Canonical Allele Identifier: CA1727518344

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121912G= , CM000669.2:g.96121912G=	GRCh38
NC_000007.13:g.95751224G= , CM000669.1:g.95751224G=	GRCh37
NC_000007.12:g.95589160G=	NCBI36
NG_012247.1:g.205236C=
NG_012247.2:g.205236C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1677C= MANE Select	ENSP00000265631.6:p.Tyr559=
ENST00000265631.9:c.1677C=	ENSP00000265631.5:p.Tyr559=
ENST00000416240.6:c.1680C=	ENSP00000400101.2:p.Tyr560=
ENST00000494085.1:n.87C=
NM_001160210.1:c.1680C=	NP_001153682.1:p.Tyr560=
NM_014251.2:c.1677C=	NP_055066.1:p.Tyr559=
NR_027662.1:n.1752C=
XM_006715831.2:c.1710C=	XP_006715894.1:p.Tyr570=
XM_011515728.1:c.825C=	XP_011514030.1:p.Tyr275=
XM_006715831.4:c.1710C=	XP_006715894.1:p.Tyr570=
XM_017011663.1:c.1668C=	XP_016867152.1:p.Tyr556=
XM_017011664.2:c.825C=	XP_016867153.1:p.Tyr275=
XM_017011665.1:c.825C=	XP_016867154.1:p.Tyr275=
XR_001744525.2:n.1923C=
XR_002956405.1:n.2481C=
NM_014251.3:c.1677C= MANE Select	NP_055066.1:p.Tyr559=
NR_027662.2:n.1703C=
NM_001160210.2:c.1680C=	NP_001153682.1:p.Tyr560=