Canonical Allele Identifier: CA368263558

Gene: SLC25A13

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193177G>A , CM000669.2:g.96193177G>A	GRCh38
NC_000007.13:g.95822489G>A , CM000669.1:g.95822489G>A	GRCh37
NC_000007.12:g.95660425G>A	NCBI36
NG_012247.1:g.133971C>T
NG_012247.2:g.133971C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.475C>T MANE Select	ENSP00000265631.6:p.Gln159Ter
ENST00000265631.9:c.475C>T	ENSP00000265631.5:p.Gln159Ter
ENST00000416240.6:c.475C>T	ENSP00000400101.2:p.Gln159Ter
ENST00000472162.2:c.*137C>T	ENSP00000473505.1:n.*137C>T
NM_001160210.1:c.475C>T	NP_001153682.1:p.Gln159Ter
NM_014251.2:c.475C>T	NP_055066.1:p.Gln159Ter
NR_027662.1:n.550C>T
XM_006715831.2:c.508C>T	XP_006715894.1:p.Gln170Ter
XM_011515727.1:c.508C>T	XP_011514029.1:p.Gln170Ter
XM_006715831.4:c.508C>T	XP_006715894.1:p.Gln170Ter
XM_011515727.3:c.508C>T	XP_011514029.1:p.Gln170Ter
XM_017011663.1:c.466C>T	XP_016867152.1:p.Gln156Ter
XM_017011664.2:c.-284C>T	XP_016867153.1:n.-284C>T
XM_017011665.1:c.-284C>T	XP_016867154.1:n.-284C>T
XR_001744525.2:n.646C>T
XR_002956405.1:n.788C>T
NM_014251.3:c.475C>T MANE Select	NP_055066.1:p.Gln159Ter
NR_027662.2:n.501C>T
NM_001160210.2:c.475C>T	NP_001153682.1:p.Gln159Ter