Canonical Allele Identifier: CA337803712

Gene: ISG15

Linked Data

• MyVariant Identifiers: chr1:g.949458C>G (hg19) ; chr1:g.1014078C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014078C>G , CM000663.2:g.1014078C>G	GRCh38
NC_000001.10:g.949458C>G , CM000663.1:g.949458C>G	GRCh37
NC_000001.9:g.939321C>G	NCBI36
NG_033033.1:g.5612C>G
NG_033033.2:g.17941C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.74C>G	ENSP00000485643.1:p.Thr25Ser
ENST00000649529.1:c.98C>G MANE Select	ENSP00000496832.1:p.Thr33Ser
ENST00000379389.4:c.98C>G	ENSP00000368699.4:p.Thr33Ser
ENST00000624652.1:c.74C>G	ENSP00000485313.1:p.Thr25Ser
ENST00000624697.3:c.74C>G	ENSP00000485643.1:p.Thr25Ser
NM_005101.3:c.98C>G	NP_005092.1:p.Thr33Ser
NM_005101.4:c.98C>G MANE Select	NP_005092.1:p.Thr33Ser