Canonical Allele Identifier: CA456509960

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750629A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121317A>C , CM000669.2:g.96121317A>C	GRCh38
NC_000007.13:g.95750629A>C , CM000669.1:g.95750629A>C	GRCh37
NC_000007.12:g.95588565A>C	NCBI36
NG_012247.1:g.205831T>G
NG_012247.2:g.205831T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1902T>G MANE Select	ENSP00000265631.6:p.Pro634=
ENST00000265631.9:c.1902T>G	ENSP00000265631.5:p.Pro634=
ENST00000416240.6:c.1905T>G	ENSP00000400101.2:p.Pro635=
ENST00000494085.1:n.405T>G
NM_001160210.1:c.1905T>G	NP_001153682.1:p.Pro635=
NM_014251.2:c.1902T>G	NP_055066.1:p.Pro634=
NR_027662.1:n.1977T>G
XM_006715831.2:c.1935T>G	XP_006715894.1:p.Pro645=
XM_011515728.1:c.1050T>G	XP_011514030.1:p.Pro350=
XM_006715831.4:c.1935T>G	XP_006715894.1:p.Pro645=
XM_017011663.1:c.1893T>G	XP_016867152.1:p.Pro631=
XM_017011664.2:c.1050T>G	XP_016867153.1:p.Pro350=
XM_017011665.1:c.1050T>G	XP_016867154.1:p.Pro350=
XR_001744525.2:n.2148T>G
XR_002956405.1:n.2706T>G
NM_014251.3:c.1902T>G MANE Select	NP_055066.1:p.Pro634=
NR_027662.2:n.1928T>G
NM_001160210.2:c.1905T>G	NP_001153682.1:p.Pro635=