Canonical Allele Identifier: CA368257483

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750655T>A (hg19) ; chr7:g.96121343T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121343T>A , CM000669.2:g.96121343T>A	GRCh38
NC_000007.13:g.95750655T>A , CM000669.1:g.95750655T>A	GRCh37
NC_000007.12:g.95588591T>A	NCBI36
NG_012247.1:g.205805A>T
NG_012247.2:g.205805A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1876A>T MANE Select	ENSP00000265631.6:p.Arg626Trp
ENST00000265631.9:c.1876A>T	ENSP00000265631.5:p.Arg626Trp
ENST00000416240.6:c.1879A>T	ENSP00000400101.2:p.Arg627Trp
ENST00000494085.1:n.379A>T
NM_001160210.1:c.1879A>T	NP_001153682.1:p.Arg627Trp
NM_014251.2:c.1876A>T	NP_055066.1:p.Arg626Trp
NR_027662.1:n.1951A>T
XM_006715831.2:c.1909A>T	XP_006715894.1:p.Arg637Trp
XM_011515728.1:c.1024A>T	XP_011514030.1:p.Arg342Trp
XM_006715831.4:c.1909A>T	XP_006715894.1:p.Arg637Trp
XM_017011663.1:c.1867A>T	XP_016867152.1:p.Arg623Trp
XM_017011664.2:c.1024A>T	XP_016867153.1:p.Arg342Trp
XM_017011665.1:c.1024A>T	XP_016867154.1:p.Arg342Trp
XR_001744525.2:n.2122A>T
XR_002956405.1:n.2680A>T
NM_014251.3:c.1876A>T MANE Select	NP_055066.1:p.Arg626Trp
NR_027662.2:n.1902A>T
NM_001160210.2:c.1879A>T	NP_001153682.1:p.Arg627Trp