Canonical Allele Identifier: CA1148845571
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013882A= , CM000663.2:g.1013882A= GRCh38
NC_000001.10:g.949262A= , CM000663.1:g.949262A= GRCh37
NC_000001.9:g.939125A= NCBI36
NG_033033.1:g.5416A=
NG_033033.2:g.17745A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-102A= ENSP00000485643.1:n.-21-102A=
ENST00000649529.1:c.4-102A= MANE Select ENSP00000496832.1:n.4-102A=
ENST00000379389.4:c.4-102A= ENSP00000368699.4:n.4-102A=
ENST00000624652.1:c.-21-102A= ENSP00000485313.1:n.-21-102A=
ENST00000624697.3:c.-21-102A= ENSP00000485643.1:n.-21-102A=
NM_005101.3:c.4-102A= NP_005092.1:n.4-102A=
NM_005101.4:c.4-102A= MANE Select NP_005092.1:n.4-102A=