Canonical Allele Identifier: CA2642487292

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013877-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013877_1013878insT , CM000663.2:g.1013877_1013878insT	GRCh38
NC_000001.10:g.949257_949258insT , CM000663.1:g.949257_949258insT	GRCh37
NC_000001.9:g.939120_939121insT	NCBI36
NG_033033.1:g.5411_5412insT
NG_033033.2:g.17740_17741insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-107_-21-106insT	ENSP00000485643.1:n.-21-107_-21-106insT
ENST00000649529.1:c.4-107_4-106insT MANE Select	ENSP00000496832.1:n.4-107_4-106insT
ENST00000379389.4:c.4-107_4-106insT	ENSP00000368699.4:n.4-107_4-106insT
ENST00000624652.1:c.-21-107_-21-106insT	ENSP00000485313.1:n.-21-107_-21-106insT
ENST00000624697.3:c.-21-107_-21-106insT	ENSP00000485643.1:n.-21-107_-21-106insT
NM_005101.3:c.4-107_4-106insT	NP_005092.1:n.4-107_4-106insT
NM_005101.4:c.4-107_4-106insT MANE Select	NP_005092.1:n.4-107_4-106insT