Canonical Allele Identifier: CA4352694

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121000A>G , CM000669.2:g.96121000A>G	GRCh38
NC_000007.13:g.95750312A>G , CM000669.1:g.95750312A>G	GRCh37
NC_000007.12:g.95588248A>G	NCBI36
NG_012247.1:g.206148T>C
NG_012247.2:g.206148T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.*191T>C MANE Select	ENSP00000265631.6:n.*191T>C
ENST00000265631.9:c.*191T>C	ENSP00000265631.5:n.*191T>C
ENST00000416240.6:c.*191T>C	ENSP00000400101.2:n.*191T>C
ENST00000494085.1:n.722T>C
NM_001160210.1:c.*191T>C	NP_001153682.1:n.*191T>C
NM_014251.2:c.*191T>C	NP_055066.1:n.*191T>C
NR_027662.1:n.2294T>C
XM_006715831.2:c.*191T>C	XP_006715894.1:n.*191T>C
XM_011515728.1:c.*191T>C	XP_011514030.1:n.*191T>C
XM_006715831.4:c.*191T>C	XP_006715894.1:n.*191T>C
XM_017011663.1:c.*191T>C	XP_016867152.1:n.*191T>C
XM_017011664.2:c.*191T>C	XP_016867153.1:n.*191T>C
XM_017011665.1:c.*191T>C	XP_016867154.1:n.*191T>C
XR_001744525.2:n.2465T>C
XR_002956405.1:n.3023T>C
NM_014251.3:c.*191T>C MANE Select	NP_055066.1:n.*191T>C
NR_027662.2:n.2245T>C
NM_001160210.2:c.*191T>C	NP_001153682.1:n.*191T>C