Canonical Allele Identifier: CA2642487177

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013858-G-GGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013859_1013860insTTG , CM000663.2:g.1013859_1013860insTTG	GRCh38
NC_000001.10:g.949239_949240insTTG , CM000663.1:g.949239_949240insTTG	GRCh37
NC_000001.9:g.939102_939103insTTG	NCBI36
NG_033033.1:g.5393_5394insTTG
NG_033033.2:g.17722_17723insTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-125_-21-124insTTG	ENSP00000485643.1:n.-21-125_-21-124insTTG
ENST00000649529.1:c.4-125_4-124insTTG MANE Select	ENSP00000496832.1:n.4-125_4-124insTTG
ENST00000379389.4:c.4-125_4-124insTTG	ENSP00000368699.4:n.4-125_4-124insTTG
ENST00000624652.1:c.-21-125_-21-124insTTG	ENSP00000485313.1:n.-21-125_-21-124insTTG
ENST00000624697.3:c.-21-125_-21-124insTTG	ENSP00000485643.1:n.-21-125_-21-124insTTG
NM_005101.3:c.4-125_4-124insTTG	NP_005092.1:n.4-125_4-124insTTG
NM_005101.4:c.4-125_4-124insTTG MANE Select	NP_005092.1:n.4-125_4-124insTTG