Canonical Allele Identifier: CA2642487303
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013882_1013883del , CM000663.2:g.1013882_1013883del GRCh38
NC_000001.10:g.949262_949263del , CM000663.1:g.949262_949263del GRCh37
NC_000001.9:g.939125_939126del NCBI36
NG_033033.1:g.5416_5417del
NG_033033.2:g.17745_17746del

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-102_-21-101del ENSP00000485643.1:n.-21-102_-21-101del
ENST00000649529.1:c.4-102_4-101del MANE Select ENSP00000496832.1:n.4-102_4-101del
ENST00000379389.4:c.4-102_4-101del ENSP00000368699.4:n.4-102_4-101del
ENST00000624652.1:c.-21-102_-21-101del ENSP00000485313.1:n.-21-102_-21-101del
ENST00000624697.3:c.-21-102_-21-101del ENSP00000485643.1:n.-21-102_-21-101del
NM_005101.3:c.4-102_4-101del NP_005092.1:n.4-102_4-101del
NM_005101.4:c.4-102_4-101del MANE Select NP_005092.1:n.4-102_4-101del