Canonical Allele Identifier: CA7718935

Gene: ISG20

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88639588G>C , CM000677.2:g.88639588G>C	GRCh38
NC_000015.9:g.89182819G>C , CM000677.1:g.89182819G>C	GRCh37
NC_000015.8:g.86983823G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306072.10:c.222G>C MANE Select	ENSP00000306565.5:p.Arg74Ser
ENST00000379224.10:c.222G>C	ENSP00000368526.6:p.Arg74Ser
ENST00000558942.6:n.360G>C
ENST00000559876.2:c.222G>C	ENSP00000453666.2:p.Arg74Ser
ENST00000306072.9:c.222G>C	ENSP00000306565.5:p.Arg74Ser
ENST00000379224.9:c.222G>C	ENSP00000368526.5:p.Arg74Ser
ENST00000558942.5:n.360G>C
ENST00000559876.1:c.222G>C	ENSP00000453666.1:p.Arg74Ser
ENST00000560573.1:n.382G>C
ENST00000560741.5:c.222G>C	ENSP00000453638.1:p.Arg74Ser
NM_001303233.1:c.222G>C	NP_001290162.1:p.Arg74Ser
NM_001303234.1:c.222G>C	NP_001290163.1:p.Arg74Ser
NM_001303235.1:c.-1681+3888G>C	NP_001290164.1:n.-1681+3888G>C
NM_001303236.1:c.-1687G>C	NP_001290165.1:n.-1687G>C
NM_001303237.1:c.222G>C	NP_001290166.1:p.Arg74Ser
NM_002201.5:c.222G>C	NP_002192.2:p.Arg74Ser
NR_130134.1:n.64+3888G>C
XM_005254899.1:c.222G>C	XP_005254956.1:p.Arg74Ser
XM_006720488.2:c.222G>C	XP_006720551.1:p.Arg74Ser
XM_005254899.2:c.222G>C	XP_005254956.1:p.Arg74Ser
XM_006720488.3:c.222G>C	XP_006720551.1:p.Arg74Ser
XM_017022147.1:c.-1687G>C	XP_016877636.1:n.-1687G>C
XM_017022148.1:c.222G>C	XP_016877637.1:p.Arg74Ser
NM_002201.6:c.222G>C MANE Select	NP_002192.2:p.Arg74Ser
NM_001303233.2:c.222G>C	NP_001290162.1:p.Arg74Ser
NM_001303234.2:c.222G>C	NP_001290163.1:p.Arg74Ser
NM_001303235.2:c.-1681+3888G>C	NP_001290164.1:n.-1681+3888G>C
NM_001303236.2:c.-1687G>C	NP_001290165.1:n.-1687G>C
NM_001303237.2:c.222G>C	NP_001290166.1:p.Arg74Ser
NR_130134.2:n.69+3888G>C