Canonical Allele Identifier: CA368260086

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95813607A>T (hg19) ; chr7:g.96184295A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184295A>T , CM000669.2:g.96184295A>T	GRCh38
NC_000007.13:g.95813607A>T , CM000669.1:g.95813607A>T	GRCh37
NC_000007.12:g.95651543A>T	NCBI36
NG_012247.1:g.142853T>A
NG_012247.2:g.142853T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1159T>A MANE Select	ENSP00000265631.6:p.Phe387Ile
ENST00000265631.9:c.1159T>A	ENSP00000265631.5:p.Phe387Ile
ENST00000416240.6:c.1162T>A	ENSP00000400101.2:p.Phe388Ile
ENST00000484495.5:n.312T>A
ENST00000490072.5:n.226T>A
ENST00000492869.1:n.280T>A
NM_001160210.1:c.1162T>A	NP_001153682.1:p.Phe388Ile
NM_014251.2:c.1159T>A	NP_055066.1:p.Phe387Ile
NR_027662.1:n.1234T>A
XM_006715831.2:c.1192T>A	XP_006715894.1:p.Phe398Ile
XM_011515727.1:c.1192T>A	XP_011514029.1:p.Phe398Ile
XM_011515728.1:c.307T>A	XP_011514030.1:p.Phe103Ile
XM_006715831.4:c.1192T>A	XP_006715894.1:p.Phe398Ile
XM_011515727.3:c.1192T>A	XP_011514029.1:p.Phe398Ile
XM_017011663.1:c.1150T>A	XP_016867152.1:p.Phe384Ile
XM_017011664.2:c.307T>A	XP_016867153.1:p.Phe103Ile
XM_017011665.1:c.307T>A	XP_016867154.1:p.Phe103Ile
XR_001744525.2:n.1330T>A
XR_002956405.1:n.1963T>A
NM_014251.3:c.1159T>A MANE Select	NP_055066.1:p.Phe387Ile
NR_027662.2:n.1185T>A
NM_001160210.2:c.1162T>A	NP_001153682.1:p.Phe388Ile