Canonical Allele Identifier: CA368258255

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95751229T>G (hg19) ; chr7:g.96121917T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121917T>G , CM000669.2:g.96121917T>G	GRCh38
NC_000007.13:g.95751229T>G , CM000669.1:g.95751229T>G	GRCh37
NC_000007.12:g.95589165T>G	NCBI36
NG_012247.1:g.205231A>C
NG_012247.2:g.205231A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1672A>C MANE Select	ENSP00000265631.6:p.Thr558Pro
ENST00000265631.9:c.1672A>C	ENSP00000265631.5:p.Thr558Pro
ENST00000416240.6:c.1675A>C	ENSP00000400101.2:p.Thr559Pro
ENST00000494085.1:n.82A>C
NM_001160210.1:c.1675A>C	NP_001153682.1:p.Thr559Pro
NM_014251.2:c.1672A>C	NP_055066.1:p.Thr558Pro
NR_027662.1:n.1747A>C
XM_006715831.2:c.1705A>C	XP_006715894.1:p.Thr569Pro
XM_011515728.1:c.820A>C	XP_011514030.1:p.Thr274Pro
XM_006715831.4:c.1705A>C	XP_006715894.1:p.Thr569Pro
XM_017011663.1:c.1663A>C	XP_016867152.1:p.Thr555Pro
XM_017011664.2:c.820A>C	XP_016867153.1:p.Thr274Pro
XM_017011665.1:c.820A>C	XP_016867154.1:p.Thr274Pro
XR_001744525.2:n.1918A>C
XR_002956405.1:n.2476A>C
NM_014251.3:c.1672A>C MANE Select	NP_055066.1:p.Thr558Pro
NR_027662.2:n.1698A>C
NM_001160210.2:c.1675A>C	NP_001153682.1:p.Thr559Pro