Canonical Allele Identifier: CA368257356

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95750624T>G (hg19) ; chr7:g.96121312T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121312T>G , CM000669.2:g.96121312T>G	GRCh38
NC_000007.13:g.95750624T>G , CM000669.1:g.95750624T>G	GRCh37
NC_000007.12:g.95588560T>G	NCBI36
NG_012247.1:g.205836A>C
NG_012247.2:g.205836A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1907A>C MANE Select	ENSP00000265631.6:p.His636Pro
ENST00000265631.9:c.1907A>C	ENSP00000265631.5:p.His636Pro
ENST00000416240.6:c.1910A>C	ENSP00000400101.2:p.His637Pro
ENST00000494085.1:n.410A>C
NM_001160210.1:c.1910A>C	NP_001153682.1:p.His637Pro
NM_014251.2:c.1907A>C	NP_055066.1:p.His636Pro
NR_027662.1:n.1982A>C
XM_006715831.2:c.1940A>C	XP_006715894.1:p.His647Pro
XM_011515728.1:c.1055A>C	XP_011514030.1:p.His352Pro
XM_006715831.4:c.1940A>C	XP_006715894.1:p.His647Pro
XM_017011663.1:c.1898A>C	XP_016867152.1:p.His633Pro
XM_017011664.2:c.1055A>C	XP_016867153.1:p.His352Pro
XM_017011665.1:c.1055A>C	XP_016867154.1:p.His352Pro
XR_001744525.2:n.2153A>C
XR_002956405.1:n.2711A>C
NM_014251.3:c.1907A>C MANE Select	NP_055066.1:p.His636Pro
NR_027662.2:n.1933A>C
NM_001160210.2:c.1910A>C	NP_001153682.1:p.His637Pro