Canonical Allele Identifier: CA2642487131
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1013848-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013848C>T , CM000663.2:g.1013848C>T GRCh38
NC_000001.10:g.949228C>T , CM000663.1:g.949228C>T GRCh37
NC_000001.9:g.939091C>T NCBI36
NG_033033.1:g.5382C>T
NG_033033.2:g.17711C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-136C>T ENSP00000485643.1:n.-21-136C>T
ENST00000649529.1:c.4-136C>T MANE Select ENSP00000496832.1:n.4-136C>T
ENST00000379389.4:c.4-136C>T ENSP00000368699.4:n.4-136C>T
ENST00000624652.1:c.-21-136C>T ENSP00000485313.1:n.-21-136C>T
ENST00000624697.3:c.-21-136C>T ENSP00000485643.1:n.-21-136C>T
NM_005101.3:c.4-136C>T NP_005092.1:n.4-136C>T
NM_005101.4:c.4-136C>T MANE Select NP_005092.1:n.4-136C>T