Canonical Allele Identifier: CA606796791
Gene: SLC25A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98595421_98595424del , CM000674.2:g.98595421_98595424del GRCh38
NC_000012.11:g.98989199_98989202del , CM000674.1:g.98989199_98989202del GRCh37
NC_000012.10:g.97513330_97513333del NCBI36
NG_011702.1:g.6797_6800del

Transcript Alleles

HGVS Amino-acid Change
ENST00000228318.8:c.158-12_158-9del MANE Plus Clinical ENSP00000228318.3:n.158-12_158-9del
ENST00000552981.6:c.158-306_158-303del MANE Select ENSP00000448708.2:n.158-306_158-303del
ENST00000188376.9:c.158-306_158-303del ENSP00000188376.5:n.158-306_158-303del
ENST00000228318.7:c.158-12_158-9del ENSP00000228318.3:n.158-12_158-9del
ENST00000401722.7:c.158-306_158-303del ENSP00000383898.3:n.158-306_158-303del
ENST00000546766.5:n.1533_1536del
ENST00000547534.5:c.158-306_158-303del ENSP00000449793.1:n.158-306_158-303del
ENST00000548046.5:c.158-12_158-9del ENSP00000447339.1:n.158-12_158-9del
ENST00000548847.1:c.158-306_158-303del ENSP00000449166.1:n.158-306_158-303del
ENST00000549338.5:c.158-306_158-303del ENSP00000447740.1:n.158-306_158-303del
ENST00000550695.1:c.158-12_158-9del ENSP00000449479.1:n.158-12_158-9del
ENST00000551123.5:c.158-12_158-9del ENSP00000449009.1:n.158-12_158-9del
ENST00000551917.5:c.158-12_158-9del ENSP00000447310.1:n.158-12_158-9del
ENST00000552981.5:c.158-306_158-303del ENSP00000448708.1:n.158-306_158-303del
NM_002635.3:c.158-306_158-303del NP_002626.1:n.158-306_158-303del
NM_005888.3:c.158-12_158-9del NP_005879.1:n.158-12_158-9del
NM_213611.2:c.158-306_158-303del NP_998776.1:n.158-306_158-303del
NM_002635.4:c.158-306_158-303del MANE Select NP_002626.1:n.158-306_158-303del
NM_213611.3:c.158-306_158-303del NP_998776.1:n.158-306_158-303del
NM_005888.4:c.158-12_158-9del MANE Plus Clinical NP_005879.1:n.158-12_158-9del