Canonical Allele Identifier: CA287381079

Gene: SLC13A5 C17orf100 ALOX15P1

Linked Data

• dbSNP Id: rs886603044
• gnomAD v2: 17-6590670-T-C
• gnomAD v3: 17-6687351-T-C
• gnomAD v4: 17-6687351-T-C
• MyVariant Identifiers: chr17:g.6590670T>C (hg19) ; chr17:g.6687351T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6687351T>C , CM000679.2:g.6687351T>C	GRCh38
NC_000017.10:g.6590670T>C , CM000679.1:g.6590670T>C	GRCh37
NC_000017.9:g.6531394T>C	NCBI36
NG_034220.1:g.31071A>G , LRG_1020:g.31071A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433363.7:c.1575+178A>G (SLC13A5) MANE Select	ENSP00000406220.2:n.1575+178A>G
ENST00000635042.1:n.725-5514T>C (C17orf100)
ENST00000293800.10:c.1524+178A>G (SLC13A5)	ENSP00000293800.6:n.1524+178A>G
ENST00000381074.8:c.1446+178A>G (SLC13A5)	ENSP00000370464.4:n.1446+178A>G
ENST00000433363.6:c.1575+178A>G (SLC13A5)	ENSP00000406220.2:n.1575+178A>G
ENST00000573648.5:c.1438-1013A>G (SLC13A5)	ENSP00000459372.1:n.1438-1013A>G
ENST00000574580.2:n.2770A>G (SLC13A5)
ENST00000634558.1:n.511-2525T>C (ALOX15P1)
ENST00000634823.1:n.265-5514T>C (ALOX15P1)
NM_001143838.2:c.1438-1013A>G (SLC13A5)	NP_001137310.1:n.1438-1013A>G
NM_001284509.1:c.1524+178A>G (SLC13A5)	NP_001271438.1:n.1524+178A>G
NM_001284510.1:c.1446+178A>G (SLC13A5)	NP_001271439.1:n.1446+178A>G
NM_177550.4:c.1575+178A>G , LRG_1020t1:c.1575+178A>G (SLC13A5)	NP_808218.1:n.1575+178A>G
XM_006721504.2:c.1464+178A>G (SLC13A5)	XP_006721567.1:n.1464+178A>G
NM_001143838.3:c.1438-1013A>G (SLC13A5)	NP_001137310.1:n.1438-1013A>G
NM_001284509.2:c.1524+178A>G (SLC13A5)	NP_001271438.1:n.1524+178A>G
NM_001284510.2:c.1446+178A>G (SLC13A5)	NP_001271439.1:n.1446+178A>G
NM_177550.5:c.1575+178A>G (SLC13A5) MANE Select	NP_808218.1:n.1575+178A>G