Canonical Allele Identifier: CA2562501767
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054022_67054023del , CM000663.2:g.67054022_67054023del GRCh38
NC_000001.10:g.67519705_67519706del , CM000663.1:g.67519705_67519706del GRCh37
NC_000001.9:g.67292293_67292294del NCBI36
NG_012933.1:g.5375_5376del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-10_-9del MANE Select ENSP00000235345.5:n.-10_-9del
ENST00000235345.5:c.-10_-9del ENSP00000235345.5:n.-10_-9del
NM_015139.2:c.-10_-9del NP_055954.1:n.-10_-9del
XM_006710478.1:c.-10_-9del XP_006710541.1:n.-10_-9del
XM_011541070.1:c.-10_-9del XP_011539372.1:n.-10_-9del
XM_006710478.2:c.-10_-9del XP_006710541.1:n.-10_-9del
XM_011541070.2:c.-10_-9del XP_011539372.1:n.-10_-9del
XR_001737057.2:n.401_402del
XR_001737058.2:n.394_395del
NM_015139.3:c.-10_-9del MANE Select NP_055954.1:n.-10_-9del