Canonical Allele Identifier: CA397738347

Gene: SLC13A5 C17orf100 ALOX15P1

Linked Data

• MyVariant Identifiers: chr17:g.6590943A>C (hg19) ; chr17:g.6687624A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6687624A>C , CM000679.2:g.6687624A>C	GRCh38
NC_000017.10:g.6590943A>C , CM000679.1:g.6590943A>C	GRCh37
NC_000017.9:g.6531667A>C	NCBI36
NG_034220.1:g.30798T>G , LRG_1020:g.30798T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.1480T>G (SLC13A5) MANE Select	ENSP00000406220.2:p.Cys494Gly
ENST00000635042.1:n.725-5241A>C (C17orf100)
ENST00000293800.10:c.1429T>G (SLC13A5)	ENSP00000293800.6:p.Cys477Gly
ENST00000381074.8:c.1351T>G (SLC13A5)	ENSP00000370464.4:p.Cys451Gly
ENST00000433363.6:c.1480T>G (SLC13A5)	ENSP00000406220.2:p.Cys494Gly
ENST00000570687.1:c.149T>G (SLC13A5)
ENST00000573648.5:c.1438-1286T>G (SLC13A5)	ENSP00000459372.1:n.1438-1286T>G
ENST00000574580.2:n.2497T>G (SLC13A5)
ENST00000634558.1:n.511-2252A>C (ALOX15P1)
ENST00000634823.1:n.265-5241A>C (ALOX15P1)
NM_001143838.2:c.1438-1286T>G (SLC13A5)	NP_001137310.1:n.1438-1286T>G
NM_001284509.1:c.1429T>G (SLC13A5)	NP_001271438.1:p.Cys477Gly
NM_001284510.1:c.1351T>G (SLC13A5)	NP_001271439.1:p.Cys451Gly
NM_177550.4:c.1480T>G , LRG_1020t1:c.1480T>G (SLC13A5)	NP_808218.1:p.Cys494Gly
XM_006721504.2:c.1369T>G (SLC13A5)	XP_006721567.1:p.Cys457Gly
XM_011523795.3:c.*153T>G (SLC13A5)	XP_011522097.1:n.*153T>G
NM_001143838.3:c.1438-1286T>G (SLC13A5)	NP_001137310.1:n.1438-1286T>G
NM_001284509.2:c.1429T>G (SLC13A5)	NP_001271438.1:p.Cys477Gly
NM_001284510.2:c.1351T>G (SLC13A5)	NP_001271439.1:p.Cys451Gly
NM_177550.5:c.1480T>G (SLC13A5) MANE Select	NP_808218.1:p.Cys494Gly