Canonical Allele Identifier: CA844156100

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1169212614
• MyVariant Identifiers: chr7:g.95750864C>G (hg19) ; chr7:g.96121552C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121552C>G , CM000669.2:g.96121552C>G	GRCh38
NC_000007.13:g.95750864C>G , CM000669.1:g.95750864C>G	GRCh37
NC_000007.12:g.95588800C>G	NCBI36
NG_012247.1:g.205596G>C
NG_012247.2:g.205596G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1841+103G>C MANE Select	ENSP00000265631.6:n.1841+103G>C
ENST00000265631.9:c.1841+103G>C	ENSP00000265631.5:n.1841+103G>C
ENST00000416240.6:c.1844+103G>C	ENSP00000400101.2:n.1844+103G>C
ENST00000494085.1:n.344+103G>C
NM_001160210.1:c.1844+103G>C	NP_001153682.1:n.1844+103G>C
NM_014251.2:c.1841+103G>C	NP_055066.1:n.1841+103G>C
NR_027662.1:n.1916+103G>C
XM_006715831.2:c.1874+103G>C	XP_006715894.1:n.1874+103G>C
XM_011515728.1:c.989+103G>C	XP_011514030.1:n.989+103G>C
XM_006715831.4:c.1874+103G>C	XP_006715894.1:n.1874+103G>C
XM_017011663.1:c.1832+103G>C	XP_016867152.1:n.1832+103G>C
XM_017011664.2:c.989+103G>C	XP_016867153.1:n.989+103G>C
XM_017011665.1:c.989+103G>C	XP_016867154.1:n.989+103G>C
XR_001744525.2:n.2087+103G>C
XR_002956405.1:n.2645+103G>C
NM_014251.3:c.1841+103G>C MANE Select	NP_055066.1:n.1841+103G>C
NR_027662.2:n.1867+103G>C
NM_001160210.2:c.1844+103G>C	NP_001153682.1:n.1844+103G>C