Canonical Allele Identifier: CA2646116099
Gene: SLC35D1 HGNC NCBI

Linked Data

gnomAD v4: 1-67009278-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009278A>G , CM000663.2:g.67009278A>G GRCh38
NC_000001.10:g.67474961A>G , CM000663.1:g.67474961A>G GRCh37
NC_000001.9:g.67247549A>G NCBI36
NG_012933.1:g.50120T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-111T>C MANE Select ENSP00000235345.5:n.877-111T>C
ENST00000235345.5:c.877-111T>C ENSP00000235345.5:n.877-111T>C
NM_015139.2:c.877-111T>C NP_055954.1:n.877-111T>C
XM_006710478.1:c.958-111T>C XP_006710541.1:n.958-111T>C
XM_011541070.1:c.958-111T>C XP_011539372.1:n.958-111T>C
XM_006710478.2:c.958-111T>C XP_006710541.1:n.958-111T>C
XM_011541070.2:c.958-111T>C XP_011539372.1:n.958-111T>C
XR_001737057.2:n.1461-111T>C
XR_001737058.2:n.2246-111T>C
NM_015139.3:c.877-111T>C MANE Select NP_055954.1:n.877-111T>C
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