Canonical Allele Identifier: CA1727517728

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121643_96121646delinsCATG , CM000669.2:g.96121643_96121646delinsCATG	GRCh38
NC_000007.13:g.95750955_95750958delinsCATG , CM000669.1:g.95750955_95750958delinsCATG	GRCh37
NC_000007.12:g.95588891_95588894delinsCATG	NCBI36
NG_012247.1:g.205502_205505delinsCATG
NG_012247.2:g.205502_205505delinsCATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1841+9_1841+12delinsCATG MANE Select	ENSP00000265631.6:n.1841+9_1841+12delinsCATG
ENST00000265631.9:c.1841+9_1841+12delinsCATG	ENSP00000265631.5:n.1841+9_1841+12delinsCATG
ENST00000416240.6:c.1844+9_1844+12delinsCATG	ENSP00000400101.2:n.1844+9_1844+12delinsCATG
ENST00000494085.1:n.344+9_344+12delinsCATG
NM_001160210.1:c.1844+9_1844+12delinsCATG	NP_001153682.1:n.1844+9_1844+12delinsCATG
NM_014251.2:c.1841+9_1841+12delinsCATG	NP_055066.1:n.1841+9_1841+12delinsCATG
NR_027662.1:n.1916+9_1916+12delinsCATG
XM_006715831.2:c.1874+9_1874+12delinsCATG	XP_006715894.1:n.1874+9_1874+12delinsCATG
XM_011515728.1:c.989+9_989+12delinsCATG	XP_011514030.1:n.989+9_989+12delinsCATG
XM_006715831.4:c.1874+9_1874+12delinsCATG	XP_006715894.1:n.1874+9_1874+12delinsCATG
XM_017011663.1:c.1832+9_1832+12delinsCATG	XP_016867152.1:n.1832+9_1832+12delinsCATG
XM_017011664.2:c.989+9_989+12delinsCATG	XP_016867153.1:n.989+9_989+12delinsCATG
XM_017011665.1:c.989+9_989+12delinsCATG	XP_016867154.1:n.989+9_989+12delinsCATG
XR_001744525.2:n.2087+9_2087+12delinsCATG
XR_002956405.1:n.2645+9_2645+12delinsCATG
NM_014251.3:c.1841+9_1841+12delinsCATG MANE Select	NP_055066.1:n.1841+9_1841+12delinsCATG
NR_027662.2:n.1867+9_1867+12delinsCATG
NM_001160210.2:c.1844+9_1844+12delinsCATG	NP_001153682.1:n.1844+9_1844+12delinsCATG