Canonical Allele Identifier: CA2576144210

Gene: SLC13A5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695985G>A , CM000679.2:g.6695985G>A	GRCh38
NC_000017.10:g.6599304G>A , CM000679.1:g.6599304G>A	GRCh37
NC_000017.9:g.6540028G>A	NCBI36
NG_034220.1:g.22437C>T , LRG_1020:g.22437C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.840-44C>T MANE Select	ENSP00000406220.2:n.840-44C>T
ENST00000293800.10:c.789-44C>T	ENSP00000293800.6:n.789-44C>T
ENST00000381074.8:c.711-44C>T	ENSP00000370464.4:n.711-44C>T
ENST00000433363.6:c.840-44C>T	ENSP00000406220.2:n.840-44C>T
ENST00000572094.1:c.*590-44C>T	ENSP00000461495.1:n.*590-44C>T
ENST00000573648.5:c.840-44C>T	ENSP00000459372.1:n.840-44C>T
ENST00000574824.5:n.1973-44C>T
NM_001143838.2:c.840-44C>T	NP_001137310.1:n.840-44C>T
NM_001284509.1:c.789-44C>T	NP_001271438.1:n.789-44C>T
NM_001284510.1:c.711-44C>T	NP_001271439.1:n.711-44C>T
NM_177550.4:c.840-44C>T , LRG_1020t1:c.840-44C>T	NP_808218.1:n.840-44C>T
XM_006721504.2:c.729-44C>T	XP_006721567.1:n.729-44C>T
XM_011523795.1:c.840-44C>T	XP_011522097.1:n.840-44C>T
XM_011523795.3:c.840-44C>T	XP_011522097.1:n.840-44C>T
NM_001143838.3:c.840-44C>T	NP_001137310.1:n.840-44C>T
NM_001284509.2:c.789-44C>T	NP_001271438.1:n.789-44C>T
NM_001284510.2:c.711-44C>T	NP_001271439.1:n.711-44C>T
NM_177550.5:c.840-44C>T MANE Select	NP_808218.1:n.840-44C>T