Canonical Allele Identifier: CA337803697

Gene: ISG15

Linked Data

• gnomAD v4: 1-1014074-A-T
• MyVariant Identifiers: chr1:g.949454A>T (hg19) ; chr1:g.1014074A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014074A>T , CM000663.2:g.1014074A>T	GRCh38
NC_000001.10:g.949454A>T , CM000663.1:g.949454A>T	GRCh37
NC_000001.9:g.939317A>T	NCBI36
NG_033033.1:g.5608A>T
NG_033033.2:g.17937A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.70A>T	ENSP00000485643.1:p.Ile24Phe
ENST00000649529.1:c.94A>T MANE Select	ENSP00000496832.1:p.Ile32Phe
ENST00000379389.4:c.94A>T	ENSP00000368699.4:p.Ile32Phe
ENST00000624652.1:c.70A>T	ENSP00000485313.1:p.Ile24Phe
ENST00000624697.3:c.70A>T	ENSP00000485643.1:p.Ile24Phe
NM_005101.3:c.94A>T	NP_005092.1:p.Ile32Phe
NM_005101.4:c.94A>T MANE Select	NP_005092.1:p.Ile32Phe