Canonical Allele Identifier: CA2642487282
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1013875-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013875A>T , CM000663.2:g.1013875A>T GRCh38
NC_000001.10:g.949255A>T , CM000663.1:g.949255A>T GRCh37
NC_000001.9:g.939118A>T NCBI36
NG_033033.1:g.5409A>T
NG_033033.2:g.17738A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-109A>T ENSP00000485643.1:n.-21-109A>T
ENST00000649529.1:c.4-109A>T MANE Select ENSP00000496832.1:n.4-109A>T
ENST00000379389.4:c.4-109A>T ENSP00000368699.4:n.4-109A>T
ENST00000624652.1:c.-21-109A>T ENSP00000485313.1:n.-21-109A>T
ENST00000624697.3:c.-21-109A>T ENSP00000485643.1:n.-21-109A>T
NM_005101.3:c.4-109A>T NP_005092.1:n.4-109A>T
NM_005101.4:c.4-109A>T MANE Select NP_005092.1:n.4-109A>T