Canonical Allele Identifier: CA2642487291

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013877-G-GTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013877_1013878insTGT , CM000663.2:g.1013877_1013878insTGT	GRCh38
NC_000001.10:g.949257_949258insTGT , CM000663.1:g.949257_949258insTGT	GRCh37
NC_000001.9:g.939120_939121insTGT	NCBI36
NG_033033.1:g.5411_5412insTGT
NG_033033.2:g.17740_17741insTGT

Transcript Alleles

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