Canonical Allele Identifier: CA2642487162
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013857_1013858insAATGAAGT , CM000663.2:g.1013857_1013858insAATGAAGT GRCh38
NC_000001.10:g.949237_949238insAATGAAGT , CM000663.1:g.949237_949238insAATGAAGT GRCh37
NC_000001.9:g.939100_939101insAATGAAGT NCBI36
NG_033033.1:g.5391_5392insAATGAAGT
NG_033033.2:g.17720_17721insAATGAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-127_-21-126insAATGAAGT ENSP00000485643.1:n.-21-127_-21-126insAATGAAGT
ENST00000649529.1:c.4-127_4-126insAATGAAGT MANE Select ENSP00000496832.1:n.4-127_4-126insAATGAAGT
ENST00000379389.4:c.4-127_4-126insAATGAAGT ENSP00000368699.4:n.4-127_4-126insAATGAAGT
ENST00000624652.1:c.-21-127_-21-126insAATGAAGT ENSP00000485313.1:n.-21-127_-21-126insAATGAAGT
ENST00000624697.3:c.-21-127_-21-126insAATGAAGT ENSP00000485643.1:n.-21-127_-21-126insAATGAAGT
NM_005101.3:c.4-127_4-126insAATGAAGT NP_005092.1:n.4-127_4-126insAATGAAGT
NM_005101.4:c.4-127_4-126insAATGAAGT MANE Select NP_005092.1:n.4-127_4-126insAATGAAGT