Canonical Allele Identifier: CA368257480

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750654C>A (hg19) ; chr7:g.96121342C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121342C>A , CM000669.2:g.96121342C>A	GRCh38
NC_000007.13:g.95750654C>A , CM000669.1:g.95750654C>A	GRCh37
NC_000007.12:g.95588590C>A	NCBI36
NG_012247.1:g.205806G>T
NG_012247.2:g.205806G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1877G>T MANE Select	ENSP00000265631.6:p.Arg626Met
ENST00000265631.9:c.1877G>T	ENSP00000265631.5:p.Arg626Met
ENST00000416240.6:c.1880G>T	ENSP00000400101.2:p.Arg627Met
ENST00000494085.1:n.380G>T
NM_001160210.1:c.1880G>T	NP_001153682.1:p.Arg627Met
NM_014251.2:c.1877G>T	NP_055066.1:p.Arg626Met
NR_027662.1:n.1952G>T
XM_006715831.2:c.1910G>T	XP_006715894.1:p.Arg637Met
XM_011515728.1:c.1025G>T	XP_011514030.1:p.Arg342Met
XM_006715831.4:c.1910G>T	XP_006715894.1:p.Arg637Met
XM_017011663.1:c.1868G>T	XP_016867152.1:p.Arg623Met
XM_017011664.2:c.1025G>T	XP_016867153.1:p.Arg342Met
XM_017011665.1:c.1025G>T	XP_016867154.1:p.Arg342Met
XR_001744525.2:n.2123G>T
XR_002956405.1:n.2681G>T
NM_014251.3:c.1877G>T MANE Select	NP_055066.1:p.Arg626Met
NR_027662.2:n.1903G>T
NM_001160210.2:c.1880G>T	NP_001153682.1:p.Arg627Met