Canonical Allele Identifier: CA1148734732

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014223_1014232delinsTCTGAGCATC , CM000663.2:g.1014223_1014232delinsTCTGAGCATC	GRCh38
NC_000001.10:g.949603_949612delinsTCTGAGCATC , CM000663.1:g.949603_949612delinsTCTGAGCATC	GRCh37
NC_000001.9:g.939466_939475delinsTCTGAGCATC	NCBI36
NG_033033.1:g.5757_5766delinsTCTGAGCATC
NG_033033.2:g.18086_18095delinsTCTGAGCATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000624697.4:c.219_228delinsTCTGAGCATC	ENSP00000485643.1:p.Pro73=
ENST00000649529.1:c.243_252delinsTCTGAGCATC MANE Select	ENSP00000496832.1:p.Pro81=
ENST00000379389.4:c.243_252delinsTCTGAGCATC	ENSP00000368699.4:p.Pro81=
ENST00000624652.1:c.219_228delinsTCTGAGCATC	ENSP00000485313.1:p.Pro73=
ENST00000624697.3:c.219_228delinsTCTGAGCATC	ENSP00000485643.1:p.Pro73=
NM_005101.3:c.243_252delinsTCTGAGCATC	NP_005092.1:p.Pro81=
NM_005101.4:c.243_252delinsTCTGAGCATC MANE Select	NP_005092.1:p.Pro81=