Canonical Allele Identifier: CA1727518276

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121883A= , CM000669.2:g.96121883A=	GRCh38
NC_000007.13:g.95751195A= , CM000669.1:g.95751195A=	GRCh37
NC_000007.12:g.95589131A=	NCBI36
NG_012247.1:g.205265T=
NG_012247.2:g.205265T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1706T= MANE Select	ENSP00000265631.6:p.Ile569=
ENST00000265631.9:c.1706T=	ENSP00000265631.5:p.Ile569=
ENST00000416240.6:c.1709T=	ENSP00000400101.2:p.Ile570=
ENST00000494085.1:n.116T=
NM_001160210.1:c.1709T=	NP_001153682.1:p.Ile570=
NM_014251.2:c.1706T=	NP_055066.1:p.Ile569=
NR_027662.1:n.1781T=
XM_006715831.2:c.1739T=	XP_006715894.1:p.Ile580=
XM_011515728.1:c.854T=	XP_011514030.1:p.Ile285=
XM_006715831.4:c.1739T=	XP_006715894.1:p.Ile580=
XM_017011663.1:c.1697T=	XP_016867152.1:p.Ile566=
XM_017011664.2:c.854T=	XP_016867153.1:p.Ile285=
XM_017011665.1:c.854T=	XP_016867154.1:p.Ile285=
XR_001744525.2:n.1952T=
XR_002956405.1:n.2510T=
NM_014251.3:c.1706T= MANE Select	NP_055066.1:p.Ile569=
NR_027662.2:n.1732T=
NM_001160210.2:c.1709T=	NP_001153682.1:p.Ile570=