Canonical Allele Identifier: CA2742133447

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013860_1013861insGTG , CM000663.2:g.1013860_1013861insGTG	GRCh38
NC_000001.10:g.949240_949241insGTG , CM000663.1:g.949240_949241insGTG	GRCh37
NC_000001.9:g.939103_939104insGTG	NCBI36
NG_033033.1:g.5394_5395insGTG
NG_033033.2:g.17723_17724insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-124_-21-123insGTG	ENSP00000485643.1:n.-21-124_-21-123insGTG
ENST00000649529.1:c.4-124_4-123insGTG MANE Select	ENSP00000496832.1:n.4-124_4-123insGTG
ENST00000379389.4:c.4-124_4-123insGTG	ENSP00000368699.4:n.4-124_4-123insGTG
ENST00000624652.1:c.-21-124_-21-123insGTG	ENSP00000485313.1:n.-21-124_-21-123insGTG
ENST00000624697.3:c.-21-124_-21-123insGTG	ENSP00000485643.1:n.-21-124_-21-123insGTG
NM_005101.3:c.4-124_4-123insGTG	NP_005092.1:n.4-124_4-123insGTG
NM_005101.4:c.4-124_4-123insGTG MANE Select	NP_005092.1:n.4-124_4-123insGTG