Canonical Allele Identifier: CA2642487249
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013868_1013869del , CM000663.2:g.1013868_1013869del GRCh38
NC_000001.10:g.949248_949249del , CM000663.1:g.949248_949249del GRCh37
NC_000001.9:g.939111_939112del NCBI36
NG_033033.1:g.5402_5403del
NG_033033.2:g.17731_17732del

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-116_-21-115del ENSP00000485643.1:n.-21-116_-21-115del
ENST00000649529.1:c.4-116_4-115del MANE Select ENSP00000496832.1:n.4-116_4-115del
ENST00000379389.4:c.4-116_4-115del ENSP00000368699.4:n.4-116_4-115del
ENST00000624652.1:c.-21-116_-21-115del ENSP00000485313.1:n.-21-116_-21-115del
ENST00000624697.3:c.-21-116_-21-115del ENSP00000485643.1:n.-21-116_-21-115del
NM_005101.3:c.4-116_4-115del NP_005092.1:n.4-116_4-115del
NM_005101.4:c.4-116_4-115del MANE Select NP_005092.1:n.4-116_4-115del