Canonical Allele Identifier: CA1469420503

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76021874A= , CM000666.2:g.76021874A= GRCh38
NC_000004.11:g.76943027A= , CM000666.1:g.76943027A= GRCh37
NC_000004.10:g.77162051A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306602.3:c.*56T= (CXCL10) MANE Select ENSP00000305651.1:n.*56T=
ENST00000306602.2:c.*56T= (CXCL10) ENSP00000305651.1:n.*56T=
ENST00000341029.9:c.-10+10554A= (ART3) ENSP00000343843.5:n.-10+10554A=
ENST00000504914.5:c.-10+9631A= (ART3) ENSP00000421431.1:n.-10+9631A=
ENST00000510669.5:n.121+10554A= (ART3)
ENST00000513122.5:c.-125+10554A= (ART3) ENSP00000422287.1:n.-125+10554A=
ENST00000513353.5:c.-44+10554A= (ART3) ENSP00000421345.1:n.-44+10554A=
NM_001130017.2:c.-10+10554A= (ART3) NP_001123489.1:n.-10+10554A=
NM_001565.3:c.*56T= (CXCL10) NP_001556.2:n.*56T=
XM_017008206.2:c.-44+10554A= (ART3) XP_016863695.1:n.-44+10554A=
XM_024454051.1:c.-10+10554A= (ART3) XP_024309819.1:n.-10+10554A=
XM_024454052.1:c.-125+10554A= (ART3) XP_024309820.1:n.-125+10554A=
XM_024454053.1:c.-136+10554A= (ART3) XP_024309821.1:n.-136+10554A=
XM_024454063.1:c.-10+10554A= (ART3) XP_024309831.1:n.-10+10554A=
NM_001565.4:c.*56T= (CXCL10) MANE Select NP_001556.2:n.*56T=
NM_001130017.3:c.-10+10554A= (ART3) NP_001123489.1:n.-10+10554A=
NM_001377177.1:c.-10+10554A= (ART3) NP_001364106.1:n.-10+10554A=
NM_001377181.1:c.-10+10554A= (ART3) NP_001364110.1:n.-10+10554A=
NM_001377183.1:c.-10+10554A= (ART3) NP_001364112.1:n.-10+10554A=
NR_168520.1:n.292T= (CXCL10)