Canonical Allele Identifier: CA2578945851

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96122047_96122059del , CM000669.2:g.96122047_96122059del	GRCh38
NC_000007.13:g.95751359_95751371del , CM000669.1:g.95751359_95751371del	GRCh37
NC_000007.12:g.95589295_95589307del	NCBI36
NG_012247.1:g.205089_205101del
NG_012247.2:g.205089_205101del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1592-62_1592-50del MANE Select	ENSP00000265631.6:n.1592-62_1592-50del
ENST00000265631.9:c.1592-62_1592-50del	ENSP00000265631.5:n.1592-62_1592-50del
ENST00000416240.6:c.1595-62_1595-50del	ENSP00000400101.2:n.1595-62_1595-50del
NM_001160210.1:c.1595-62_1595-50del	NP_001153682.1:n.1595-62_1595-50del
NM_014251.2:c.1592-62_1592-50del	NP_055066.1:n.1592-62_1592-50del
NR_027662.1:n.1667-62_1667-50del
XM_006715831.2:c.1625-62_1625-50del	XP_006715894.1:n.1625-62_1625-50del
XM_011515728.1:c.740-62_740-50del	XP_011514030.1:n.740-62_740-50del
XM_006715831.4:c.1625-62_1625-50del	XP_006715894.1:n.1625-62_1625-50del
XM_017011663.1:c.1583-62_1583-50del	XP_016867152.1:n.1583-62_1583-50del
XM_017011664.2:c.740-62_740-50del	XP_016867153.1:n.740-62_740-50del
XM_017011665.1:c.740-62_740-50del	XP_016867154.1:n.740-62_740-50del
XR_001744525.2:n.1838-62_1838-50del
XR_002956405.1:n.2396-62_2396-50del
NM_014251.3:c.1592-62_1592-50del MANE Select	NP_055066.1:n.1592-62_1592-50del
NR_027662.2:n.1618-62_1618-50del
NM_001160210.2:c.1595-62_1595-50del	NP_001153682.1:n.1595-62_1595-50del