Canonical Allele Identifier: CA2742133442
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013857_1013858insAGTTAT , CM000663.2:g.1013857_1013858insAGTTAT GRCh38
NC_000001.10:g.949237_949238insAGTTAT , CM000663.1:g.949237_949238insAGTTAT GRCh37
NC_000001.9:g.939100_939101insAGTTAT NCBI36
NG_033033.1:g.5391_5392insAGTTAT
NG_033033.2:g.17720_17721insAGTTAT

Transcript Alleles

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