Canonical Allele Identifier: CA456632298

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1791526507
• MyVariant Identifiers: chr7:g.95751227A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121915A>G , CM000669.2:g.96121915A>G	GRCh38
NC_000007.13:g.95751227A>G , CM000669.1:g.95751227A>G	GRCh37
NC_000007.12:g.95589163A>G	NCBI36
NG_012247.1:g.205233T>C
NG_012247.2:g.205233T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1674T>C MANE Select	ENSP00000265631.6:p.Thr558=
ENST00000265631.9:c.1674T>C	ENSP00000265631.5:p.Thr558=
ENST00000416240.6:c.1677T>C	ENSP00000400101.2:p.Thr559=
ENST00000494085.1:n.84T>C
NM_001160210.1:c.1677T>C	NP_001153682.1:p.Thr559=
NM_014251.2:c.1674T>C	NP_055066.1:p.Thr558=
NR_027662.1:n.1749T>C
XM_006715831.2:c.1707T>C	XP_006715894.1:p.Thr569=
XM_011515728.1:c.822T>C	XP_011514030.1:p.Thr274=
XM_006715831.4:c.1707T>C	XP_006715894.1:p.Thr569=
XM_017011663.1:c.1665T>C	XP_016867152.1:p.Thr555=
XM_017011664.2:c.822T>C	XP_016867153.1:p.Thr274=
XM_017011665.1:c.822T>C	XP_016867154.1:p.Thr274=
XR_001744525.2:n.1920T>C
XR_002956405.1:n.2478T>C
NM_014251.3:c.1674T>C MANE Select	NP_055066.1:p.Thr558=
NR_027662.2:n.1700T>C
NM_001160210.2:c.1677T>C	NP_001153682.1:p.Thr559=