Canonical Allele Identifier: CA456510237

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95813605G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184293G>A , CM000669.2:g.96184293G>A	GRCh38
NC_000007.13:g.95813605G>A , CM000669.1:g.95813605G>A	GRCh37
NC_000007.12:g.95651541G>A	NCBI36
NG_012247.1:g.142855C>T
NG_012247.2:g.142855C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1161C>T MANE Select	ENSP00000265631.6:p.Phe387=
ENST00000265631.9:c.1161C>T	ENSP00000265631.5:p.Phe387=
ENST00000416240.6:c.1164C>T	ENSP00000400101.2:p.Phe388=
ENST00000484495.5:n.314C>T
ENST00000490072.5:n.228C>T
ENST00000492869.1:n.282C>T
NM_001160210.1:c.1164C>T	NP_001153682.1:p.Phe388=
NM_014251.2:c.1161C>T	NP_055066.1:p.Phe387=
NR_027662.1:n.1236C>T
XM_006715831.2:c.1194C>T	XP_006715894.1:p.Phe398=
XM_011515727.1:c.1194C>T	XP_011514029.1:p.Phe398=
XM_011515728.1:c.309C>T	XP_011514030.1:p.Phe103=
XM_006715831.4:c.1194C>T	XP_006715894.1:p.Phe398=
XM_011515727.3:c.1194C>T	XP_011514029.1:p.Phe398=
XM_017011663.1:c.1152C>T	XP_016867152.1:p.Phe384=
XM_017011664.2:c.309C>T	XP_016867153.1:p.Phe103=
XM_017011665.1:c.309C>T	XP_016867154.1:p.Phe103=
XR_001744525.2:n.1332C>T
XR_002956405.1:n.1965C>T
NM_014251.3:c.1161C>T MANE Select	NP_055066.1:p.Phe387=
NR_027662.2:n.1187C>T
NM_001160210.2:c.1164C>T	NP_001153682.1:p.Phe388=