Canonical Allele Identifier: CA368263285

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95822360A>T (hg19) ; chr7:g.96193048A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193048A>T , CM000669.2:g.96193048A>T	GRCh38
NC_000007.13:g.95822360A>T , CM000669.1:g.95822360A>T	GRCh37
NC_000007.12:g.95660296A>T	NCBI36
NG_012247.1:g.134100T>A
NG_012247.2:g.134100T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.604T>A MANE Select	ENSP00000265631.6:p.Cys202Ser
ENST00000265631.9:c.604T>A	ENSP00000265631.5:p.Cys202Ser
ENST00000416240.6:c.604T>A	ENSP00000400101.2:p.Cys202Ser
NM_001160210.1:c.604T>A	NP_001153682.1:p.Cys202Ser
NM_014251.2:c.604T>A	NP_055066.1:p.Cys202Ser
NR_027662.1:n.679T>A
XM_006715831.2:c.637T>A	XP_006715894.1:p.Cys213Ser
XM_011515727.1:c.637T>A	XP_011514029.1:p.Cys213Ser
XM_006715831.4:c.637T>A	XP_006715894.1:p.Cys213Ser
XM_011515727.3:c.637T>A	XP_011514029.1:p.Cys213Ser
XM_017011663.1:c.595T>A	XP_016867152.1:p.Cys199Ser
XM_017011664.2:c.-155T>A	XP_016867153.1:n.-155T>A
XM_017011665.1:c.-155T>A	XP_016867154.1:n.-155T>A
XR_001744525.2:n.775T>A
XR_002956405.1:n.917T>A
NM_014251.3:c.604T>A MANE Select	NP_055066.1:p.Cys202Ser
NR_027662.2:n.630T>A
NM_001160210.2:c.604T>A	NP_001153682.1:p.Cys202Ser