Canonical Allele Identifier: CA368263378

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95822403C>T (hg19) ; chr7:g.96193091C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193091C>T , CM000669.2:g.96193091C>T	GRCh38
NC_000007.13:g.95822403C>T , CM000669.1:g.95822403C>T	GRCh37
NC_000007.12:g.95660339C>T	NCBI36
NG_012247.1:g.134057G>A
NG_012247.2:g.134057G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.561G>A MANE Select	ENSP00000265631.6:p.Met187Ile
ENST00000265631.9:c.561G>A	ENSP00000265631.5:p.Met187Ile
ENST00000416240.6:c.561G>A	ENSP00000400101.2:p.Met187Ile
NM_001160210.1:c.561G>A	NP_001153682.1:p.Met187Ile
NM_014251.2:c.561G>A	NP_055066.1:p.Met187Ile
NR_027662.1:n.636G>A
XM_006715831.2:c.594G>A	XP_006715894.1:p.Met198Ile
XM_011515727.1:c.594G>A	XP_011514029.1:p.Met198Ile
XM_006715831.4:c.594G>A	XP_006715894.1:p.Met198Ile
XM_011515727.3:c.594G>A	XP_011514029.1:p.Met198Ile
XM_017011663.1:c.552G>A	XP_016867152.1:p.Met184Ile
XM_017011664.2:c.-198G>A	XP_016867153.1:n.-198G>A
XM_017011665.1:c.-198G>A	XP_016867154.1:n.-198G>A
XR_001744525.2:n.732G>A
XR_002956405.1:n.874G>A
NM_014251.3:c.561G>A MANE Select	NP_055066.1:p.Met187Ile
NR_027662.2:n.587G>A
NM_001160210.2:c.561G>A	NP_001153682.1:p.Met187Ile