Canonical Allele Identifier: CA368258660

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96121994-A-G
• MyVariant Identifiers: chr7:g.95751306A>G (hg19) ; chr7:g.96121994A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121994A>G , CM000669.2:g.96121994A>G	GRCh38
NC_000007.13:g.95751306A>G , CM000669.1:g.95751306A>G	GRCh37
NC_000007.12:g.95589242A>G	NCBI36
NG_012247.1:g.205154T>C
NG_012247.2:g.205154T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1595T>C MANE Select	ENSP00000265631.6:p.Met532Thr
ENST00000265631.9:c.1595T>C	ENSP00000265631.5:p.Met532Thr
ENST00000416240.6:c.1598T>C	ENSP00000400101.2:p.Met533Thr
ENST00000494085.1:n.5T>C
NM_001160210.1:c.1598T>C	NP_001153682.1:p.Met533Thr
NM_014251.2:c.1595T>C	NP_055066.1:p.Met532Thr
NR_027662.1:n.1670T>C
XM_006715831.2:c.1628T>C	XP_006715894.1:p.Met543Thr
XM_011515728.1:c.743T>C	XP_011514030.1:p.Met248Thr
XM_006715831.4:c.1628T>C	XP_006715894.1:p.Met543Thr
XM_017011663.1:c.1586T>C	XP_016867152.1:p.Met529Thr
XM_017011664.2:c.743T>C	XP_016867153.1:p.Met248Thr
XM_017011665.1:c.743T>C	XP_016867154.1:p.Met248Thr
XR_001744525.2:n.1841T>C
XR_002956405.1:n.2399T>C
NM_014251.3:c.1595T>C MANE Select	NP_055066.1:p.Met532Thr
NR_027662.2:n.1621T>C
NM_001160210.2:c.1598T>C	NP_001153682.1:p.Met533Thr