Canonical Allele Identifier: CA340708585
Gene: SLC35D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053898A>C , CM000663.2:g.67053898A>C GRCh38
NC_000001.10:g.67519581A>C , CM000663.1:g.67519581A>C GRCh37
NC_000001.9:g.67292169A>C NCBI36
NG_012933.1:g.5500T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.116T>G MANE Select ENSP00000235345.5:p.Val39Gly
ENST00000235345.5:c.116T>G ENSP00000235345.5:p.Val39Gly
NM_015139.2:c.116T>G NP_055954.1:p.Val39Gly
XM_006710478.1:c.116T>G XP_006710541.1:p.Val39Gly
XM_011541070.1:c.116T>G XP_011539372.1:p.Val39Gly
XM_006710478.2:c.116T>G XP_006710541.1:p.Val39Gly
XM_011541070.2:c.116T>G XP_011539372.1:p.Val39Gly
XR_001737057.2:n.526T>G
XR_001737058.2:n.519T>G
NM_015139.3:c.116T>G MANE Select NP_055954.1:p.Val39Gly