Canonical Allele Identifier: CA2671053009

Linked Data

gnomAD v4: 4-76021794-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76021794G>T , CM000666.2:g.76021794G>T GRCh38
NC_000004.11:g.76942947G>T , CM000666.1:g.76942947G>T GRCh37
NC_000004.10:g.77161971G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306602.3:c.*136C>A (CXCL10) MANE Select ENSP00000305651.1:n.*136C>A
ENST00000306602.2:c.*136C>A (CXCL10) ENSP00000305651.1:n.*136C>A
ENST00000341029.9:c.-10+10474G>T (ART3) ENSP00000343843.5:n.-10+10474G>T
ENST00000504914.5:c.-10+9551G>T (ART3) ENSP00000421431.1:n.-10+9551G>T
ENST00000510669.5:n.121+10474G>T (ART3)
ENST00000513122.5:c.-125+10474G>T (ART3) ENSP00000422287.1:n.-125+10474G>T
ENST00000513353.5:c.-44+10474G>T (ART3) ENSP00000421345.1:n.-44+10474G>T
NM_001130017.2:c.-10+10474G>T (ART3) NP_001123489.1:n.-10+10474G>T
NM_001565.3:c.*136C>A (CXCL10) NP_001556.2:n.*136C>A
XM_017008206.2:c.-44+10474G>T (ART3) XP_016863695.1:n.-44+10474G>T
XM_024454051.1:c.-10+10474G>T (ART3) XP_024309819.1:n.-10+10474G>T
XM_024454052.1:c.-125+10474G>T (ART3) XP_024309820.1:n.-125+10474G>T
XM_024454053.1:c.-136+10474G>T (ART3) XP_024309821.1:n.-136+10474G>T
XM_024454063.1:c.-10+10474G>T (ART3) XP_024309831.1:n.-10+10474G>T
NM_001565.4:c.*136C>A (CXCL10) MANE Select NP_001556.2:n.*136C>A
NM_001130017.3:c.-10+10474G>T (ART3) NP_001123489.1:n.-10+10474G>T
NM_001377177.1:c.-10+10474G>T (ART3) NP_001364106.1:n.-10+10474G>T
NM_001377181.1:c.-10+10474G>T (ART3) NP_001364110.1:n.-10+10474G>T
NM_001377183.1:c.-10+10474G>T (ART3) NP_001364112.1:n.-10+10474G>T
NR_168520.1:n.372C>A (CXCL10)