Canonical Allele Identifier: CA368263341

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95822385A>C (hg19) ; chr7:g.96193073A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193073A>C , CM000669.2:g.96193073A>C	GRCh38
NC_000007.13:g.95822385A>C , CM000669.1:g.95822385A>C	GRCh37
NC_000007.12:g.95660321A>C	NCBI36
NG_012247.1:g.134075T>G
NG_012247.2:g.134075T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.579T>G MANE Select	ENSP00000265631.6:p.His193Gln
ENST00000265631.9:c.579T>G	ENSP00000265631.5:p.His193Gln
ENST00000416240.6:c.579T>G	ENSP00000400101.2:p.His193Gln
NM_001160210.1:c.579T>G	NP_001153682.1:p.His193Gln
NM_014251.2:c.579T>G	NP_055066.1:p.His193Gln
NR_027662.1:n.654T>G
XM_006715831.2:c.612T>G	XP_006715894.1:p.His204Gln
XM_011515727.1:c.612T>G	XP_011514029.1:p.His204Gln
XM_006715831.4:c.612T>G	XP_006715894.1:p.His204Gln
XM_011515727.3:c.612T>G	XP_011514029.1:p.His204Gln
XM_017011663.1:c.570T>G	XP_016867152.1:p.His190Gln
XM_017011664.2:c.-180T>G	XP_016867153.1:n.-180T>G
XM_017011665.1:c.-180T>G	XP_016867154.1:n.-180T>G
XR_001744525.2:n.750T>G
XR_002956405.1:n.892T>G
NM_014251.3:c.579T>G MANE Select	NP_055066.1:p.His193Gln
NR_027662.2:n.605T>G
NM_001160210.2:c.579T>G	NP_001153682.1:p.His193Gln