Canonical Allele Identifier: CA337803411

Gene: ISG15

Linked Data

• MyVariant Identifiers: chr1:g.949379G>C (hg19) ; chr1:g.1013999G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013999G>C , CM000663.2:g.1013999G>C	GRCh38
NC_000001.10:g.949379G>C , CM000663.1:g.949379G>C	GRCh37
NC_000001.9:g.939242G>C	NCBI36
NG_033033.1:g.5533G>C
NG_033033.2:g.17862G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-6G>C	ENSP00000485643.1:n.-6G>C
ENST00000649529.1:c.19G>C MANE Select	ENSP00000496832.1:p.Val7Leu
ENST00000379389.4:c.19G>C	ENSP00000368699.4:p.Val7Leu
ENST00000624652.1:c.-6G>C	ENSP00000485313.1:n.-6G>C
ENST00000624697.3:c.-6G>C	ENSP00000485643.1:n.-6G>C
NM_005101.3:c.19G>C	NP_005092.1:p.Val7Leu
NM_005101.4:c.19G>C MANE Select	NP_005092.1:p.Val7Leu