Canonical Allele Identifier: CA772506979
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1353778297
gnomAD v4: 17-4734255-GTTA-G
MyVariant Identifiers: chr17:g.4637551_4637553del (hg19) chr17:g.4734256_4734258del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734260_4734262del , CM000679.2:g.4734260_4734262del GRCh38
NC_000017.10:g.4637555_4637557del , CM000679.1:g.4637555_4637557del GRCh37
NC_000017.9:g.4584304_4584306del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*245_*247del MANE Select ENSP00000293778.7:n.*245_*247del
ENST00000293778.10:c.*245_*247del ENSP00000293778.6:n.*245_*247del
ENST00000576153.5:n.801_803del
NM_022059.3:c.*245_*247del NP_071342.2:n.*245_*247del
NM_022059.4:c.*245_*247del NP_071342.2:n.*245_*247del
NM_001386809.1:c.*245_*247del MANE Select NP_001373738.1:n.*245_*247del
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