Canonical Allele Identifier: CA2807175669
Gene: CX3CL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57376046A>C , CM000678.2:g.57376046A>C GRCh38
NC_000016.9:g.57409958A>C , CM000678.1:g.57409958A>C GRCh37
NC_000016.8:g.55967459A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000006053.7:c.70+3408A>C MANE Select ENSP00000006053.6:n.70+3408A>C
ENST00000006053.6:c.70+3408A>C ENSP00000006053.6:n.70+3408A>C
ENST00000563383.1:c.70+3408A>C ENSP00000456830.1:n.70+3408A>C
ENST00000564948.1:c.70+3408A>C ENSP00000457996.1:n.70+3408A>C
NM_001304392.1:c.-65+3408A>C NP_001291321.1:n.-65+3408A>C
NM_002996.4:c.70+3408A>C NP_002987.1:n.70+3408A>C
NM_001304392.2:c.-65+3408A>C NP_001291321.1:n.-65+3408A>C
NM_002996.5:c.70+3408A>C NP_002987.1:n.70+3408A>C
NM_002996.6:c.70+3408A>C MANE Select NP_002987.1:n.70+3408A>C
NM_001304392.3:c.-65+3408A>C NP_001291321.1:n.-65+3408A>C