Canonical Allele Identifier: CA507620

Gene: ISG15

Linked Data

• dbSNP Id: rs202075563
• ExAC: 1:949472 G / T
• gnomAD v2: 1-949472-G-T
• MyVariant Identifiers: chr1:g.949472G>T (hg19) ; chr1:g.1014092G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014092G>T , CM000663.2:g.1014092G>T	GRCh38
NC_000001.10:g.949472G>T , CM000663.1:g.949472G>T	GRCh37
NC_000001.9:g.939335G>T	NCBI36
NG_033033.1:g.5626G>T
NG_033033.2:g.17955G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.88G>T	ENSP00000485643.1:p.Val30Leu
ENST00000649529.1:c.112G>T MANE Select	ENSP00000496832.1:p.Val38Leu
ENST00000379389.4:c.112G>T	ENSP00000368699.4:p.Val38Leu
ENST00000624652.1:c.88G>T	ENSP00000485313.1:p.Val30Leu
ENST00000624697.3:c.88G>T	ENSP00000485643.1:p.Val30Leu
NM_005101.3:c.112G>T	NP_005092.1:p.Val38Leu
NM_005101.4:c.112G>T MANE Select	NP_005092.1:p.Val38Leu