Canonical Allele Identifier: CA360694343
Gene: SLC25A46 HGNC NCBI

Linked Data

COSMIC: COSM6197129
MyVariant Identifiers: chr5:g.110081971T>C (hg19) chr5:g.110746270T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.110746270T>C , CM000667.2:g.110746270T>C GRCh38
NC_000005.9:g.110081971T>C , CM000667.1:g.110081971T>C GRCh37
NC_000005.8:g.110109870T>C NCBI36
NG_051334.1:g.13135T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000355943.8:c.386T>C MANE Select ENSP00000348211.3:p.Val129Ala
ENST00000355943.7:c.386T>C ENSP00000348211.3:p.Val129Ala
ENST00000447245.6:c.386T>C ENSP00000399717.2:p.Val129Ala
ENST00000502462.6:n.702T>C
ENST00000504098.1:c.-53T>C ENSP00000425708.1:n.-53T>C
ENST00000508781.5:n.215T>C
ENST00000513807.5:c.-101T>C ENSP00000421134.1:n.-101T>C
NM_001303249.1:c.386T>C NP_001290178.1:p.Val129Ala
NM_001303250.1:c.113T>C NP_001290179.1:p.Val38Ala
NM_138773.2:c.386T>C NP_620128.1:p.Val129Ala
XM_011543708.1:c.386T>C XP_011542010.1:p.Val129Ala
NM_001303249.2:c.386T>C NP_001290178.1:p.Val129Ala
NM_001303250.2:c.113T>C NP_001290179.1:p.Val38Ala
NM_138773.3:c.386T>C NP_620128.1:p.Val129Ala
NR_138151.1:n.534T>C
NM_138773.4:c.386T>C MANE Select NP_620128.1:p.Val129Ala
NM_001303249.3:c.386T>C NP_001290178.1:p.Val129Ala
NM_001303250.3:c.113T>C NP_001290179.1:p.Val38Ala
NR_138151.2:n.499T>C
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