Canonical Allele Identifier: CA368257385

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750631G>A (hg19) ; chr7:g.96121319G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121319G>A , CM000669.2:g.96121319G>A	GRCh38
NC_000007.13:g.95750631G>A , CM000669.1:g.95750631G>A	GRCh37
NC_000007.12:g.95588567G>A	NCBI36
NG_012247.1:g.205829C>T
NG_012247.2:g.205829C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1900C>T MANE Select	ENSP00000265631.6:p.Pro634Ser
ENST00000265631.9:c.1900C>T	ENSP00000265631.5:p.Pro634Ser
ENST00000416240.6:c.1903C>T	ENSP00000400101.2:p.Pro635Ser
ENST00000494085.1:n.403C>T
NM_001160210.1:c.1903C>T	NP_001153682.1:p.Pro635Ser
NM_014251.2:c.1900C>T	NP_055066.1:p.Pro634Ser
NR_027662.1:n.1975C>T
XM_006715831.2:c.1933C>T	XP_006715894.1:p.Pro645Ser
XM_011515728.1:c.1048C>T	XP_011514030.1:p.Pro350Ser
XM_006715831.4:c.1933C>T	XP_006715894.1:p.Pro645Ser
XM_017011663.1:c.1891C>T	XP_016867152.1:p.Pro631Ser
XM_017011664.2:c.1048C>T	XP_016867153.1:p.Pro350Ser
XM_017011665.1:c.1048C>T	XP_016867154.1:p.Pro350Ser
XR_001744525.2:n.2146C>T
XR_002956405.1:n.2704C>T
NM_014251.3:c.1900C>T MANE Select	NP_055066.1:p.Pro634Ser
NR_027662.2:n.1926C>T
NM_001160210.2:c.1903C>T	NP_001153682.1:p.Pro635Ser