Canonical Allele Identifier: CA2567592187
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009286_67009288del , CM000663.2:g.67009286_67009288del GRCh38
NC_000001.10:g.67474969_67474971del , CM000663.1:g.67474969_67474971del GRCh37
NC_000001.9:g.67247557_67247559del NCBI36
NG_012933.1:g.50110_50112del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-121_877-119del MANE Select ENSP00000235345.5:n.877-121_877-119del
ENST00000235345.5:c.877-121_877-119del ENSP00000235345.5:n.877-121_877-119del
NM_015139.2:c.877-121_877-119del NP_055954.1:n.877-121_877-119del
XM_006710478.1:c.958-121_958-119del XP_006710541.1:n.958-121_958-119del
XM_011541070.1:c.958-121_958-119del XP_011539372.1:n.958-121_958-119del
XM_006710478.2:c.958-121_958-119del XP_006710541.1:n.958-121_958-119del
XM_011541070.2:c.958-121_958-119del XP_011539372.1:n.958-121_958-119del
XR_001737057.2:n.1461-121_1461-119del
XR_001737058.2:n.2246-121_2246-119del
NM_015139.3:c.877-121_877-119del MANE Select NP_055954.1:n.877-121_877-119del