Canonical Allele Identifier: CA368260056

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95813594T>A (hg19) ; chr7:g.96184282T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184282T>A , CM000669.2:g.96184282T>A	GRCh38
NC_000007.13:g.95813594T>A , CM000669.1:g.95813594T>A	GRCh37
NC_000007.12:g.95651530T>A	NCBI36
NG_012247.1:g.142866A>T
NG_012247.2:g.142866A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1172A>T MANE Select	ENSP00000265631.6:p.Tyr391Phe
ENST00000265631.9:c.1172A>T	ENSP00000265631.5:p.Tyr391Phe
ENST00000416240.6:c.1175A>T	ENSP00000400101.2:p.Tyr392Phe
ENST00000484495.5:n.325A>T
ENST00000490072.5:n.239A>T
ENST00000492869.1:n.293A>T
NM_001160210.1:c.1175A>T	NP_001153682.1:p.Tyr392Phe
NM_014251.2:c.1172A>T	NP_055066.1:p.Tyr391Phe
NR_027662.1:n.1247A>T
XM_006715831.2:c.1205A>T	XP_006715894.1:p.Tyr402Phe
XM_011515727.1:c.1205A>T	XP_011514029.1:p.Tyr402Phe
XM_011515728.1:c.320A>T	XP_011514030.1:p.Tyr107Phe
XM_006715831.4:c.1205A>T	XP_006715894.1:p.Tyr402Phe
XM_011515727.3:c.1205A>T	XP_011514029.1:p.Tyr402Phe
XM_017011663.1:c.1163A>T	XP_016867152.1:p.Tyr388Phe
XM_017011664.2:c.320A>T	XP_016867153.1:p.Tyr107Phe
XM_017011665.1:c.320A>T	XP_016867154.1:p.Tyr107Phe
XR_001744525.2:n.1343A>T
XR_002956405.1:n.1976A>T
NM_014251.3:c.1172A>T MANE Select	NP_055066.1:p.Tyr391Phe
NR_027662.2:n.1198A>T
NM_001160210.2:c.1175A>T	NP_001153682.1:p.Tyr392Phe