Canonical Allele Identifier: CA337803876

Gene: ISG15

Linked Data

• MyVariant Identifiers: chr1:g.949489G>T (hg19) ; chr1:g.1014109G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014109G>T , CM000663.2:g.1014109G>T	GRCh38
NC_000001.10:g.949489G>T , CM000663.1:g.949489G>T	GRCh37
NC_000001.9:g.939352G>T	NCBI36
NG_033033.1:g.5643G>T
NG_033033.2:g.17972G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.105G>T	ENSP00000485643.1:p.Gln35His
ENST00000649529.1:c.129G>T MANE Select	ENSP00000496832.1:p.Gln43His
ENST00000379389.4:c.129G>T	ENSP00000368699.4:p.Gln43His
ENST00000624652.1:c.105G>T	ENSP00000485313.1:p.Gln35His
ENST00000624697.3:c.105G>T	ENSP00000485643.1:p.Gln35His
NM_005101.3:c.129G>T	NP_005092.1:p.Gln43His
NM_005101.4:c.129G>T MANE Select	NP_005092.1:p.Gln43His