Canonical Allele Identifier: CA368258675

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95751309C>G (hg19) ; chr7:g.96121997C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121997C>G , CM000669.2:g.96121997C>G	GRCh38
NC_000007.13:g.95751309C>G , CM000669.1:g.95751309C>G	GRCh37
NC_000007.12:g.95589245C>G	NCBI36
NG_012247.1:g.205151G>C
NG_012247.2:g.205151G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1592G>C MANE Select	ENSP00000265631.6:p.Gly531Ala
ENST00000265631.9:c.1592G>C	ENSP00000265631.5:p.Gly531Ala
ENST00000416240.6:c.1595G>C	ENSP00000400101.2:p.Gly532Ala
ENST00000494085.1:n.2G>C
NM_001160210.1:c.1595G>C	NP_001153682.1:p.Gly532Ala
NM_014251.2:c.1592G>C	NP_055066.1:p.Gly531Ala
NR_027662.1:n.1667G>C
XM_006715831.2:c.1625G>C	XP_006715894.1:p.Gly542Ala
XM_011515728.1:c.740G>C	XP_011514030.1:p.Gly247Ala
XM_006715831.4:c.1625G>C	XP_006715894.1:p.Gly542Ala
XM_017011663.1:c.1583G>C	XP_016867152.1:p.Gly528Ala
XM_017011664.2:c.740G>C	XP_016867153.1:p.Gly247Ala
XM_017011665.1:c.740G>C	XP_016867154.1:p.Gly247Ala
XR_001744525.2:n.1838G>C
XR_002956405.1:n.2396G>C
NM_014251.3:c.1592G>C MANE Select	NP_055066.1:p.Gly531Ala
NR_027662.2:n.1618G>C
NM_001160210.2:c.1595G>C	NP_001153682.1:p.Gly532Ala