Canonical Allele Identifier: CA507587

Gene: ISG15

Linked Data

• dbSNP Id: rs759380949
• ExAC: 1:949335 C / T
• gnomAD v2: 1-949335-C-T
• MyVariant Identifiers: chr1:g.949335C>T (hg19) ; chr1:g.1013955C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013955C>T , CM000663.2:g.1013955C>T	GRCh38
NC_000001.10:g.949335C>T , CM000663.1:g.949335C>T	GRCh37
NC_000001.9:g.939198C>T	NCBI36
NG_033033.1:g.5489C>T
NG_033033.2:g.17818C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-29C>T	ENSP00000485643.1:n.-21-29C>T
ENST00000649529.1:c.4-29C>T MANE Select	ENSP00000496832.1:n.4-29C>T
ENST00000379389.4:c.4-29C>T	ENSP00000368699.4:n.4-29C>T
ENST00000624652.1:c.-21-29C>T	ENSP00000485313.1:n.-21-29C>T
ENST00000624697.3:c.-21-29C>T	ENSP00000485643.1:n.-21-29C>T
NM_005101.3:c.4-29C>T	NP_005092.1:n.4-29C>T
NM_005101.4:c.4-29C>T MANE Select	NP_005092.1:n.4-29C>T