Canonical Allele Identifier: CA2646116089
Gene: SLC35D1 HGNC NCBI

Linked Data

gnomAD v4: 1-67009270-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009270T>G , CM000663.2:g.67009270T>G GRCh38
NC_000001.10:g.67474953T>G , CM000663.1:g.67474953T>G GRCh37
NC_000001.9:g.67247541T>G NCBI36
NG_012933.1:g.50128A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-103A>C MANE Select ENSP00000235345.5:n.877-103A>C
ENST00000235345.5:c.877-103A>C ENSP00000235345.5:n.877-103A>C
NM_015139.2:c.877-103A>C NP_055954.1:n.877-103A>C
XM_006710478.1:c.958-103A>C XP_006710541.1:n.958-103A>C
XM_011541070.1:c.958-103A>C XP_011539372.1:n.958-103A>C
XM_006710478.2:c.958-103A>C XP_006710541.1:n.958-103A>C
XM_011541070.2:c.958-103A>C XP_011539372.1:n.958-103A>C
XR_001737057.2:n.1461-103A>C
XR_001737058.2:n.2246-103A>C
NM_015139.3:c.877-103A>C MANE Select NP_055954.1:n.877-103A>C