Canonical Allele Identifier: CA456510873

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818672G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189360G>A , CM000669.2:g.96189360G>A	GRCh38
NC_000007.13:g.95818672G>A , CM000669.1:g.95818672G>A	GRCh37
NC_000007.12:g.95656608G>A	NCBI36
NG_012247.1:g.137788C>T
NG_012247.2:g.137788C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.867C>T MANE Select	ENSP00000265631.6:p.Asp289=
ENST00000265631.9:c.867C>T	ENSP00000265631.5:p.Asp289=
ENST00000416240.6:c.867C>T	ENSP00000400101.2:p.Asp289=
ENST00000484495.5:n.20C>T
NM_001160210.1:c.867C>T	NP_001153682.1:p.Asp289=
NM_014251.2:c.867C>T	NP_055066.1:p.Asp289=
NR_027662.1:n.942C>T
XM_006715831.2:c.900C>T	XP_006715894.1:p.Asp300=
XM_011515727.1:c.900C>T	XP_011514029.1:p.Asp300=
XM_011515728.1:c.15C>T	XP_011514030.1:p.Asp5=
XM_006715831.4:c.900C>T	XP_006715894.1:p.Asp300=
XM_011515727.3:c.900C>T	XP_011514029.1:p.Asp300=
XM_017011663.1:c.858C>T	XP_016867152.1:p.Asp286=
XM_017011664.2:c.15C>T	XP_016867153.1:p.Asp5=
XM_017011665.1:c.15C>T	XP_016867154.1:p.Asp5=
XR_001744525.2:n.1038C>T
XR_002956405.1:n.1180C>T
NM_014251.3:c.867C>T MANE Select	NP_055066.1:p.Asp289=
NR_027662.2:n.893C>T
NM_001160210.2:c.867C>T	NP_001153682.1:p.Asp289=