Canonical Allele Identifier: CA397750163

Gene: SLC13A5

Linked Data

• MyVariant Identifiers: chr17:g.6607322T>A (hg19) ; chr17:g.6704003T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6704003T>A , CM000679.2:g.6704003T>A	GRCh38
NC_000017.10:g.6607322T>A , CM000679.1:g.6607322T>A	GRCh37
NC_000017.9:g.6548046T>A	NCBI36
NG_034220.1:g.14419A>T , LRG_1020:g.14419A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.422A>T MANE Select	ENSP00000406220.2:p.Asn141Ile
ENST00000293800.10:c.371A>T	ENSP00000293800.6:p.Asn124Ile
ENST00000381074.8:c.293A>T	ENSP00000370464.4:p.Asn98Ile
ENST00000433363.6:c.422A>T	ENSP00000406220.2:p.Asn141Ile
ENST00000572094.1:c.*172A>T	ENSP00000461495.1:n.*172A>T
ENST00000572352.5:c.311A>T	ENSP00000461622.1:p.Asn104Ile
ENST00000573648.5:c.422A>T	ENSP00000459372.1:p.Asn141Ile
ENST00000574824.5:n.1555A>T
ENST00000576323.1:n.452A>T
NM_001143838.2:c.422A>T	NP_001137310.1:p.Asn141Ile
NM_001284509.1:c.371A>T	NP_001271438.1:p.Asn124Ile
NM_001284510.1:c.293A>T	NP_001271439.1:p.Asn98Ile
NM_177550.4:c.422A>T , LRG_1020t1:c.422A>T	NP_808218.1:p.Asn141Ile
XM_006721504.2:c.311A>T	XP_006721567.1:p.Asn104Ile
XM_011523795.1:c.422A>T	XP_011522097.1:p.Asn141Ile
XM_011523795.3:c.422A>T	XP_011522097.1:p.Asn141Ile
NM_001143838.3:c.422A>T	NP_001137310.1:p.Asn141Ile
NM_001284509.2:c.371A>T	NP_001271438.1:p.Asn124Ile
NM_001284510.2:c.293A>T	NP_001271439.1:p.Asn98Ile
NM_177550.5:c.422A>T MANE Select	NP_808218.1:p.Asn141Ile