Canonical Allele Identifier: CA980962167

Gene: CXCL16

Linked Data

• gnomAD v3: 17-4734385-G-GTTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGT
• gnomAD v4: 17-4734385-G-GTTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734386_4734387insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTT , CM000679.2:g.4734386_4734387insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTT	GRCh38
NC_000017.10:g.4637681_4637682insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTT , CM000679.1:g.4637681_4637682insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTT	GRCh37
NC_000017.9:g.4584430_4584431insTTGCCTGTGTCCCCACCCAAATCTCATCTTGAATTCTCACGTGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAAA MANE Select	ENSP00000293778.7:n.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGG...
ENST00000574412.6:c.*220_*221insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAAA	ENSP00000459592.2:n.*220_*221insACACGTGAGAATTCAAGATGAGATTTGGG...
ENST00000293778.10:c.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAAA	ENSP00000293778.6:n.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGG...
ENST00000574412.5:c.*220_*221insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAAA	ENSP00000459592.1:n.*220_*221insACACGTGAGAATTCAAGATGAGATTTGGG...
ENST00000576153.5:n.673_674insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAAA
NM_022059.3:c.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAAA	NP_071342.2:n.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGA...
NM_022059.4:c.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAAA	NP_071342.2:n.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGA...
NM_001386809.1:c.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGGTGGGGACACAGGCAAA MANE Select	NP_001373738.1:n.*117_*118insACACGTGAGAATTCAAGATGAGATTTGGGTGG...