Canonical Allele Identifier: CA368257370

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750627T>A (hg19) ; chr7:g.96121315T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121315T>A , CM000669.2:g.96121315T>A	GRCh38
NC_000007.13:g.95750627T>A , CM000669.1:g.95750627T>A	GRCh37
NC_000007.12:g.95588563T>A	NCBI36
NG_012247.1:g.205833A>T
NG_012247.2:g.205833A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1904A>T MANE Select	ENSP00000265631.6:p.Asp635Val
ENST00000265631.9:c.1904A>T	ENSP00000265631.5:p.Asp635Val
ENST00000416240.6:c.1907A>T	ENSP00000400101.2:p.Asp636Val
ENST00000494085.1:n.407A>T
NM_001160210.1:c.1907A>T	NP_001153682.1:p.Asp636Val
NM_014251.2:c.1904A>T	NP_055066.1:p.Asp635Val
NR_027662.1:n.1979A>T
XM_006715831.2:c.1937A>T	XP_006715894.1:p.Asp646Val
XM_011515728.1:c.1052A>T	XP_011514030.1:p.Asp351Val
XM_006715831.4:c.1937A>T	XP_006715894.1:p.Asp646Val
XM_017011663.1:c.1895A>T	XP_016867152.1:p.Asp632Val
XM_017011664.2:c.1052A>T	XP_016867153.1:p.Asp351Val
XM_017011665.1:c.1052A>T	XP_016867154.1:p.Asp351Val
XR_001744525.2:n.2150A>T
XR_002956405.1:n.2708A>T
NM_014251.3:c.1904A>T MANE Select	NP_055066.1:p.Asp635Val
NR_027662.2:n.1930A>T
NM_001160210.2:c.1907A>T	NP_001153682.1:p.Asp636Val