Canonical Allele Identifier: CA1727580524

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189543_96189546delinsAGCT , CM000669.2:g.96189543_96189546delinsAGCT	GRCh38
NC_000007.13:g.95818855_95818858delinsAGCT , CM000669.1:g.95818855_95818858delinsAGCT	GRCh37
NC_000007.12:g.95656791_95656794delinsAGCT	NCBI36
NG_012247.1:g.137602_137605delinsAGCT
NG_012247.2:g.137602_137605delinsAGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+35_848+38delinsAGCT MANE Select	ENSP00000265631.6:n.848+35_848+38delinsAGCT
ENST00000265631.9:c.848+35_848+38delinsAGCT	ENSP00000265631.5:n.848+35_848+38delinsAGCT
ENST00000416240.6:c.848+35_848+38delinsAGCT	ENSP00000400101.2:n.848+35_848+38delinsAGCT
NM_001160210.1:c.848+35_848+38delinsAGCT	NP_001153682.1:n.848+35_848+38delinsAGCT
NM_014251.2:c.848+35_848+38delinsAGCT	NP_055066.1:n.848+35_848+38delinsAGCT
NR_027662.1:n.923+35_923+38delinsAGCT
XM_006715831.2:c.881+35_881+38delinsAGCT	XP_006715894.1:n.881+35_881+38delinsAGCT
XM_011515727.1:c.881+35_881+38delinsAGCT	XP_011514029.1:n.881+35_881+38delinsAGCT
XM_011515728.1:c.-4-168_-4-165delinsAGCT	XP_011514030.1:n.-4-168_-4-165delinsAGCT
XM_006715831.4:c.881+35_881+38delinsAGCT	XP_006715894.1:n.881+35_881+38delinsAGCT
XM_011515727.3:c.881+35_881+38delinsAGCT	XP_011514029.1:n.881+35_881+38delinsAGCT
XM_017011663.1:c.839+35_839+38delinsAGCT	XP_016867152.1:n.839+35_839+38delinsAGCT
XM_017011664.2:c.-4-168_-4-165delinsAGCT	XP_016867153.1:n.-4-168_-4-165delinsAGCT
XM_017011665.1:c.-4-168_-4-165delinsAGCT	XP_016867154.1:n.-4-168_-4-165delinsAGCT
XR_001744525.2:n.1019+35_1019+38delinsAGCT
XR_002956405.1:n.1161+35_1161+38delinsAGCT
NM_014251.3:c.848+35_848+38delinsAGCT MANE Select	NP_055066.1:n.848+35_848+38delinsAGCT
NR_027662.2:n.874+35_874+38delinsAGCT
NM_001160210.2:c.848+35_848+38delinsAGCT	NP_001153682.1:n.848+35_848+38delinsAGCT