Canonical Allele Identifier: CA2642487179
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1013858-G-GT

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013858_1013859insT , CM000663.2:g.1013858_1013859insT GRCh38
NC_000001.10:g.949238_949239insT , CM000663.1:g.949238_949239insT GRCh37
NC_000001.9:g.939101_939102insT NCBI36
NG_033033.1:g.5392_5393insT
NG_033033.2:g.17721_17722insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-126_-21-125insT ENSP00000485643.1:n.-21-126_-21-125insT
ENST00000649529.1:c.4-126_4-125insT MANE Select ENSP00000496832.1:n.4-126_4-125insT
ENST00000379389.4:c.4-126_4-125insT ENSP00000368699.4:n.4-126_4-125insT
ENST00000624652.1:c.-21-126_-21-125insT ENSP00000485313.1:n.-21-126_-21-125insT
ENST00000624697.3:c.-21-126_-21-125insT ENSP00000485643.1:n.-21-126_-21-125insT
NM_005101.3:c.4-126_4-125insT NP_005092.1:n.4-126_4-125insT
NM_005101.4:c.4-126_4-125insT MANE Select NP_005092.1:n.4-126_4-125insT