Canonical Allele Identifier: CA774276114
Gene: SLC13A5 HGNC NCBI

Linked Data

dbSNP Id: rs1345470883

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6703612_6703615del , CM000679.2:g.6703612_6703615del GRCh38
NC_000017.10:g.6606931_6606934del , CM000679.1:g.6606931_6606934del GRCh37
NC_000017.9:g.6547655_6547658del NCBI36
NG_034220.1:g.14808_14811del , LRG_1020:g.14808_14811del

Transcript Alleles

HGVS Amino-acid change
ENST00000433363.7:c.547+264_547+267del MANE Select ENSP00000406220.2:n.547+264_547+267del
ENST00000293800.10:c.496+264_496+267del ENSP00000293800.6:n.496+264_496+267del
ENST00000381074.8:c.418+264_418+267del ENSP00000370464.4:n.418+264_418+267del
ENST00000433363.6:c.547+264_547+267del ENSP00000406220.2:n.547+264_547+267del
ENST00000572094.1:c.*297+264_*297+267del ENSP00000461495.1:n.*297+264_*297+267del
ENST00000572352.5:c.436+264_436+267del ENSP00000461622.1:n.436+264_436+267del
ENST00000573648.5:c.547+264_547+267del ENSP00000459372.1:n.547+264_547+267del
ENST00000574824.5:n.1680+264_1680+267del
NM_001143838.2:c.547+264_547+267del NP_001137310.1:n.547+264_547+267del
NM_001284509.1:c.496+264_496+267del NP_001271438.1:n.496+264_496+267del
NM_001284510.1:c.418+264_418+267del NP_001271439.1:n.418+264_418+267del
NM_177550.4:c.547+264_547+267del , LRG_1020t1:c.547+264_547+267del NP_808218.1:n.547+264_547+267del
XM_006721504.2:c.436+264_436+267del XP_006721567.1:n.436+264_436+267del
XM_011523795.1:c.547+264_547+267del XP_011522097.1:n.547+264_547+267del
XM_011523795.3:c.547+264_547+267del XP_011522097.1:n.547+264_547+267del
NM_001143838.3:c.547+264_547+267del NP_001137310.1:n.547+264_547+267del
NM_001284509.2:c.496+264_496+267del NP_001271438.1:n.496+264_496+267del
NM_001284510.2:c.418+264_418+267del NP_001271439.1:n.418+264_418+267del
NM_177550.5:c.547+264_547+267del MANE Select NP_808218.1:n.547+264_547+267del