Canonical Allele Identifier: CA456510835

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818621A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189309A>C , CM000669.2:g.96189309A>C	GRCh38
NC_000007.13:g.95818621A>C , CM000669.1:g.95818621A>C	GRCh37
NC_000007.12:g.95656557A>C	NCBI36
NG_012247.1:g.137839T>G
NG_012247.2:g.137839T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.918T>G MANE Select	ENSP00000265631.6:p.Ala306=
ENST00000265631.9:c.918T>G	ENSP00000265631.5:p.Ala306=
ENST00000416240.6:c.918T>G	ENSP00000400101.2:p.Ala306=
ENST00000484495.5:n.71T>G
NM_001160210.1:c.918T>G	NP_001153682.1:p.Ala306=
NM_014251.2:c.918T>G	NP_055066.1:p.Ala306=
NR_027662.1:n.993T>G
XM_006715831.2:c.951T>G	XP_006715894.1:p.Ala317=
XM_011515727.1:c.951T>G	XP_011514029.1:p.Ala317=
XM_011515728.1:c.66T>G	XP_011514030.1:p.Ala22=
XM_006715831.4:c.951T>G	XP_006715894.1:p.Ala317=
XM_011515727.3:c.951T>G	XP_011514029.1:p.Ala317=
XM_017011663.1:c.909T>G	XP_016867152.1:p.Ala303=
XM_017011664.2:c.66T>G	XP_016867153.1:p.Ala22=
XM_017011665.1:c.66T>G	XP_016867154.1:p.Ala22=
XR_001744525.2:n.1089T>G
XR_002956405.1:n.1231T>G
NM_014251.3:c.918T>G MANE Select	NP_055066.1:p.Ala306=
NR_027662.2:n.944T>G
NM_001160210.2:c.918T>G	NP_001153682.1:p.Ala306=