Canonical Allele Identifier: CA368257174
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96121262T>A , CM000669.2:g.96121262T>A GRCh38
NC_000007.13:g.95750574T>A , CM000669.1:g.95750574T>A GRCh37
NC_000007.12:g.95588510T>A NCBI36
NG_012247.1:g.205886A>T
NG_012247.2:g.205886A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.1957A>T MANE Select ENSP00000265631.6:p.Lys653Ter
ENST00000265631.9:c.1957A>T ENSP00000265631.5:p.Lys653Ter
ENST00000416240.6:c.1960A>T ENSP00000400101.2:p.Lys654Ter
ENST00000494085.1:n.460A>T
NM_001160210.1:c.1960A>T NP_001153682.1:p.Lys654Ter
NM_014251.2:c.1957A>T NP_055066.1:p.Lys653Ter
NR_027662.1:n.2032A>T
XM_006715831.2:c.1990A>T XP_006715894.1:p.Lys664Ter
XM_011515728.1:c.1105A>T XP_011514030.1:p.Lys369Ter
XM_006715831.4:c.1990A>T XP_006715894.1:p.Lys664Ter
XM_017011663.1:c.1948A>T XP_016867152.1:p.Lys650Ter
XM_017011664.2:c.1105A>T XP_016867153.1:p.Lys369Ter
XM_017011665.1:c.1105A>T XP_016867154.1:p.Lys369Ter
XR_001744525.2:n.2203A>T
XR_002956405.1:n.2761A>T
NM_014251.3:c.1957A>T MANE Select NP_055066.1:p.Lys653Ter
NR_027662.2:n.1983A>T
NM_001160210.2:c.1960A>T NP_001153682.1:p.Lys654Ter