Canonical Allele Identifier: CA99820358

Gene: CXCL10 ART3

Linked Data

• dbSNP Id: rs999975208
• gnomAD v4: 4-76021808-G-T
• MyVariant Identifiers: chr4:g.76942961G>T (hg19) ; chr4:g.76021808G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76021808G>T , CM000666.2:g.76021808G>T	GRCh38
NC_000004.11:g.76942961G>T , CM000666.1:g.76942961G>T	GRCh37
NC_000004.10:g.77161985G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306602.3:c.*122C>A (CXCL10) MANE Select	ENSP00000305651.1:n.*122C>A
ENST00000306602.2:c.*122C>A (CXCL10)	ENSP00000305651.1:n.*122C>A
ENST00000341029.9:c.-10+10488G>T (ART3)	ENSP00000343843.5:n.-10+10488G>T
ENST00000504914.5:c.-10+9565G>T (ART3)	ENSP00000421431.1:n.-10+9565G>T
ENST00000510669.5:n.121+10488G>T (ART3)
ENST00000513122.5:c.-125+10488G>T (ART3)	ENSP00000422287.1:n.-125+10488G>T
ENST00000513353.5:c.-44+10488G>T (ART3)	ENSP00000421345.1:n.-44+10488G>T
NM_001130017.2:c.-10+10488G>T (ART3)	NP_001123489.1:n.-10+10488G>T
NM_001565.3:c.*122C>A (CXCL10)	NP_001556.2:n.*122C>A
XM_017008206.2:c.-44+10488G>T (ART3)	XP_016863695.1:n.-44+10488G>T
XM_024454051.1:c.-10+10488G>T (ART3)	XP_024309819.1:n.-10+10488G>T
XM_024454052.1:c.-125+10488G>T (ART3)	XP_024309820.1:n.-125+10488G>T
XM_024454053.1:c.-136+10488G>T (ART3)	XP_024309821.1:n.-136+10488G>T
XM_024454063.1:c.-10+10488G>T (ART3)	XP_024309831.1:n.-10+10488G>T
NM_001565.4:c.*122C>A (CXCL10) MANE Select	NP_001556.2:n.*122C>A
NM_001130017.3:c.-10+10488G>T (ART3)	NP_001123489.1:n.-10+10488G>T
NM_001377177.1:c.-10+10488G>T (ART3)	NP_001364106.1:n.-10+10488G>T
NM_001377181.1:c.-10+10488G>T (ART3)	NP_001364110.1:n.-10+10488G>T
NM_001377183.1:c.-10+10488G>T (ART3)	NP_001364112.1:n.-10+10488G>T
NR_168520.1:n.358C>A (CXCL10)