Canonical Allele Identifier: CA99825226

Gene: CXCL11 ART3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76035929T>G , CM000666.2:g.76035929T>G	GRCh38
NC_000004.11:g.76957082T>G , CM000666.1:g.76957082T>G	GRCh37
NC_000004.10:g.77176106T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005409.5:c.59A>C (CXCL11) MANE Select	NP_005400.1:p.Gln20Pro
ENST00000306621.8:c.59A>C (CXCL11) MANE Select	ENSP00000306884.3:p.Gln20Pro
NM_001130017.2:c.-10+24609T>G (ART3)	NP_001123489.1:n.-10+24609T>G
NM_001130017.3:c.-10+24609T>G (ART3)	NP_001123489.1:n.-10+24609T>G
NM_001302123.1:c.59A>C (CXCL11)	NP_001289052.1:p.Gln20Pro
NM_001302123.2:c.59A>C (CXCL11)	NP_001289052.1:p.Gln20Pro
NM_001377177.1:c.-10+24609T>G (ART3)	NP_001364106.1:n.-10+24609T>G
NM_001377181.1:c.-10+24609T>G (ART3)	NP_001364110.1:n.-10+24609T>G
NM_001377183.1:c.-10+24609T>G (ART3)	NP_001364112.1:n.-10+24609T>G
NM_005409.4:c.59A>C (CXCL11)	NP_005400.1:p.Gln20Pro
ENST00000306621.7:c.59A>C (CXCL11)	ENSP00000306884.3:p.Gln20Pro
ENST00000341029.9:c.-10+24609T>G (ART3)	ENSP00000343843.5:n.-10+24609T>G
ENST00000503860.1:c.59A>C (CXCL11)	ENSP00000425819.1:p.Gln20Pro
ENST00000504914.5:c.-10+23686T>G (ART3)	ENSP00000421431.1:n.-10+23686T>G
ENST00000510669.5:n.121+24609T>G (ART3)
ENST00000513122.5:c.-124-22061T>G (ART3)	ENSP00000422287.1:n.-124-22061T>G
ENST00000513353.5:c.-43-22663T>G (ART3)	ENSP00000421345.1:n.-43-22663T>G
XM_017008206.2:c.-43-22663T>G (ART3)	XP_016863695.1:n.-43-22663T>G
XM_024454051.1:c.-10+24609T>G (ART3)	XP_024309819.1:n.-10+24609T>G
XM_024454052.1:c.-124-22061T>G (ART3)	XP_024309820.1:n.-124-22061T>G
XM_024454053.1:c.-135-22050T>G (ART3)	XP_024309821.1:n.-135-22050T>G
XM_024454063.1:c.-10+24609T>G (ART3)	XP_024309831.1:n.-10+24609T>G