Canonical Allele Identifier: CA2642487312

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013884-C-CTCCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013884_1013885insTCCTGT , CM000663.2:g.1013884_1013885insTCCTGT	GRCh38
NC_000001.10:g.949264_949265insTCCTGT , CM000663.1:g.949264_949265insTCCTGT	GRCh37
NC_000001.9:g.939127_939128insTCCTGT	NCBI36
NG_033033.1:g.5418_5419insTCCTGT
NG_033033.2:g.17747_17748insTCCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-100_-21-99insTCCTGT	ENSP00000485643.1:n.-21-100_-21-99insTCCTGT
ENST00000649529.1:c.4-100_4-99insTCCTGT MANE Select	ENSP00000496832.1:n.4-100_4-99insTCCTGT
ENST00000379389.4:c.4-100_4-99insTCCTGT	ENSP00000368699.4:n.4-100_4-99insTCCTGT
ENST00000624652.1:c.-21-100_-21-99insTCCTGT	ENSP00000485313.1:n.-21-100_-21-99insTCCTGT
ENST00000624697.3:c.-21-100_-21-99insTCCTGT	ENSP00000485643.1:n.-21-100_-21-99insTCCTGT
NM_005101.3:c.4-100_4-99insTCCTGT	NP_005092.1:n.4-100_4-99insTCCTGT
NM_005101.4:c.4-100_4-99insTCCTGT MANE Select	NP_005092.1:n.4-100_4-99insTCCTGT