369713.1:p.Arg883=
NM_001382785.1:c.2632A>C	NP_001369714.1:p.Arg878=
NM_001382786.1:c.2611A>C	NP_001369715.1:p.Arg871=
NM_001382787.1:c.2605A>C	NP_001369716.1:p.Arg869=
NM_001382788.1:c.2560A>C	NP_001369717.1:p.Arg854=
NM_001382789.1:c.2551A>C	NP_001369718.1:p.Arg851=
NM_001382790.1:c.2527A>C	NP_001369719.1:p.Arg843=
NM_001382791.1:c.2521A>C	NP_001369720.1:p.Arg841=
NM_001382792.1:c.2494A>C	NP_001369721.1:p.Arg832=
NM_001382793.1:c.2488A>C	NP_001369722.1:p.Arg830=
NM_001382794.1:c.2488A>C	NP_001369723.1:p.Arg830=
NM_001382795.1:c.2482A>C	NP_001369724.1:p.Arg828=
NM_001382796.1:c.2530A>C	NP_001369725.1:p.Arg844=
NM_001382797.1:c.2431A>C	NP_001369726.1:p.Arg811=
NM_001382798.1:c.2493+174A>C	NP_001369727.1:n.2493+174A>C
NM_001382799.1:c.2350A>C	NP_001369728.1:p.Arg784=
NM_001382800.1:c.2344A>C	NP_001369729.1:p.Arg782=
NM_001382801.1:c.2445+174A>C	NP_001369730.1:n.2445+174A>C
NM_001382802.1:c.2272A>C	NP_001369731.1:p.Arg758=
NM_001382803.1:c.2488A>C	NP_001369732.1:p.Arg830=
NM_001382804.1:c.1702A>C	NP_001369733.1:p.Arg568=
NM_001382805.1:c.2208+1425A>C	NP_001369734.1:n.2208+1425A>C
NM_001382806.1:c.1492A>C	NP_001369735.1:p.Arg498=
NM_004448.4:c.2530A>C MANE Select	NP_004439.2:p.Arg844=
NR_110535.2:n.2768A>C