Canonical Allele Identifier: CA1104707399

Gene: SLC25A13

Linked Data

• gnomAD v3: 7-96189552-C-CAAAAAAAAAAAAAAAAAAAAAAAAAAA
• gnomAD v4: 7-96189552-C-CAAAAAAAAAAAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189570_96189571insAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000669.2:g.96189570_96189571insAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000007.13:g.95818882_95818883insAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000669.1:g.95818882_95818883insAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000007.12:g.95656818_95656819insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_012247.1:g.137595_137596insTTTTTTTTTTTTTTTTTTTTTTTTTTT
NG_012247.2:g.137595_137596insTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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