Canonical Allele Identifier: CA651061853
Gene: SLC35F1 HGNC NCBI

Linked Data

COSMIC: COSN7595961
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.118297852G>A , CM000668.2:g.118297852G>A GRCh38
NC_000006.11:g.118619015G>A , CM000668.1:g.118619015G>A GRCh37
NC_000006.10:g.118725708G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360388.9:c.1002+12514G>A MANE Select ENSP00000353557.4:n.1002+12514G>A
ENST00000360388.8:c.1002+12514G>A ENSP00000353557.4:n.1002+12514G>A
ENST00000621341.1:c.825+12514G>A ENSP00000484738.1:n.825+12514G>A
NM_001029858.3:c.1002+12514G>A NP_001025029.2:n.1002+12514G>A
XM_005266865.3:c.1002+12514G>A XP_005266922.1:n.1002+12514G>A
XR_942913.1:n.342-7342C>T
XM_005266865.4:c.1002+12514G>A XP_005266922.1:n.1002+12514G>A
NM_001029858.4:c.1002+12514G>A MANE Select NP_001025029.2:n.1002+12514G>A
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