Canonical Allele Identifier: CA340708770
Gene: SLC35D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053992G>C , CM000663.2:g.67053992G>C GRCh38
NC_000001.10:g.67519675G>C , CM000663.1:g.67519675G>C GRCh37
NC_000001.9:g.67292263G>C NCBI36
NG_012933.1:g.5406C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.22C>G MANE Select ENSP00000235345.5:p.Gln8Glu
ENST00000235345.5:c.22C>G ENSP00000235345.5:p.Gln8Glu
NM_015139.2:c.22C>G NP_055954.1:p.Gln8Glu
XM_006710478.1:c.22C>G XP_006710541.1:p.Gln8Glu
XM_011541070.1:c.22C>G XP_011539372.1:p.Gln8Glu
XM_006710478.2:c.22C>G XP_006710541.1:p.Gln8Glu
XM_011541070.2:c.22C>G XP_011539372.1:p.Gln8Glu
XR_001737057.2:n.432C>G
XR_001737058.2:n.425C>G
NM_015139.3:c.22C>G MANE Select NP_055954.1:p.Gln8Glu