Canonical Allele Identifier: CA2635728297

Gene: SLC13A5

Linked Data

• gnomAD v4: 17-6695952-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6695955del , CM000679.2:g.6695955del	GRCh38
NC_000017.10:g.6599274del , CM000679.1:g.6599274del	GRCh37
NC_000017.9:g.6539998del	NCBI36
NG_034220.1:g.22469del , LRG_1020:g.22469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.840-12del MANE Select	ENSP00000406220.2:n.840-12del
ENST00000293800.10:c.789-12del	ENSP00000293800.6:n.789-12del
ENST00000381074.8:c.711-12del	ENSP00000370464.4:n.711-12del
ENST00000433363.6:c.840-12del	ENSP00000406220.2:n.840-12del
ENST00000572094.1:c.*590-12del	ENSP00000461495.1:n.*590-12del
ENST00000573648.5:c.840-12del	ENSP00000459372.1:n.840-12del
ENST00000574824.5:n.1973-12del
NM_001143838.2:c.840-12del	NP_001137310.1:n.840-12del
NM_001284509.1:c.789-12del	NP_001271438.1:n.789-12del
NM_001284510.1:c.711-12del	NP_001271439.1:n.711-12del
NM_177550.4:c.840-12del , LRG_1020t1:c.840-12del	NP_808218.1:n.840-12del
XM_006721504.2:c.729-12del	XP_006721567.1:n.729-12del
XM_011523795.1:c.840-12del	XP_011522097.1:n.840-12del
XM_011523795.3:c.840-12del	XP_011522097.1:n.840-12del
NM_001143838.3:c.840-12del	NP_001137310.1:n.840-12del
NM_001284509.2:c.789-12del	NP_001271438.1:n.789-12del
NM_001284510.2:c.711-12del	NP_001271439.1:n.711-12del
NM_177550.5:c.840-12del MANE Select	NP_808218.1:n.840-12del