Canonical Allele Identifier: CA2580774095

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193032C>A , CM000669.2:g.96193032C>A	GRCh38
NC_000007.13:g.95822344C>A , CM000669.1:g.95822344C>A	GRCh37
NC_000007.12:g.95660280C>A	NCBI36
NG_012247.1:g.134116G>T
NG_012247.2:g.134116G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.615+5G>T MANE Select	ENSP00000265631.6:n.615+5G>T
ENST00000265631.9:c.615+5G>T	ENSP00000265631.5:n.615+5G>T
ENST00000416240.6:c.615+5G>T	ENSP00000400101.2:n.615+5G>T
NM_001160210.1:c.615+5G>T	NP_001153682.1:n.615+5G>T
NM_014251.2:c.615+5G>T	NP_055066.1:n.615+5G>T
NR_027662.1:n.690+5G>T
XM_006715831.2:c.648+5G>T	XP_006715894.1:n.648+5G>T
XM_011515727.1:c.648+5G>T	XP_011514029.1:n.648+5G>T
XM_006715831.4:c.648+5G>T	XP_006715894.1:n.648+5G>T
XM_011515727.3:c.648+5G>T	XP_011514029.1:n.648+5G>T
XM_017011663.1:c.606+5G>T	XP_016867152.1:n.606+5G>T
XM_017011664.2:c.-144+5G>T	XP_016867153.1:n.-144+5G>T
XM_017011665.1:c.-144+5G>T	XP_016867154.1:n.-144+5G>T
XR_001744525.2:n.786+5G>T
XR_002956405.1:n.928+5G>T
NM_014251.3:c.615+5G>T MANE Select	NP_055066.1:n.615+5G>T
NR_027662.2:n.641+5G>T
NM_001160210.2:c.615+5G>T	NP_001153682.1:n.615+5G>T