Canonical Allele Identifier: CA2642487288
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1013878-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013878A>G , CM000663.2:g.1013878A>G GRCh38
NC_000001.10:g.949258A>G , CM000663.1:g.949258A>G GRCh37
NC_000001.9:g.939121A>G NCBI36
NG_033033.1:g.5412A>G
NG_033033.2:g.17741A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-106A>G ENSP00000485643.1:n.-21-106A>G
ENST00000649529.1:c.4-106A>G MANE Select ENSP00000496832.1:n.4-106A>G
ENST00000379389.4:c.4-106A>G ENSP00000368699.4:n.4-106A>G
ENST00000624652.1:c.-21-106A>G ENSP00000485313.1:n.-21-106A>G
ENST00000624697.3:c.-21-106A>G ENSP00000485643.1:n.-21-106A>G
NM_005101.3:c.4-106A>G NP_005092.1:n.4-106A>G
NM_005101.4:c.4-106A>G MANE Select NP_005092.1:n.4-106A>G