Canonical Allele Identifier: CA4352750

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121335G>A , CM000669.2:g.96121335G>A	GRCh38
NC_000007.13:g.95750647G>A , CM000669.1:g.95750647G>A	GRCh37
NC_000007.12:g.95588583G>A	NCBI36
NG_012247.1:g.205813C>T
NG_012247.2:g.205813C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1884C>T MANE Select	ENSP00000265631.6:p.Asn628=
ENST00000265631.9:c.1884C>T	ENSP00000265631.5:p.Asn628=
ENST00000416240.6:c.1887C>T	ENSP00000400101.2:p.Asn629=
ENST00000494085.1:n.387C>T
NM_001160210.1:c.1887C>T	NP_001153682.1:p.Asn629=
NM_014251.2:c.1884C>T	NP_055066.1:p.Asn628=
NR_027662.1:n.1959C>T
XM_006715831.2:c.1917C>T	XP_006715894.1:p.Asn639=
XM_011515728.1:c.1032C>T	XP_011514030.1:p.Asn344=
XM_006715831.4:c.1917C>T	XP_006715894.1:p.Asn639=
XM_017011663.1:c.1875C>T	XP_016867152.1:p.Asn625=
XM_017011664.2:c.1032C>T	XP_016867153.1:p.Asn344=
XM_017011665.1:c.1032C>T	XP_016867154.1:p.Asn344=
XR_001744525.2:n.2130C>T
XR_002956405.1:n.2688C>T
NM_014251.3:c.1884C>T MANE Select	NP_055066.1:p.Asn628=
NR_027662.2:n.1910C>T
NM_001160210.2:c.1887C>T	NP_001153682.1:p.Asn629=