Canonical Allele Identifier: CA2642487322

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013887-T-TCGGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013887_1013888insCGGTG , CM000663.2:g.1013887_1013888insCGGTG	GRCh38
NC_000001.10:g.949267_949268insCGGTG , CM000663.1:g.949267_949268insCGGTG	GRCh37
NC_000001.9:g.939130_939131insCGGTG	NCBI36
NG_033033.1:g.5421_5422insCGGTG
NG_033033.2:g.17750_17751insCGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-97_-21-96insCGGTG	ENSP00000485643.1:n.-21-97_-21-96insCGGTG
ENST00000649529.1:c.4-97_4-96insCGGTG MANE Select	ENSP00000496832.1:n.4-97_4-96insCGGTG
ENST00000379389.4:c.4-97_4-96insCGGTG	ENSP00000368699.4:n.4-97_4-96insCGGTG
ENST00000624652.1:c.-21-97_-21-96insCGGTG	ENSP00000485313.1:n.-21-97_-21-96insCGGTG
ENST00000624697.3:c.-21-97_-21-96insCGGTG	ENSP00000485643.1:n.-21-97_-21-96insCGGTG
NM_005101.3:c.4-97_4-96insCGGTG	NP_005092.1:n.4-97_4-96insCGGTG
NM_005101.4:c.4-97_4-96insCGGTG MANE Select	NP_005092.1:n.4-97_4-96insCGGTG