Canonical Allele Identifier: CA368260064

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95813598G>T (hg19) ; chr7:g.96184286G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184286G>T , CM000669.2:g.96184286G>T	GRCh38
NC_000007.13:g.95813598G>T , CM000669.1:g.95813598G>T	GRCh37
NC_000007.12:g.95651534G>T	NCBI36
NG_012247.1:g.142862C>A
NG_012247.2:g.142862C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1168C>A MANE Select	ENSP00000265631.6:p.Leu390Met
ENST00000265631.9:c.1168C>A	ENSP00000265631.5:p.Leu390Met
ENST00000416240.6:c.1171C>A	ENSP00000400101.2:p.Leu391Met
ENST00000484495.5:n.321C>A
ENST00000490072.5:n.235C>A
ENST00000492869.1:n.289C>A
NM_001160210.1:c.1171C>A	NP_001153682.1:p.Leu391Met
NM_014251.2:c.1168C>A	NP_055066.1:p.Leu390Met
NR_027662.1:n.1243C>A
XM_006715831.2:c.1201C>A	XP_006715894.1:p.Leu401Met
XM_011515727.1:c.1201C>A	XP_011514029.1:p.Leu401Met
XM_011515728.1:c.316C>A	XP_011514030.1:p.Leu106Met
XM_006715831.4:c.1201C>A	XP_006715894.1:p.Leu401Met
XM_011515727.3:c.1201C>A	XP_011514029.1:p.Leu401Met
XM_017011663.1:c.1159C>A	XP_016867152.1:p.Leu387Met
XM_017011664.2:c.316C>A	XP_016867153.1:p.Leu106Met
XM_017011665.1:c.316C>A	XP_016867154.1:p.Leu106Met
XR_001744525.2:n.1339C>A
XR_002956405.1:n.1972C>A
NM_014251.3:c.1168C>A MANE Select	NP_055066.1:p.Leu390Met
NR_027662.2:n.1194C>A
NM_001160210.2:c.1171C>A	NP_001153682.1:p.Leu391Met