Canonical Allele Identifier: CA2560797381
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009283_67009284insTA , CM000663.2:g.67009283_67009284insTA GRCh38
NC_000001.10:g.67474966_67474967insTA , CM000663.1:g.67474966_67474967insTA GRCh37
NC_000001.9:g.67247554_67247555insTA NCBI36
NG_012933.1:g.50115_50116insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-116_877-115insAT MANE Select ENSP00000235345.5:n.877-116_877-115insAT
ENST00000235345.5:c.877-116_877-115insAT ENSP00000235345.5:n.877-116_877-115insAT
NM_015139.2:c.877-116_877-115insAT NP_055954.1:n.877-116_877-115insAT
XM_006710478.1:c.958-116_958-115insAT XP_006710541.1:n.958-116_958-115insAT
XM_011541070.1:c.958-116_958-115insAT XP_011539372.1:n.958-116_958-115insAT
XM_006710478.2:c.958-116_958-115insAT XP_006710541.1:n.958-116_958-115insAT
XM_011541070.2:c.958-116_958-115insAT XP_011539372.1:n.958-116_958-115insAT
XR_001737057.2:n.1461-116_1461-115insAT
XR_001737058.2:n.2246-116_2246-115insAT
NM_015139.3:c.877-116_877-115insAT MANE Select NP_055954.1:n.877-116_877-115insAT