Canonical Allele Identifier: CA368257478

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750653C>A (hg19) ; chr7:g.96121341C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121341C>A , CM000669.2:g.96121341C>A	GRCh38
NC_000007.13:g.95750653C>A , CM000669.1:g.95750653C>A	GRCh37
NC_000007.12:g.95588589C>A	NCBI36
NG_012247.1:g.205807G>T
NG_012247.2:g.205807G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1878G>T MANE Select	ENSP00000265631.6:p.Arg626Ser
ENST00000265631.9:c.1878G>T	ENSP00000265631.5:p.Arg626Ser
ENST00000416240.6:c.1881G>T	ENSP00000400101.2:p.Arg627Ser
ENST00000494085.1:n.381G>T
NM_001160210.1:c.1881G>T	NP_001153682.1:p.Arg627Ser
NM_014251.2:c.1878G>T	NP_055066.1:p.Arg626Ser
NR_027662.1:n.1953G>T
XM_006715831.2:c.1911G>T	XP_006715894.1:p.Arg637Ser
XM_011515728.1:c.1026G>T	XP_011514030.1:p.Arg342Ser
XM_006715831.4:c.1911G>T	XP_006715894.1:p.Arg637Ser
XM_017011663.1:c.1869G>T	XP_016867152.1:p.Arg623Ser
XM_017011664.2:c.1026G>T	XP_016867153.1:p.Arg342Ser
XM_017011665.1:c.1026G>T	XP_016867154.1:p.Arg342Ser
XR_001744525.2:n.2124G>T
XR_002956405.1:n.2682G>T
NM_014251.3:c.1878G>T MANE Select	NP_055066.1:p.Arg626Ser
NR_027662.2:n.1904G>T
NM_001160210.2:c.1881G>T	NP_001153682.1:p.Arg627Ser