Canonical Allele Identifier: CA2646116122
Gene: SLC35D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009288_67009289insAAGGTTAG , CM000663.2:g.67009288_67009289insAAGGTTAG GRCh38
NC_000001.10:g.67474971_67474972insAAGGTTAG , CM000663.1:g.67474971_67474972insAAGGTTAG GRCh37
NC_000001.9:g.67247559_67247560insAAGGTTAG NCBI36
NG_012933.1:g.50109_50110insCTAACCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-122_877-121insCTAACCTT MANE Select ENSP00000235345.5:n.877-122_877-121insCTAACCTT
ENST00000235345.5:c.877-122_877-121insCTAACCTT ENSP00000235345.5:n.877-122_877-121insCTAACCTT
NM_015139.2:c.877-122_877-121insCTAACCTT NP_055954.1:n.877-122_877-121insCTAACCTT
XM_006710478.1:c.958-122_958-121insCTAACCTT XP_006710541.1:n.958-122_958-121insCTAACCTT
XM_011541070.1:c.958-122_958-121insCTAACCTT XP_011539372.1:n.958-122_958-121insCTAACCTT
XM_006710478.2:c.958-122_958-121insCTAACCTT XP_006710541.1:n.958-122_958-121insCTAACCTT
XM_011541070.2:c.958-122_958-121insCTAACCTT XP_011539372.1:n.958-122_958-121insCTAACCTT
XR_001737057.2:n.1461-122_1461-121insCTAACCTT
XR_001737058.2:n.2246-122_2246-121insCTAACCTT
NM_015139.3:c.877-122_877-121insCTAACCTT MANE Select NP_055954.1:n.877-122_877-121insCTAACCTT