Canonical Allele Identifier: CA368262236

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95818653G>T (hg19) ; chr7:g.96189341G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189341G>T , CM000669.2:g.96189341G>T	GRCh38
NC_000007.13:g.95818653G>T , CM000669.1:g.95818653G>T	GRCh37
NC_000007.12:g.95656589G>T	NCBI36
NG_012247.1:g.137807C>A
NG_012247.2:g.137807C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.886C>A MANE Select	ENSP00000265631.6:p.Leu296Met
ENST00000265631.9:c.886C>A	ENSP00000265631.5:p.Leu296Met
ENST00000416240.6:c.886C>A	ENSP00000400101.2:p.Leu296Met
ENST00000484495.5:n.39C>A
NM_001160210.1:c.886C>A	NP_001153682.1:p.Leu296Met
NM_014251.2:c.886C>A	NP_055066.1:p.Leu296Met
NR_027662.1:n.961C>A
XM_006715831.2:c.919C>A	XP_006715894.1:p.Leu307Met
XM_011515727.1:c.919C>A	XP_011514029.1:p.Leu307Met
XM_011515728.1:c.34C>A	XP_011514030.1:p.Leu12Met
XM_006715831.4:c.919C>A	XP_006715894.1:p.Leu307Met
XM_011515727.3:c.919C>A	XP_011514029.1:p.Leu307Met
XM_017011663.1:c.877C>A	XP_016867152.1:p.Leu293Met
XM_017011664.2:c.34C>A	XP_016867153.1:p.Leu12Met
XM_017011665.1:c.34C>A	XP_016867154.1:p.Leu12Met
XR_001744525.2:n.1057C>A
XR_002956405.1:n.1199C>A
NM_014251.3:c.886C>A MANE Select	NP_055066.1:p.Leu296Met
NR_027662.2:n.912C>A
NM_001160210.2:c.886C>A	NP_001153682.1:p.Leu296Met