Canonical Allele Identifier: CA357304172

Gene: CXCL10 ART3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76022721G>A , CM000666.2:g.76022721G>A	GRCh38
NC_000004.11:g.76943874G>A , CM000666.1:g.76943874G>A	GRCh37
NC_000004.10:g.77162898G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001565.4:c.158C>T (CXCL10) MANE Select	NP_001556.2:p.Ala53Val
ENST00000306602.3:c.158C>T (CXCL10) MANE Select	ENSP00000305651.1:p.Ala53Val
NM_001130017.2:c.-10+11401G>A (ART3)	NP_001123489.1:n.-10+11401G>A
NM_001130017.3:c.-10+11401G>A (ART3)	NP_001123489.1:n.-10+11401G>A
NM_001377177.1:c.-10+11401G>A (ART3)	NP_001364106.1:n.-10+11401G>A
NM_001377181.1:c.-10+11401G>A (ART3)	NP_001364110.1:n.-10+11401G>A
NM_001377183.1:c.-10+11401G>A (ART3)	NP_001364112.1:n.-10+11401G>A
NM_001565.3:c.158C>T (CXCL10)	NP_001556.2:p.Ala53Val
NR_168520.1:n.128-266C>T (CXCL10)
ENST00000306602.2:c.158C>T (CXCL10)	ENSP00000305651.1:p.Ala53Val
ENST00000341029.9:c.-10+11401G>A (ART3)	ENSP00000343843.5:n.-10+11401G>A
ENST00000504914.5:c.-10+10478G>A (ART3)	ENSP00000421431.1:n.-10+10478G>A
ENST00000510669.5:n.121+11401G>A (ART3)
ENST00000513122.5:c.-125+11401G>A (ART3)	ENSP00000422287.1:n.-125+11401G>A
ENST00000513353.5:c.-44+11401G>A (ART3)	ENSP00000421345.1:n.-44+11401G>A
XM_017008206.2:c.-44+11401G>A (ART3)	XP_016863695.1:n.-44+11401G>A
XM_024454051.1:c.-10+11401G>A (ART3)	XP_024309819.1:n.-10+11401G>A
XM_024454052.1:c.-125+11401G>A (ART3)	XP_024309820.1:n.-125+11401G>A
XM_024454053.1:c.-136+11401G>A (ART3)	XP_024309821.1:n.-136+11401G>A
XM_024454063.1:c.-10+11401G>A (ART3)	XP_024309831.1:n.-10+11401G>A