Canonical Allele Identifier: CA368258266

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95751232T>C (hg19) ; chr7:g.96121920T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121920T>C , CM000669.2:g.96121920T>C	GRCh38
NC_000007.13:g.95751232T>C , CM000669.1:g.95751232T>C	GRCh37
NC_000007.12:g.95589168T>C	NCBI36
NG_012247.1:g.205228A>G
NG_012247.2:g.205228A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1669A>G MANE Select	ENSP00000265631.6:p.Thr557Ala
ENST00000265631.9:c.1669A>G	ENSP00000265631.5:p.Thr557Ala
ENST00000416240.6:c.1672A>G	ENSP00000400101.2:p.Thr558Ala
ENST00000494085.1:n.79A>G
NM_001160210.1:c.1672A>G	NP_001153682.1:p.Thr558Ala
NM_014251.2:c.1669A>G	NP_055066.1:p.Thr557Ala
NR_027662.1:n.1744A>G
XM_006715831.2:c.1702A>G	XP_006715894.1:p.Thr568Ala
XM_011515728.1:c.817A>G	XP_011514030.1:p.Thr273Ala
XM_006715831.4:c.1702A>G	XP_006715894.1:p.Thr568Ala
XM_017011663.1:c.1660A>G	XP_016867152.1:p.Thr554Ala
XM_017011664.2:c.817A>G	XP_016867153.1:p.Thr273Ala
XM_017011665.1:c.817A>G	XP_016867154.1:p.Thr273Ala
XR_001744525.2:n.1915A>G
XR_002956405.1:n.2473A>G
NM_014251.3:c.1669A>G MANE Select	NP_055066.1:p.Thr557Ala
NR_027662.2:n.1695A>G
NM_001160210.2:c.1672A>G	NP_001153682.1:p.Thr558Ala