Canonical Allele Identifier: CA2646115995
Gene: SLC35D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009078dup , CM000663.2:g.67009078dup GRCh38
NC_000001.10:g.67474761dup , CM000663.1:g.67474761dup GRCh37
NC_000001.9:g.67247349dup NCBI36
NG_012933.1:g.50324dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.959+11dup MANE Select ENSP00000235345.5:n.959+11dup
ENST00000235345.5:c.959+11dup ENSP00000235345.5:n.959+11dup
NM_015139.2:c.959+11dup NP_055954.1:n.959+11dup
XM_006710478.1:c.1040+11dup XP_006710541.1:n.1040+11dup
XM_011541070.1:c.1040+11dup XP_011539372.1:n.1040+11dup
XM_006710478.2:c.1040+11dup XP_006710541.1:n.1040+11dup
XM_011541070.2:c.1040+11dup XP_011539372.1:n.1040+11dup
XR_001737057.2:n.1543+11dup
XR_001737058.2:n.2328+11dup
NM_015139.3:c.959+11dup MANE Select NP_055954.1:n.959+11dup