Canonical Allele Identifier: CA2259228143
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725125A= , CM000679.2:g.39725125A= GRCh38
NC_000017.10:g.37881378A= , CM000679.1:g.37881378A= GRCh37
NC_000017.9:g.35134904A= NCBI36
NG_007503.1:g.41986A= , LRG_724:g.41986A=

Transcript Alleles

HGVS Amino-acid change
ENST00000269571.10:c.2570A= MANE Select ENSP00000269571.4:p.Asn857=
ENST00000269571.9:c.2570A= ENSP00000269571.4:p.Asn857=
ENST00000406381.6:c.2480A= ENSP00000385185.2:p.Asn827=
ENST00000445658.6:c.1742A= ENSP00000404047.2:p.Asn581=
ENST00000541774.5:c.2525A= ENSP00000446466.1:p.Asn842=
ENST00000578373.5:c.*2360A= ENSP00000463427.1:n.*2360A=
ENST00000580074.1:c.676A=
ENST00000583038.5:n.3704A=
ENST00000584450.5:c.2570A= ENSP00000463714.1:p.Asn857=
ENST00000584601.5:c.2480A= ENSP00000462438.1:p.Asn827=
NM_001005862.2:c.2480A= , LRG_724t1:c.2480A= NP_001005862.1:p.Asn827=
NM_001289936.1:c.2525A= , LRG_724t4:c.2525A= NP_001276865.1:p.Asn842=
NM_001289937.1:c.2570A= NP_001276866.1:p.Asn857=
NM_004448.3:c.2570A= , LRG_724t2:c.2570A= NP_004439.2:p.Asn857=
NR_110535.1:n.2894A=
XM_024450641.1:c.2708A= XP_024306409.1:p.Asn903=
XM_024450642.1:c.2663A= XP_024306410.1:p.Asn888=
XM_024450643.1:c.2618A= XP_024306411.1:p.Asn873=
NM_001005862.3:c.2480A= NP_001005862.1:p.Asn827=
NM_001289936.2:c.2525A= NP_001276865.1:p.Asn842=
NM_001289937.2:c.2570A= NP_001276866.1:p.Asn857=
NM_001382782.1:c.2480A= NP_001369711.1:p.Asn827=
NM_001382783.1:c.2480A= NP_001369712.1:p.Asn827=
NM_001382784.1:c.2687A= NP_001369713.1:p.Asn896=
NM_001382785.1:c.2672A= NP_001369714.1:p.Asn891=
NM_001382786.1:c.2651A= NP_001369715.1:p.Asn884=
NM_001382787.1:c.2645A= NP_001369716.1:p.Asn882=
NM_001382788.1:c.2600A= NP_001369717.1:p.Asn867=
NM_001382789.1:c.2591A= NP_001369718.1:p.Asn864=
NM_001382790.1:c.2567A= NP_001369719.1:p.Asn856=
NM_001382791.1:c.2561A= NP_001369720.1:p.Asn854=
NM_001382792.1:c.2534A= NP_001369721.1:p.Asn845=
NM_001382793.1:c.2528A= NP_001369722.1:p.Asn843=
NM_001382794.1:c.2528A= NP_001369723.1:p.Asn843=
NM_001382795.1:c.2522A= NP_001369724.1:p.Asn841=
NM_001382796.1:c.2570A= NP_001369725.1:p.Asn857=
NM_001382797.1:c.2471A= NP_001369726.1:p.Asn824=
NM_001382798.1:c.2494-202A= NP_001369727.1:n.2494-202A=
NM_001382799.1:c.2390A= NP_001369728.1:p.Asn797=
NM_001382800.1:c.2384A= NP_001369729.1:p.Asn795=
NM_001382801.1:c.2446-202A= NP_001369730.1:n.2446-202A=
NM_001382802.1:c.2312A= NP_001369731.1:p.Asn771=
NM_001382803.1:c.2528A= NP_001369732.1:p.Asn843=
NM_001382804.1:c.1742A= NP_001369733.1:p.Asn581=
NM_001382805.1:c.2208+1465A= NP_001369734.1:n.2208+1465A=
NM_001382806.1:c.1532A= NP_001369735.1:p.Asn511=
NM_004448.4:c.2570A= MANE Select NP_004439.2:p.Asn857=
NR_110535.2:n.2808A=