Canonical Allele Identifier: CA1172961686
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009262A= , CM000663.2:g.67009262A= GRCh38
NC_000001.10:g.67474945A= , CM000663.1:g.67474945A= GRCh37
NC_000001.9:g.67247533A= NCBI36
NG_012933.1:g.50136T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-95T= MANE Select ENSP00000235345.5:n.877-95T=
ENST00000235345.5:c.877-95T= ENSP00000235345.5:n.877-95T=
NM_015139.2:c.877-95T= NP_055954.1:n.877-95T=
XM_006710478.1:c.958-95T= XP_006710541.1:n.958-95T=
XM_011541070.1:c.958-95T= XP_011539372.1:n.958-95T=
XM_006710478.2:c.958-95T= XP_006710541.1:n.958-95T=
XM_011541070.2:c.958-95T= XP_011539372.1:n.958-95T=
XR_001737057.2:n.1461-95T=
XR_001737058.2:n.2246-95T=
NM_015139.3:c.877-95T= MANE Select NP_055954.1:n.877-95T=