Canonical Allele Identifier: CA397744613

Gene: SLC13A5

Linked Data

• MyVariant Identifiers: chr17:g.6599184A>T (hg19) ; chr17:g.6695865A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695865A>T , CM000679.2:g.6695865A>T	GRCh38
NC_000017.10:g.6599184A>T , CM000679.1:g.6599184A>T	GRCh37
NC_000017.9:g.6539908A>T	NCBI36
NG_034220.1:g.22557T>A , LRG_1020:g.22557T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.916T>A MANE Select	ENSP00000406220.2:p.Tyr306Asn
ENST00000293800.10:c.865T>A	ENSP00000293800.6:p.Tyr289Asn
ENST00000381074.8:c.787T>A	ENSP00000370464.4:p.Tyr263Asn
ENST00000433363.6:c.916T>A	ENSP00000406220.2:p.Tyr306Asn
ENST00000572094.1:c.*666T>A	ENSP00000461495.1:n.*666T>A
ENST00000572727.1:n.25T>A
ENST00000573648.5:c.916T>A	ENSP00000459372.1:p.Tyr306Asn
ENST00000574824.5:n.2049T>A
NM_001143838.2:c.916T>A	NP_001137310.1:p.Tyr306Asn
NM_001284509.1:c.865T>A	NP_001271438.1:p.Tyr289Asn
NM_001284510.1:c.787T>A	NP_001271439.1:p.Tyr263Asn
NM_177550.4:c.916T>A , LRG_1020t1:c.916T>A	NP_808218.1:p.Tyr306Asn
XM_006721504.2:c.805T>A	XP_006721567.1:p.Tyr269Asn
XM_011523795.1:c.916T>A	XP_011522097.1:p.Tyr306Asn
XM_011523795.3:c.916T>A	XP_011522097.1:p.Tyr306Asn
NM_001143838.3:c.916T>A	NP_001137310.1:p.Tyr306Asn
NM_001284509.2:c.865T>A	NP_001271438.1:p.Tyr289Asn
NM_001284510.2:c.787T>A	NP_001271439.1:p.Tyr263Asn
NM_177550.5:c.916T>A MANE Select	NP_808218.1:p.Tyr306Asn