Canonical Allele Identifier: CA1727517420

Gene: SLC25A13

Linked Data

• dbSNP Id: rs766856931

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121416dup , CM000669.2:g.96121416dup	GRCh38
NC_000007.13:g.95750728dup , CM000669.1:g.95750728dup	GRCh37
NC_000007.12:g.95588664dup	NCBI36
NG_012247.1:g.205737dup
NG_012247.2:g.205737dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1842-34dup MANE Select	ENSP00000265631.6:n.1842-34dup
ENST00000265631.9:c.1842-34dup	ENSP00000265631.5:n.1842-34dup
ENST00000416240.6:c.1845-34dup	ENSP00000400101.2:n.1845-34dup
ENST00000494085.1:n.345-34dup
NM_001160210.1:c.1845-34dup	NP_001153682.1:n.1845-34dup
NM_014251.2:c.1842-34dup	NP_055066.1:n.1842-34dup
NR_027662.1:n.1917-34dup
XM_006715831.2:c.1875-34dup	XP_006715894.1:n.1875-34dup
XM_011515728.1:c.990-34dup	XP_011514030.1:n.990-34dup
XM_006715831.4:c.1875-34dup	XP_006715894.1:n.1875-34dup
XM_017011663.1:c.1833-34dup	XP_016867152.1:n.1833-34dup
XM_017011664.2:c.990-34dup	XP_016867153.1:n.990-34dup
XM_017011665.1:c.990-34dup	XP_016867154.1:n.990-34dup
XR_001744525.2:n.2088-34dup
XR_002956405.1:n.2646-34dup
NM_014251.3:c.1842-34dup MANE Select	NP_055066.1:n.1842-34dup
NR_027662.2:n.1868-34dup
NM_001160210.2:c.1845-34dup	NP_001153682.1:n.1845-34dup