Canonical Allele Identifier: CA2187544911
Community Standard Title: NM_020851.3(ISLR2):c.-8-540A=
Gene: ISLR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74132207A= , CM000677.2:g.74132207A= GRCh38
NC_000015.9:g.74424548A= , CM000677.1:g.74424548A= GRCh37
NC_000015.8:g.72211601A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_020851.3:c.-8-540A= MANE Select NP_065902.1:n.-8-540A=
ENST00000453268.3:c.-8-540A= MANE Select ENSP00000411834.2:n.-8-540A=
NM_001130136.1:c.-8-540A= NP_001123608.1:n.-8-540A=
NM_001130137.1:c.-8-540A= NP_001123609.1:n.-8-540A=
NM_001130138.1:c.-8-540A= NP_001123610.1:n.-8-540A=
NM_001130138.2:c.-8-540A= NP_001123610.1:n.-8-540A=
NM_020851.2:c.-8-540A= NP_065902.1:n.-8-540A=
ENST00000361742.7:c.-8-540A= ENSP00000355402.3:n.-8-540A=
ENST00000419208.2:c.-8-540A= ENSP00000408872.2:n.-8-540A=
ENST00000435464.5:c.-8-540A= ENSP00000411443.1:n.-8-540A=
ENST00000453268.2:c.-8-540A= ENSP00000411834.2:n.-8-540A=
ENST00000561740.5:c.-8-540A= ENSP00000455076.1:n.-8-540A=
ENST00000561975.5:n.338+891A=
ENST00000565159.5:c.-8-540A= ENSP00000455531.1:n.-8-540A=
ENST00000565332.1:c.-8-540A= ENSP00000454259.1:n.-8-540A=
ENST00000565540.1:c.-9+198A= ENSP00000458080.1:n.-9+198A=
ENST00000567206.5:c.-8-540A= ENSP00000454859.1:n.-8-540A=
ENST00000569886.5:c.-8-540A= ENSP00000454287.1:n.-8-540A=
XM_011521840.1:c.-8-540A= XP_011520142.1:n.-8-540A=
XM_011521840.3:c.-8-540A= XP_011520142.1:n.-8-540A=
XM_011521841.1:c.-8-540A= XP_011520143.1:n.-8-540A=
XM_011521842.1:c.-8-540A= XP_011520144.1:n.-8-540A=
XM_017022446.2:c.-8-540A= XP_016877935.1:n.-8-540A=
XM_024450003.1:c.-8-540A= XP_024305771.1:n.-8-540A=
XM_024450004.1:c.-8-540A= XP_024305772.1:n.-8-540A=
XM_024450005.1:c.-8-540A= XP_024305773.1:n.-8-540A=
XM_024450006.1:c.-8-540A= XP_024305774.1:n.-8-540A=
XM_024450007.1:c.-8-540A= XP_024305775.1:n.-8-540A=
XM_024450008.1:c.-8-540A= XP_024305776.1:n.-8-540A=
XR_931875.1:n.111-540A=
XR_931875.3:n.331-540A=