Canonical Allele Identifier: CA1727518215

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121850T= , CM000669.2:g.96121850T=	GRCh38
NC_000007.13:g.95751162T= , CM000669.1:g.95751162T=	GRCh37
NC_000007.12:g.95589098T=	NCBI36
NG_012247.1:g.205298A=
NG_012247.2:g.205298A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1739A= MANE Select	ENSP00000265631.6:p.Lys580=
ENST00000265631.9:c.1739A=	ENSP00000265631.5:p.Lys580=
ENST00000416240.6:c.1742A=	ENSP00000400101.2:p.Lys581=
ENST00000494085.1:n.149A=
NM_001160210.1:c.1742A=	NP_001153682.1:p.Lys581=
NM_014251.2:c.1739A=	NP_055066.1:p.Lys580=
NR_027662.1:n.1814A=
XM_006715831.2:c.1772A=	XP_006715894.1:p.Lys591=
XM_011515728.1:c.887A=	XP_011514030.1:p.Lys296=
XM_006715831.4:c.1772A=	XP_006715894.1:p.Lys591=
XM_017011663.1:c.1730A=	XP_016867152.1:p.Lys577=
XM_017011664.2:c.887A=	XP_016867153.1:p.Lys296=
XM_017011665.1:c.887A=	XP_016867154.1:p.Lys296=
XR_001744525.2:n.1985A=
XR_002956405.1:n.2543A=
NM_014251.3:c.1739A= MANE Select	NP_055066.1:p.Lys580=
NR_027662.2:n.1765A=
NM_001160210.2:c.1742A=	NP_001153682.1:p.Lys581=