Canonical Allele Identifier: CA2642487293

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013878-A-ATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013878_1013879insTCT , CM000663.2:g.1013878_1013879insTCT	GRCh38
NC_000001.10:g.949258_949259insTCT , CM000663.1:g.949258_949259insTCT	GRCh37
NC_000001.9:g.939121_939122insTCT	NCBI36
NG_033033.1:g.5412_5413insTCT
NG_033033.2:g.17741_17742insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-106_-21-105insTCT	ENSP00000485643.1:n.-21-106_-21-105insTCT
ENST00000649529.1:c.4-106_4-105insTCT MANE Select	ENSP00000496832.1:n.4-106_4-105insTCT
ENST00000379389.4:c.4-106_4-105insTCT	ENSP00000368699.4:n.4-106_4-105insTCT
ENST00000624652.1:c.-21-106_-21-105insTCT	ENSP00000485313.1:n.-21-106_-21-105insTCT
ENST00000624697.3:c.-21-106_-21-105insTCT	ENSP00000485643.1:n.-21-106_-21-105insTCT
NM_005101.3:c.4-106_4-105insTCT	NP_005092.1:n.4-106_4-105insTCT
NM_005101.4:c.4-106_4-105insTCT MANE Select	NP_005092.1:n.4-106_4-105insTCT