Canonical Allele Identifier: CA2642487269
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013880_1013904del , CM000663.2:g.1013880_1013904del GRCh38
NC_000001.10:g.949260_949284del , CM000663.1:g.949260_949284del GRCh37
NC_000001.9:g.939123_939147del NCBI36
NG_033033.1:g.5414_5438del
NG_033033.2:g.17743_17767del

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-104_-21-80del ENSP00000485643.1:n.-21-104_-21-80del
ENST00000649529.1:c.4-104_4-80del MANE Select ENSP00000496832.1:n.4-104_4-80del
ENST00000379389.4:c.4-104_4-80del ENSP00000368699.4:n.4-104_4-80del
ENST00000624652.1:c.-21-104_-21-80del ENSP00000485313.1:n.-21-104_-21-80del
ENST00000624697.3:c.-21-104_-21-80del ENSP00000485643.1:n.-21-104_-21-80del
NM_005101.3:c.4-104_4-80del NP_005092.1:n.4-104_4-80del
NM_005101.4:c.4-104_4-80del MANE Select NP_005092.1:n.4-104_4-80del