Canonical Allele Identifier: CA1104707268

Gene: SLC25A13

Linked Data

• gnomAD v3: 7-96189541-T-TTAAAAAAAAAAA
• gnomAD v4: 7-96189541-T-TTAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189541_96189542insTAAAAAAAAAAA , CM000669.2:g.96189541_96189542insTAAAAAAAAAAA	GRCh38
NC_000007.13:g.95818853_95818854insTAAAAAAAAAAA , CM000669.1:g.95818853_95818854insTAAAAAAAAAAA	GRCh37
NC_000007.12:g.95656789_95656790insTAAAAAAAAAAA	NCBI36
NG_012247.1:g.137606_137607insTTTTTTTTTTTA
NG_012247.2:g.137606_137607insTTTTTTTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+39_848+40insTTTTTTTTTTTA MANE Select	ENSP00000265631.6:n.848+39_848+40insTTTTTTTTTTTA
ENST00000265631.9:c.848+39_848+40insTTTTTTTTTTTA	ENSP00000265631.5:n.848+39_848+40insTTTTTTTTTTTA
ENST00000416240.6:c.848+39_848+40insTTTTTTTTTTTA	ENSP00000400101.2:n.848+39_848+40insTTTTTTTTTTTA
NM_001160210.1:c.848+39_848+40insTTTTTTTTTTTA	NP_001153682.1:n.848+39_848+40insTTTTTTTTTTTA
NM_014251.2:c.848+39_848+40insTTTTTTTTTTTA	NP_055066.1:n.848+39_848+40insTTTTTTTTTTTA
NR_027662.1:n.923+39_923+40insTTTTTTTTTTTA
XM_006715831.2:c.881+39_881+40insTTTTTTTTTTTA	XP_006715894.1:n.881+39_881+40insTTTTTTTTTTTA
XM_011515727.1:c.881+39_881+40insTTTTTTTTTTTA	XP_011514029.1:n.881+39_881+40insTTTTTTTTTTTA
XM_011515728.1:c.-4-164_-4-163insTTTTTTTTTTTA	XP_011514030.1:n.-4-164_-4-163insTTTTTTTTTTTA
XM_006715831.4:c.881+39_881+40insTTTTTTTTTTTA	XP_006715894.1:n.881+39_881+40insTTTTTTTTTTTA
XM_011515727.3:c.881+39_881+40insTTTTTTTTTTTA	XP_011514029.1:n.881+39_881+40insTTTTTTTTTTTA
XM_017011663.1:c.839+39_839+40insTTTTTTTTTTTA	XP_016867152.1:n.839+39_839+40insTTTTTTTTTTTA
XM_017011664.2:c.-4-164_-4-163insTTTTTTTTTTTA	XP_016867153.1:n.-4-164_-4-163insTTTTTTTTTTTA
XM_017011665.1:c.-4-164_-4-163insTTTTTTTTTTTA	XP_016867154.1:n.-4-164_-4-163insTTTTTTTTTTTA
XR_001744525.2:n.1019+39_1019+40insTTTTTTTTTTTA
XR_002956405.1:n.1161+39_1161+40insTTTTTTTTTTTA
NM_014251.3:c.848+39_848+40insTTTTTTTTTTTA MANE Select	NP_055066.1:n.848+39_848+40insTTTTTTTTTTTA
NR_027662.2:n.874+39_874+40insTTTTTTTTTTTA
NM_001160210.2:c.848+39_848+40insTTTTTTTTTTTA	NP_001153682.1:n.848+39_848+40insTTTTTTTTTTTA