Canonical Allele Identifier: CA368257361

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750625G>A (hg19) ; chr7:g.96121313G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121313G>A , CM000669.2:g.96121313G>A	GRCh38
NC_000007.13:g.95750625G>A , CM000669.1:g.95750625G>A	GRCh37
NC_000007.12:g.95588561G>A	NCBI36
NG_012247.1:g.205835C>T
NG_012247.2:g.205835C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1906C>T MANE Select	ENSP00000265631.6:p.His636Tyr
ENST00000265631.9:c.1906C>T	ENSP00000265631.5:p.His636Tyr
ENST00000416240.6:c.1909C>T	ENSP00000400101.2:p.His637Tyr
ENST00000494085.1:n.409C>T
NM_001160210.1:c.1909C>T	NP_001153682.1:p.His637Tyr
NM_014251.2:c.1906C>T	NP_055066.1:p.His636Tyr
NR_027662.1:n.1981C>T
XM_006715831.2:c.1939C>T	XP_006715894.1:p.His647Tyr
XM_011515728.1:c.1054C>T	XP_011514030.1:p.His352Tyr
XM_006715831.4:c.1939C>T	XP_006715894.1:p.His647Tyr
XM_017011663.1:c.1897C>T	XP_016867152.1:p.His633Tyr
XM_017011664.2:c.1054C>T	XP_016867153.1:p.His352Tyr
XM_017011665.1:c.1054C>T	XP_016867154.1:p.His352Tyr
XR_001744525.2:n.2152C>T
XR_002956405.1:n.2710C>T
NM_014251.3:c.1906C>T MANE Select	NP_055066.1:p.His636Tyr
NR_027662.2:n.1932C>T
NM_001160210.2:c.1909C>T	NP_001153682.1:p.His637Tyr