Canonical Allele Identifier: CA2642487372

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013927-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013927G>T , CM000663.2:g.1013927G>T	GRCh38
NC_000001.10:g.949307G>T , CM000663.1:g.949307G>T	GRCh37
NC_000001.9:g.939170G>T	NCBI36
NG_033033.1:g.5461G>T
NG_033033.2:g.17790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-57G>T	ENSP00000485643.1:n.-21-57G>T
ENST00000649529.1:c.4-57G>T MANE Select	ENSP00000496832.1:n.4-57G>T
ENST00000379389.4:c.4-57G>T	ENSP00000368699.4:n.4-57G>T
ENST00000624652.1:c.-21-57G>T	ENSP00000485313.1:n.-21-57G>T
ENST00000624697.3:c.-21-57G>T	ENSP00000485643.1:n.-21-57G>T
NM_005101.3:c.4-57G>T	NP_005092.1:n.4-57G>T
NM_005101.4:c.4-57G>T MANE Select	NP_005092.1:n.4-57G>T