Canonical Allele Identifier: CA1727580560

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189552_96189559delinsCAAAAAAA , CM000669.2:g.96189552_96189559delinsCAAAAAAA	GRCh38
NC_000007.13:g.95818864_95818871delinsCAAAAAAA , CM000669.1:g.95818864_95818871delinsCAAAAAAA	GRCh37
NC_000007.12:g.95656800_95656807delinsCAAAAAAA	NCBI36
NG_012247.1:g.137589_137596delinsTTTTTTTG
NG_012247.2:g.137589_137596delinsTTTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+22_848+29delinsTTTTTTTG MANE Select	ENSP00000265631.6:n.848+22_848+29delinsTTTTTTTG
ENST00000265631.9:c.848+22_848+29delinsTTTTTTTG	ENSP00000265631.5:n.848+22_848+29delinsTTTTTTTG
ENST00000416240.6:c.848+22_848+29delinsTTTTTTTG	ENSP00000400101.2:n.848+22_848+29delinsTTTTTTTG
NM_001160210.1:c.848+22_848+29delinsTTTTTTTG	NP_001153682.1:n.848+22_848+29delinsTTTTTTTG
NM_014251.2:c.848+22_848+29delinsTTTTTTTG	NP_055066.1:n.848+22_848+29delinsTTTTTTTG
NR_027662.1:n.923+22_923+29delinsTTTTTTTG
XM_006715831.2:c.881+22_881+29delinsTTTTTTTG	XP_006715894.1:n.881+22_881+29delinsTTTTTTTG
XM_011515727.1:c.881+22_881+29delinsTTTTTTTG	XP_011514029.1:n.881+22_881+29delinsTTTTTTTG
XM_011515728.1:c.-4-181_-4-174delinsTTTTTTTG	XP_011514030.1:n.-4-181_-4-174delinsTTTTTTTG
XM_006715831.4:c.881+22_881+29delinsTTTTTTTG	XP_006715894.1:n.881+22_881+29delinsTTTTTTTG
XM_011515727.3:c.881+22_881+29delinsTTTTTTTG	XP_011514029.1:n.881+22_881+29delinsTTTTTTTG
XM_017011663.1:c.839+22_839+29delinsTTTTTTTG	XP_016867152.1:n.839+22_839+29delinsTTTTTTTG
XM_017011664.2:c.-4-181_-4-174delinsTTTTTTTG	XP_016867153.1:n.-4-181_-4-174delinsTTTTTTTG
XM_017011665.1:c.-4-181_-4-174delinsTTTTTTTG	XP_016867154.1:n.-4-181_-4-174delinsTTTTTTTG
XR_001744525.2:n.1019+22_1019+29delinsTTTTTTTG
XR_002956405.1:n.1161+22_1161+29delinsTTTTTTTG
NM_014251.3:c.848+22_848+29delinsTTTTTTTG MANE Select	NP_055066.1:n.848+22_848+29delinsTTTTTTTG
NR_027662.2:n.874+22_874+29delinsTTTTTTTG
NM_001160210.2:c.848+22_848+29delinsTTTTTTTG	NP_001153682.1:n.848+22_848+29delinsTTTTTTTG