Canonical Allele Identifier: CA1658070443
Gene: SLC35F1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.118297827G= , CM000668.2:g.118297827G= GRCh38
NC_000006.11:g.118618990G= , CM000668.1:g.118618990G= GRCh37
NC_000006.10:g.118725683G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360388.9:c.1002+12489G= MANE Select ENSP00000353557.4:n.1002+12489G=
ENST00000360388.8:c.1002+12489G= ENSP00000353557.4:n.1002+12489G=
ENST00000621341.1:c.825+12489G= ENSP00000484738.1:n.825+12489G=
NM_001029858.3:c.1002+12489G= NP_001025029.2:n.1002+12489G=
XM_005266865.3:c.1002+12489G= XP_005266922.1:n.1002+12489G=
XR_942913.1:n.342-7317C=
XM_005266865.4:c.1002+12489G= XP_005266922.1:n.1002+12489G=
NM_001029858.4:c.1002+12489G= MANE Select NP_001025029.2:n.1002+12489G=
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