Canonical Allele Identifier: CA2683825522

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96189551-C-CCAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189570_96189571insAAAAAAAAAAACAAAAAAAAAAAAAAAAAA , CM000669.2:g.96189570_96189571insAAAAAAAAAAACAAAAAAAAAAAAAAAAAA	GRCh38
NC_000007.13:g.95818882_95818883insAAAAAAAAAAACAAAAAAAAAAAAAAAAAA , CM000669.1:g.95818882_95818883insAAAAAAAAAAACAAAAAAAAAAAAAAAAAA	GRCh37
NC_000007.12:g.95656818_95656819insAAAAAAAAAAACAAAAAAAAAAAAAAAAAA	NCBI36
NG_012247.1:g.137596_137597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG
NG_012247.2:g.137596_137597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG MANE Select	ENSP00000265631.6:n.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000265631.9:c.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	ENSP00000265631.5:n.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTT...
ENST00000416240.6:c.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	ENSP00000400101.2:n.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001160210.1:c.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	NP_001153682.1:n.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_014251.2:c.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	NP_055066.1:n.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG
NR_027662.1:n.923+29_923+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG
XM_006715831.2:c.881+29_881+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	XP_006715894.1:n.881+29_881+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011515727.1:c.881+29_881+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	XP_011514029.1:n.881+29_881+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011515728.1:c.-4-174_-4-173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	XP_011514030.1:n.-4-174_-4-173insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_006715831.4:c.881+29_881+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	XP_006715894.1:n.881+29_881+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011515727.3:c.881+29_881+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	XP_011514029.1:n.881+29_881+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_017011663.1:c.839+29_839+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	XP_016867152.1:n.839+29_839+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_017011664.2:c.-4-174_-4-173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	XP_016867153.1:n.-4-174_-4-173insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_017011665.1:c.-4-174_-4-173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	XP_016867154.1:n.-4-174_-4-173insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XR_001744525.2:n.1019+29_1019+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG
XR_002956405.1:n.1161+29_1161+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG
NM_014251.3:c.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG MANE Select	NP_055066.1:n.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG
NR_027662.2:n.874+29_874+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG
NM_001160210.2:c.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	NP_001153682.1:n.848+29_848+30insTTTTTTTTTTTTTTTTTTTTTTTTTTTT...