Canonical Allele Identifier: CA337803512

Gene: ISG15

Linked Data

• MyVariant Identifiers: chr1:g.949405C>A (hg19) ; chr1:g.1014025C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014025C>A , CM000663.2:g.1014025C>A	GRCh38
NC_000001.10:g.949405C>A , CM000663.1:g.949405C>A	GRCh37
NC_000001.9:g.939268C>A	NCBI36
NG_033033.1:g.5559C>A
NG_033033.2:g.17888C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.21C>A	ENSP00000485643.1:p.Phe7Leu
ENST00000649529.1:c.45C>A MANE Select	ENSP00000496832.1:p.Phe15Leu
ENST00000379389.4:c.45C>A	ENSP00000368699.4:p.Phe15Leu
ENST00000624652.1:c.21C>A	ENSP00000485313.1:p.Phe7Leu
ENST00000624697.3:c.21C>A	ENSP00000485643.1:p.Phe7Leu
NM_005101.3:c.45C>A	NP_005092.1:p.Phe15Leu
NM_005101.4:c.45C>A MANE Select	NP_005092.1:p.Phe15Leu