Canonical Allele Identifier: CA337804449

Gene: ISG15

Linked Data

• gnomAD v4: 1-1014204-T-G
• MyVariant Identifiers: chr1:g.949584T>G (hg19) ; chr1:g.1014204T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014204T>G , CM000663.2:g.1014204T>G	GRCh38
NC_000001.10:g.949584T>G , CM000663.1:g.949584T>G	GRCh37
NC_000001.9:g.939447T>G	NCBI36
NG_033033.1:g.5738T>G
NG_033033.2:g.18067T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.200T>G	ENSP00000485643.1:p.Val67Gly
ENST00000649529.1:c.224T>G MANE Select	ENSP00000496832.1:p.Val75Gly
ENST00000379389.4:c.224T>G	ENSP00000368699.4:p.Val75Gly
ENST00000624652.1:c.200T>G	ENSP00000485313.1:p.Val67Gly
ENST00000624697.3:c.200T>G	ENSP00000485643.1:p.Val67Gly
NM_005101.3:c.224T>G	NP_005092.1:p.Val75Gly
NM_005101.4:c.224T>G MANE Select	NP_005092.1:p.Val75Gly