Canonical Allele Identifier: CA415757008

Gene: ISG15

Linked Data

• gnomAD v4: 1-1014247-C-T
• MyVariant Identifiers: chr1:g.949627C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014247C>T , CM000663.2:g.1014247C>T	GRCh38
NC_000001.10:g.949627C>T , CM000663.1:g.949627C>T	GRCh37
NC_000001.9:g.939490C>T	NCBI36
NG_033033.1:g.5781C>T
NG_033033.2:g.18110C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.243C>T	ENSP00000485643.1:p.Asn81=
ENST00000649529.1:c.267C>T MANE Select	ENSP00000496832.1:p.Asn89=
ENST00000379389.4:c.267C>T	ENSP00000368699.4:p.Asn89=
ENST00000624652.1:c.243C>T	ENSP00000485313.1:p.Asn81=
ENST00000624697.3:c.243C>T	ENSP00000485643.1:p.Asn81=
NM_005101.3:c.267C>T	NP_005092.1:p.Asn89=
NM_005101.4:c.267C>T MANE Select	NP_005092.1:p.Asn89=