Canonical Allele Identifier: CA2642487233

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013863-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013863_1013864insC , CM000663.2:g.1013863_1013864insC	GRCh38
NC_000001.10:g.949243_949244insC , CM000663.1:g.949243_949244insC	GRCh37
NC_000001.9:g.939106_939107insC	NCBI36
NG_033033.1:g.5397_5398insC
NG_033033.2:g.17726_17727insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-121_-21-120insC	ENSP00000485643.1:n.-21-121_-21-120insC
ENST00000649529.1:c.4-121_4-120insC MANE Select	ENSP00000496832.1:n.4-121_4-120insC
ENST00000379389.4:c.4-121_4-120insC	ENSP00000368699.4:n.4-121_4-120insC
ENST00000624652.1:c.-21-121_-21-120insC	ENSP00000485313.1:n.-21-121_-21-120insC
ENST00000624697.3:c.-21-121_-21-120insC	ENSP00000485643.1:n.-21-121_-21-120insC
NM_005101.3:c.4-121_4-120insC	NP_005092.1:n.4-121_4-120insC
NM_005101.4:c.4-121_4-120insC MANE Select	NP_005092.1:n.4-121_4-120insC