Canonical Allele Identifier: CA1727574979
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96184282T= , CM000669.2:g.96184282T= GRCh38
NC_000007.13:g.95813594T= , CM000669.1:g.95813594T= GRCh37
NC_000007.12:g.95651530T= NCBI36
NG_012247.1:g.142866A=
NG_012247.2:g.142866A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265631.10:c.1172A= MANE Select ENSP00000265631.6:p.Tyr391=
ENST00000265631.9:c.1172A= ENSP00000265631.5:p.Tyr391=
ENST00000416240.6:c.1175A= ENSP00000400101.2:p.Tyr392=
ENST00000484495.5:n.325A=
ENST00000490072.5:n.239A=
ENST00000492869.1:n.293A=
NM_001160210.1:c.1175A= NP_001153682.1:p.Tyr392=
NM_014251.2:c.1172A= NP_055066.1:p.Tyr391=
NR_027662.1:n.1247A=
XM_006715831.2:c.1205A= XP_006715894.1:p.Tyr402=
XM_011515727.1:c.1205A= XP_011514029.1:p.Tyr402=
XM_011515728.1:c.320A= XP_011514030.1:p.Tyr107=
XM_006715831.4:c.1205A= XP_006715894.1:p.Tyr402=
XM_011515727.3:c.1205A= XP_011514029.1:p.Tyr402=
XM_017011663.1:c.1163A= XP_016867152.1:p.Tyr388=
XM_017011664.2:c.320A= XP_016867153.1:p.Tyr107=
XM_017011665.1:c.320A= XP_016867154.1:p.Tyr107=
XR_001744525.2:n.1343A=
XR_002956405.1:n.1976A=
NM_014251.3:c.1172A= MANE Select NP_055066.1:p.Tyr391=
NR_027662.2:n.1198A=
NM_001160210.2:c.1175A= NP_001153682.1:p.Tyr392=