Canonical Allele Identifier: CA1727517727
Gene: SLC25A13 HGNC NCBI

Linked Data

dbSNP Id: rs1791510981

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96121645_96121663del , CM000669.2:g.96121645_96121663del GRCh38
NC_000007.13:g.95750957_95750975del , CM000669.1:g.95750957_95750975del GRCh37
NC_000007.12:g.95588893_95588911del NCBI36
NG_012247.1:g.205487_205505del
NG_012247.2:g.205487_205505del

Transcript Alleles

HGVS Amino-acid change
ENST00000265631.10:c.1835_1841+12del
ENST00000265631.9:c.1835_1841+12del
ENST00000416240.6:c.1838_1844+12del
ENST00000494085.1:n.338_344+12del
NM_001160210.1:c.1838_1844+12del
NM_014251.2:c.1835_1841+12del
NR_027662.1:n.1910_1916+12del
XM_006715831.2:c.1868_1874+12del
XM_011515728.1:c.983_989+12del
XM_006715831.4:c.1868_1874+12del
XM_017011663.1:c.1826_1832+12del
XM_017011664.2:c.983_989+12del
XM_017011665.1:c.983_989+12del
XR_001744525.2:n.2081_2087+12del
XR_002956405.1:n.2639_2645+12del
NM_014251.3:c.1835_1841+12del
NR_027662.2:n.1861_1867+12del
NM_001160210.2:c.1838_1844+12del