Canonical Allele Identifier: CA2642487294
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013879_1013880insATCTG , CM000663.2:g.1013879_1013880insATCTG GRCh38
NC_000001.10:g.949259_949260insATCTG , CM000663.1:g.949259_949260insATCTG GRCh37
NC_000001.9:g.939122_939123insATCTG NCBI36
NG_033033.1:g.5413_5414insATCTG
NG_033033.2:g.17742_17743insATCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-105_-21-104insATCTG ENSP00000485643.1:n.-21-105_-21-104insATCTG
ENST00000649529.1:c.4-105_4-104insATCTG MANE Select ENSP00000496832.1:n.4-105_4-104insATCTG
ENST00000379389.4:c.4-105_4-104insATCTG ENSP00000368699.4:n.4-105_4-104insATCTG
ENST00000624652.1:c.-21-105_-21-104insATCTG ENSP00000485313.1:n.-21-105_-21-104insATCTG
ENST00000624697.3:c.-21-105_-21-104insATCTG ENSP00000485643.1:n.-21-105_-21-104insATCTG
NM_005101.3:c.4-105_4-104insATCTG NP_005092.1:n.4-105_4-104insATCTG
NM_005101.4:c.4-105_4-104insATCTG MANE Select NP_005092.1:n.4-105_4-104insATCTG