Canonical Allele Identifier: CA2642487308

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013883-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013883_1013884insGT , CM000663.2:g.1013883_1013884insGT	GRCh38
NC_000001.10:g.949263_949264insGT , CM000663.1:g.949263_949264insGT	GRCh37
NC_000001.9:g.939126_939127insGT	NCBI36
NG_033033.1:g.5417_5418insGT
NG_033033.2:g.17746_17747insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-101_-21-100insGT	ENSP00000485643.1:n.-21-101_-21-100insGT
ENST00000649529.1:c.4-101_4-100insGT MANE Select	ENSP00000496832.1:n.4-101_4-100insGT
ENST00000379389.4:c.4-101_4-100insGT	ENSP00000368699.4:n.4-101_4-100insGT
ENST00000624652.1:c.-21-101_-21-100insGT	ENSP00000485313.1:n.-21-101_-21-100insGT
ENST00000624697.3:c.-21-101_-21-100insGT	ENSP00000485643.1:n.-21-101_-21-100insGT
NM_005101.3:c.4-101_4-100insGT	NP_005092.1:n.4-101_4-100insGT
NM_005101.4:c.4-101_4-100insGT MANE Select	NP_005092.1:n.4-101_4-100insGT