Canonical Allele Identifier: CA2566489457

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121761_96121763del , CM000669.2:g.96121761_96121763del	GRCh38
NC_000007.13:g.95751073_95751075del , CM000669.1:g.95751073_95751075del	GRCh37
NC_000007.12:g.95589009_95589011del	NCBI36
NG_012247.1:g.205386_205388del
NG_012247.2:g.205386_205388del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1751-17_1751-15del MANE Select	ENSP00000265631.6:n.1751-17_1751-15del
ENST00000265631.9:c.1751-17_1751-15del	ENSP00000265631.5:n.1751-17_1751-15del
ENST00000416240.6:c.1754-17_1754-15del	ENSP00000400101.2:n.1754-17_1754-15del
ENST00000494085.1:n.237_239del
NM_001160210.1:c.1754-17_1754-15del	NP_001153682.1:n.1754-17_1754-15del
NM_014251.2:c.1751-17_1751-15del	NP_055066.1:n.1751-17_1751-15del
NR_027662.1:n.1826-17_1826-15del
XM_006715831.2:c.1784-17_1784-15del	XP_006715894.1:n.1784-17_1784-15del
XM_011515728.1:c.899-17_899-15del	XP_011514030.1:n.899-17_899-15del
XM_006715831.4:c.1784-17_1784-15del	XP_006715894.1:n.1784-17_1784-15del
XM_017011663.1:c.1742-17_1742-15del	XP_016867152.1:n.1742-17_1742-15del
XM_017011664.2:c.899-17_899-15del	XP_016867153.1:n.899-17_899-15del
XM_017011665.1:c.899-17_899-15del	XP_016867154.1:n.899-17_899-15del
XR_001744525.2:n.1997-17_1997-15del
XR_002956405.1:n.2555-17_2555-15del
NM_014251.3:c.1751-17_1751-15del MANE Select	NP_055066.1:n.1751-17_1751-15del
NR_027662.2:n.1777-17_1777-15del
NM_001160210.2:c.1754-17_1754-15del	NP_001153682.1:n.1754-17_1754-15del