Canonical Allele Identifier: CA1172975802
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053965G= , CM000663.2:g.67053965G= GRCh38
NC_000001.10:g.67519648G= , CM000663.1:g.67519648G= GRCh37
NC_000001.9:g.67292236G= NCBI36
NG_012933.1:g.5433C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.49C= MANE Select ENSP00000235345.5:p.Pro17=
ENST00000235345.5:c.49C= ENSP00000235345.5:p.Pro17=
NM_015139.2:c.49C= NP_055954.1:p.Pro17=
XM_006710478.1:c.49C= XP_006710541.1:p.Pro17=
XM_011541070.1:c.49C= XP_011539372.1:p.Pro17=
XM_006710478.2:c.49C= XP_006710541.1:p.Pro17=
XM_011541070.2:c.49C= XP_011539372.1:p.Pro17=
XR_001737057.2:n.459C=
XR_001737058.2:n.452C=
NM_015139.3:c.49C= MANE Select NP_055954.1:p.Pro17=