Canonical Allele Identifier: CA2642487268

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013872-G-GTGCTCCCTCCTGTCTGTCCTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013872_1013873insTGCTCCCTCCTGTCTGTCCTCT , CM000663.2:g.1013872_1013873insTGCTCCCTCCTGTCTGTCCTCT	GRCh38
NC_000001.10:g.949252_949253insTGCTCCCTCCTGTCTGTCCTCT , CM000663.1:g.949252_949253insTGCTCCCTCCTGTCTGTCCTCT	GRCh37
NC_000001.9:g.939115_939116insTGCTCCCTCCTGTCTGTCCTCT	NCBI36
NG_033033.1:g.5406_5407insTGCTCCCTCCTGTCTGTCCTCT
NG_033033.2:g.17735_17736insTGCTCCCTCCTGTCTGTCCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-112_-21-111insTGCTCCCTCCTGTCTGTCCTCT	ENSP00000485643.1:n.-21-112_-21-111insTGCTCCCTCCTGTCTGTCCTCT
ENST00000649529.1:c.4-112_4-111insTGCTCCCTCCTGTCTGTCCTCT MANE Select	ENSP00000496832.1:n.4-112_4-111insTGCTCCCTCCTGTCTGTCCTCT
ENST00000379389.4:c.4-112_4-111insTGCTCCCTCCTGTCTGTCCTCT	ENSP00000368699.4:n.4-112_4-111insTGCTCCCTCCTGTCTGTCCTCT
ENST00000624652.1:c.-21-112_-21-111insTGCTCCCTCCTGTCTGTCCTCT	ENSP00000485313.1:n.-21-112_-21-111insTGCTCCCTCCTGTCTGTCCTCT
ENST00000624697.3:c.-21-112_-21-111insTGCTCCCTCCTGTCTGTCCTCT	ENSP00000485643.1:n.-21-112_-21-111insTGCTCCCTCCTGTCTGTCCTCT
NM_005101.3:c.4-112_4-111insTGCTCCCTCCTGTCTGTCCTCT	NP_005092.1:n.4-112_4-111insTGCTCCCTCCTGTCTGTCCTCT
NM_005101.4:c.4-112_4-111insTGCTCCCTCCTGTCTGTCCTCT MANE Select	NP_005092.1:n.4-112_4-111insTGCTCCCTCCTGTCTGTCCTCT