Canonical Allele Identifier: CA368263122

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96191189G>C , CM000669.2:g.96191189G>C	GRCh38
NC_000007.13:g.95820501G>C , CM000669.1:g.95820501G>C	GRCh37
NC_000007.12:g.95658437G>C	NCBI36
NG_012247.1:g.135959C>G
NG_012247.2:g.135959C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.674C>G MANE Select	ENSP00000265631.6:p.Ser225Trp
ENST00000265631.9:c.674C>G	ENSP00000265631.5:p.Ser225Trp
ENST00000416240.6:c.674C>G	ENSP00000400101.2:p.Ser225Trp
NM_001160210.1:c.674C>G	NP_001153682.1:p.Ser225Trp
NM_014251.2:c.674C>G	NP_055066.1:p.Ser225Trp
NR_027662.1:n.749C>G
XM_006715831.2:c.707C>G	XP_006715894.1:p.Ser236Trp
XM_011515727.1:c.707C>G	XP_011514029.1:p.Ser236Trp
XM_011515728.1:c.-85C>G	XP_011514030.1:n.-85C>G
XM_006715831.4:c.707C>G	XP_006715894.1:p.Ser236Trp
XM_011515727.3:c.707C>G	XP_011514029.1:p.Ser236Trp
XM_017011663.1:c.665C>G	XP_016867152.1:p.Ser222Trp
XM_017011664.2:c.-85C>G	XP_016867153.1:n.-85C>G
XM_017011665.1:c.-85C>G	XP_016867154.1:n.-85C>G
XR_001744525.2:n.845C>G
XR_002956405.1:n.987C>G
NM_014251.3:c.674C>G MANE Select	NP_055066.1:p.Ser225Trp
NR_027662.2:n.700C>G
NM_001160210.2:c.674C>G	NP_001153682.1:p.Ser225Trp