Canonical Allele Identifier: CA368262263

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818660A>C (hg19) ; chr7:g.96189348A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189348A>C , CM000669.2:g.96189348A>C	GRCh38
NC_000007.13:g.95818660A>C , CM000669.1:g.95818660A>C	GRCh37
NC_000007.12:g.95656596A>C	NCBI36
NG_012247.1:g.137800T>G
NG_012247.2:g.137800T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.879T>G MANE Select	ENSP00000265631.6:p.Ile293Met
ENST00000265631.9:c.879T>G	ENSP00000265631.5:p.Ile293Met
ENST00000416240.6:c.879T>G	ENSP00000400101.2:p.Ile293Met
ENST00000484495.5:n.32T>G
NM_001160210.1:c.879T>G	NP_001153682.1:p.Ile293Met
NM_014251.2:c.879T>G	NP_055066.1:p.Ile293Met
NR_027662.1:n.954T>G
XM_006715831.2:c.912T>G	XP_006715894.1:p.Ile304Met
XM_011515727.1:c.912T>G	XP_011514029.1:p.Ile304Met
XM_011515728.1:c.27T>G	XP_011514030.1:p.Ile9Met
XM_006715831.4:c.912T>G	XP_006715894.1:p.Ile304Met
XM_011515727.3:c.912T>G	XP_011514029.1:p.Ile304Met
XM_017011663.1:c.870T>G	XP_016867152.1:p.Ile290Met
XM_017011664.2:c.27T>G	XP_016867153.1:p.Ile9Met
XM_017011665.1:c.27T>G	XP_016867154.1:p.Ile9Met
XR_001744525.2:n.1050T>G
XR_002956405.1:n.1192T>G
NM_014251.3:c.879T>G MANE Select	NP_055066.1:p.Ile293Met
NR_027662.2:n.905T>G
NM_001160210.2:c.879T>G	NP_001153682.1:p.Ile293Met