Canonical Allele Identifier: CA368262266

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818661A>C (hg19) ; chr7:g.96189349A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189349A>C , CM000669.2:g.96189349A>C	GRCh38
NC_000007.13:g.95818661A>C , CM000669.1:g.95818661A>C	GRCh37
NC_000007.12:g.95656597A>C	NCBI36
NG_012247.1:g.137799T>G
NG_012247.2:g.137799T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.878T>G MANE Select	ENSP00000265631.6:p.Ile293Ser
ENST00000265631.9:c.878T>G	ENSP00000265631.5:p.Ile293Ser
ENST00000416240.6:c.878T>G	ENSP00000400101.2:p.Ile293Ser
ENST00000484495.5:n.31T>G
NM_001160210.1:c.878T>G	NP_001153682.1:p.Ile293Ser
NM_014251.2:c.878T>G	NP_055066.1:p.Ile293Ser
NR_027662.1:n.953T>G
XM_006715831.2:c.911T>G	XP_006715894.1:p.Ile304Ser
XM_011515727.1:c.911T>G	XP_011514029.1:p.Ile304Ser
XM_011515728.1:c.26T>G	XP_011514030.1:p.Ile9Ser
XM_006715831.4:c.911T>G	XP_006715894.1:p.Ile304Ser
XM_011515727.3:c.911T>G	XP_011514029.1:p.Ile304Ser
XM_017011663.1:c.869T>G	XP_016867152.1:p.Ile290Ser
XM_017011664.2:c.26T>G	XP_016867153.1:p.Ile9Ser
XM_017011665.1:c.26T>G	XP_016867154.1:p.Ile9Ser
XR_001744525.2:n.1049T>G
XR_002956405.1:n.1191T>G
NM_014251.3:c.878T>G MANE Select	NP_055066.1:p.Ile293Ser
NR_027662.2:n.904T>G
NM_001160210.2:c.878T>G	NP_001153682.1:p.Ile293Ser