Canonical Allele Identifier: CA2777032098

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189570_96189571insAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000669.2:g.96189570_96189571insAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000007.13:g.95818882_95818883insAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000669.1:g.95818882_95818883insAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000007.12:g.95656818_95656819insAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_012247.1:g.137595_137596insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT
NG_012247.2:g.137595_137596insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000265631.6:n.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTT...
ENST00000265631.9:c.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000265631.5:n.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTT...
ENST00000416240.6:c.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000400101.2:n.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTT...
NM_001160210.1:c.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	NP_001153682.1:n.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTT...
NM_014251.2:c.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	NP_055066.1:n.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTT...
NR_027662.1:n.923+28_923+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT
XM_006715831.2:c.881+28_881+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	XP_006715894.1:n.881+28_881+29insTTTTTTTTTTATTTTTTTTTTTTTTTTT...
XM_011515727.1:c.881+28_881+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	XP_011514029.1:n.881+28_881+29insTTTTTTTTTTATTTTTTTTTTTTTTTTT...
XM_011515728.1:c.-4-175_-4-174insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	XP_011514030.1:n.-4-175_-4-174insTTTTTTTTTTATTTTTTTTTTTTTTTTT...
XM_006715831.4:c.881+28_881+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	XP_006715894.1:n.881+28_881+29insTTTTTTTTTTATTTTTTTTTTTTTTTTT...
XM_011515727.3:c.881+28_881+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	XP_011514029.1:n.881+28_881+29insTTTTTTTTTTATTTTTTTTTTTTTTTTT...
XM_017011663.1:c.839+28_839+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	XP_016867152.1:n.839+28_839+29insTTTTTTTTTTATTTTTTTTTTTTTTTTT...
XM_017011664.2:c.-4-175_-4-174insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	XP_016867153.1:n.-4-175_-4-174insTTTTTTTTTTATTTTTTTTTTTTTTTTT...
XM_017011665.1:c.-4-175_-4-174insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	XP_016867154.1:n.-4-175_-4-174insTTTTTTTTTTATTTTTTTTTTTTTTTTT...
XR_001744525.2:n.1019+28_1019+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT
XR_002956405.1:n.1161+28_1161+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT
NM_014251.3:c.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_055066.1:n.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTT...
NR_027662.2:n.874+28_874+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT
NM_001160210.2:c.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT	NP_001153682.1:n.848+28_848+29insTTTTTTTTTTATTTTTTTTTTTTTTTTT...