Canonical Allele Identifier: CA1658070454
Gene: SLC35F1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.118297870A= , CM000668.2:g.118297870A= GRCh38
NC_000006.11:g.118619033A= , CM000668.1:g.118619033A= GRCh37
NC_000006.10:g.118725726A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360388.9:c.1002+12532A= MANE Select ENSP00000353557.4:n.1002+12532A=
ENST00000360388.8:c.1002+12532A= ENSP00000353557.4:n.1002+12532A=
ENST00000621341.1:c.825+12532A= ENSP00000484738.1:n.825+12532A=
NM_001029858.3:c.1002+12532A= NP_001025029.2:n.1002+12532A=
XM_005266865.3:c.1002+12532A= XP_005266922.1:n.1002+12532A=
XR_942913.1:n.342-7360T=
XM_005266865.4:c.1002+12532A= XP_005266922.1:n.1002+12532A=
NM_001029858.4:c.1002+12532A= MANE Select NP_001025029.2:n.1002+12532A=
Search 100 bp 5'
Search 100 bp 3'