Canonical Allele Identifier: CA368260053

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95813592T>A (hg19) ; chr7:g.96184280T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184280T>A , CM000669.2:g.96184280T>A	GRCh38
NC_000007.13:g.95813592T>A , CM000669.1:g.95813592T>A	GRCh37
NC_000007.12:g.95651528T>A	NCBI36
NG_012247.1:g.142868A>T
NG_012247.2:g.142868A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1174A>T MANE Select	ENSP00000265631.6:p.Arg392Ter
ENST00000265631.9:c.1174A>T	ENSP00000265631.5:p.Arg392Ter
ENST00000416240.6:c.1177A>T	ENSP00000400101.2:p.Arg393Ter
ENST00000484495.5:n.327A>T
ENST00000490072.5:n.241A>T
ENST00000492869.1:n.295A>T
NM_001160210.1:c.1177A>T	NP_001153682.1:p.Arg393Ter
NM_014251.2:c.1174A>T	NP_055066.1:p.Arg392Ter
NR_027662.1:n.1249A>T
XM_006715831.2:c.1207A>T	XP_006715894.1:p.Arg403Ter
XM_011515727.1:c.1207A>T	XP_011514029.1:p.Arg403Ter
XM_011515728.1:c.322A>T	XP_011514030.1:p.Arg108Ter
XM_006715831.4:c.1207A>T	XP_006715894.1:p.Arg403Ter
XM_011515727.3:c.1207A>T	XP_011514029.1:p.Arg403Ter
XM_017011663.1:c.1165A>T	XP_016867152.1:p.Arg389Ter
XM_017011664.2:c.322A>T	XP_016867153.1:p.Arg108Ter
XM_017011665.1:c.322A>T	XP_016867154.1:p.Arg108Ter
XR_001744525.2:n.1345A>T
XR_002956405.1:n.1978A>T
NM_014251.3:c.1174A>T MANE Select	NP_055066.1:p.Arg392Ter
NR_027662.2:n.1200A>T
NM_001160210.2:c.1177A>T	NP_001153682.1:p.Arg393Ter