Canonical Allele Identifier: CA337804079
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949521T>C (hg19) chr1:g.1014141T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014141T>C , CM000663.2:g.1014141T>C GRCh38
NC_000001.10:g.949521T>C , CM000663.1:g.949521T>C GRCh37
NC_000001.9:g.939384T>C NCBI36
NG_033033.1:g.5675T>C
NG_033033.2:g.18004T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.137T>C ENSP00000485643.1:p.Leu46Pro
ENST00000649529.1:c.161T>C MANE Select ENSP00000496832.1:p.Leu54Pro
ENST00000379389.4:c.161T>C ENSP00000368699.4:p.Leu54Pro
ENST00000624652.1:c.137T>C ENSP00000485313.1:p.Leu46Pro
ENST00000624697.3:c.137T>C ENSP00000485643.1:p.Leu46Pro
NM_005101.3:c.161T>C NP_005092.1:p.Leu54Pro
NM_005101.4:c.161T>C MANE Select NP_005092.1:p.Leu54Pro
Search 100 bp 5'
Search 100 bp 3'