Canonical Allele Identifier: CA1658070369
Gene: SLC35F1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.118297725T= , CM000668.2:g.118297725T= GRCh38
NC_000006.11:g.118618888T= , CM000668.1:g.118618888T= GRCh37
NC_000006.10:g.118725581T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360388.9:c.1002+12387T= MANE Select ENSP00000353557.4:n.1002+12387T=
ENST00000360388.8:c.1002+12387T= ENSP00000353557.4:n.1002+12387T=
ENST00000621341.1:c.825+12387T= ENSP00000484738.1:n.825+12387T=
NM_001029858.3:c.1002+12387T= NP_001025029.2:n.1002+12387T=
XM_005266865.3:c.1002+12387T= XP_005266922.1:n.1002+12387T=
XR_942913.1:n.342-7215A=
XM_005266865.4:c.1002+12387T= XP_005266922.1:n.1002+12387T=
NM_001029858.4:c.1002+12387T= MANE Select NP_001025029.2:n.1002+12387T=
Search 100 bp 5'
Search 100 bp 3'