Canonical Allele Identifier: CA2777032059

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189544_96189545insAAA , CM000669.2:g.96189544_96189545insAAA	GRCh38
NC_000007.13:g.95818856_95818857insAAA , CM000669.1:g.95818856_95818857insAAA	GRCh37
NC_000007.12:g.95656792_95656793insAAA	NCBI36
NG_012247.1:g.137603_137604insTTT
NG_012247.2:g.137603_137604insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+36_848+37insTTT MANE Select	ENSP00000265631.6:n.848+36_848+37insTTT
ENST00000265631.9:c.848+36_848+37insTTT	ENSP00000265631.5:n.848+36_848+37insTTT
ENST00000416240.6:c.848+36_848+37insTTT	ENSP00000400101.2:n.848+36_848+37insTTT
NM_001160210.1:c.848+36_848+37insTTT	NP_001153682.1:n.848+36_848+37insTTT
NM_014251.2:c.848+36_848+37insTTT	NP_055066.1:n.848+36_848+37insTTT
NR_027662.1:n.923+36_923+37insTTT
XM_006715831.2:c.881+36_881+37insTTT	XP_006715894.1:n.881+36_881+37insTTT
XM_011515727.1:c.881+36_881+37insTTT	XP_011514029.1:n.881+36_881+37insTTT
XM_011515728.1:c.-4-167_-4-166insTTT	XP_011514030.1:n.-4-167_-4-166insTTT
XM_006715831.4:c.881+36_881+37insTTT	XP_006715894.1:n.881+36_881+37insTTT
XM_011515727.3:c.881+36_881+37insTTT	XP_011514029.1:n.881+36_881+37insTTT
XM_017011663.1:c.839+36_839+37insTTT	XP_016867152.1:n.839+36_839+37insTTT
XM_017011664.2:c.-4-167_-4-166insTTT	XP_016867153.1:n.-4-167_-4-166insTTT
XM_017011665.1:c.-4-167_-4-166insTTT	XP_016867154.1:n.-4-167_-4-166insTTT
XR_001744525.2:n.1019+36_1019+37insTTT
XR_002956405.1:n.1161+36_1161+37insTTT
NM_014251.3:c.848+36_848+37insTTT MANE Select	NP_055066.1:n.848+36_848+37insTTT
NR_027662.2:n.874+36_874+37insTTT
NM_001160210.2:c.848+36_848+37insTTT	NP_001153682.1:n.848+36_848+37insTTT