Canonical Allele Identifier: CA163519725

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96277305T>C , CM000669.2:g.96277305T>C	GRCh38
NC_000007.13:g.95906617T>C , CM000669.1:g.95906617T>C	GRCh37
NC_000007.12:g.95744553T>C	NCBI36
NG_012247.1:g.49843A>G
NG_012247.2:g.49843A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014251.3:c.103A>G MANE Select	NP_055066.1:p.Met35Val
ENST00000265631.10:c.103A>G MANE Select	ENSP00000265631.6:p.Met35Val
NM_001160210.1:c.103A>G	NP_001153682.1:p.Met35Val
NM_001160210.2:c.103A>G	NP_001153682.1:p.Met35Val
NM_014251.2:c.103A>G	NP_055066.1:p.Met35Val
NR_027662.1:n.294A>G
NR_027662.2:n.245A>G
ENST00000265631.9:c.103A>G	ENSP00000265631.5:p.Met35Val
ENST00000416240.6:c.103A>G	ENSP00000400101.2:p.Met35Val
ENST00000472162.2:c.103A>G	ENSP00000473505.1:p.Met35Val
XM_006715831.2:c.136A>G	XP_006715894.1:p.Met46Val
XM_006715831.4:c.136A>G	XP_006715894.1:p.Met46Val
XM_011515727.1:c.136A>G	XP_011514029.1:p.Met46Val
XM_011515727.3:c.136A>G	XP_011514029.1:p.Met46Val
XM_017011663.1:c.94A>G	XP_016867152.1:p.Met32Val
XM_017011664.2:c.-656A>G	XP_016867153.1:n.-656A>G
XM_017011665.1:c.-540A>G	XP_016867154.1:n.-540A>G
XR_001744525.2:n.274A>G
XR_002956405.1:n.416A>G