Canonical Allele Identifier: CA1727580004

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189095_96189096delinsCA , CM000669.2:g.96189095_96189096delinsCA	GRCh38
NC_000007.13:g.95818407_95818408delinsCA , CM000669.1:g.95818407_95818408delinsCA	GRCh37
NC_000007.12:g.95656343_95656344delinsCA	NCBI36
NG_012247.1:g.138052_138053delinsTG
NG_012247.2:g.138052_138053delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.933+198_933+199delinsTG MANE Select	ENSP00000265631.6:n.933+198_933+199delinsTG
ENST00000265631.9:c.933+198_933+199delinsTG	ENSP00000265631.5:n.933+198_933+199delinsTG
ENST00000416240.6:c.933+198_933+199delinsTG	ENSP00000400101.2:n.933+198_933+199delinsTG
ENST00000484495.5:n.86+198_86+199delinsTG
NM_001160210.1:c.933+198_933+199delinsTG	NP_001153682.1:n.933+198_933+199delinsTG
NM_014251.2:c.933+198_933+199delinsTG	NP_055066.1:n.933+198_933+199delinsTG
NR_027662.1:n.1008+198_1008+199delinsTG
XM_006715831.2:c.966+198_966+199delinsTG	XP_006715894.1:n.966+198_966+199delinsTG
XM_011515727.1:c.966+198_966+199delinsTG	XP_011514029.1:n.966+198_966+199delinsTG
XM_011515728.1:c.81+198_81+199delinsTG	XP_011514030.1:n.81+198_81+199delinsTG
XM_006715831.4:c.966+198_966+199delinsTG	XP_006715894.1:n.966+198_966+199delinsTG
XM_011515727.3:c.966+198_966+199delinsTG	XP_011514029.1:n.966+198_966+199delinsTG
XM_017011663.1:c.924+198_924+199delinsTG	XP_016867152.1:n.924+198_924+199delinsTG
XM_017011664.2:c.81+198_81+199delinsTG	XP_016867153.1:n.81+198_81+199delinsTG
XM_017011665.1:c.81+198_81+199delinsTG	XP_016867154.1:n.81+198_81+199delinsTG
XR_001744525.2:n.1104+198_1104+199delinsTG
XR_002956405.1:n.1246+198_1246+199delinsTG
NM_014251.3:c.933+198_933+199delinsTG MANE Select	NP_055066.1:n.933+198_933+199delinsTG
NR_027662.2:n.959+198_959+199delinsTG
NM_001160210.2:c.933+198_933+199delinsTG	NP_001153682.1:n.933+198_933+199delinsTG