Canonical Allele Identifier: CA368263497

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95822461A>G (hg19) ; chr7:g.96193149A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193149A>G , CM000669.2:g.96193149A>G	GRCh38
NC_000007.13:g.95822461A>G , CM000669.1:g.95822461A>G	GRCh37
NC_000007.12:g.95660397A>G	NCBI36
NG_012247.1:g.133999T>C
NG_012247.2:g.133999T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.503T>C MANE Select	ENSP00000265631.6:p.Val168Ala
ENST00000265631.9:c.503T>C	ENSP00000265631.5:p.Val168Ala
ENST00000416240.6:c.503T>C	ENSP00000400101.2:p.Val168Ala
ENST00000472162.2:c.*165T>C	ENSP00000473505.1:n.*165T>C
NM_001160210.1:c.503T>C	NP_001153682.1:p.Val168Ala
NM_014251.2:c.503T>C	NP_055066.1:p.Val168Ala
NR_027662.1:n.578T>C
XM_006715831.2:c.536T>C	XP_006715894.1:p.Val179Ala
XM_011515727.1:c.536T>C	XP_011514029.1:p.Val179Ala
XM_006715831.4:c.536T>C	XP_006715894.1:p.Val179Ala
XM_011515727.3:c.536T>C	XP_011514029.1:p.Val179Ala
XM_017011663.1:c.494T>C	XP_016867152.1:p.Val165Ala
XM_017011664.2:c.-256T>C	XP_016867153.1:n.-256T>C
XM_017011665.1:c.-256T>C	XP_016867154.1:n.-256T>C
XR_001744525.2:n.674T>C
XR_002956405.1:n.816T>C
NM_014251.3:c.503T>C MANE Select	NP_055066.1:p.Val168Ala
NR_027662.2:n.529T>C
NM_001160210.2:c.503T>C	NP_001153682.1:p.Val168Ala