Canonical Allele Identifier: CA368263420

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95822422A>T (hg19) ; chr7:g.96193110A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193110A>T , CM000669.2:g.96193110A>T	GRCh38
NC_000007.13:g.95822422A>T , CM000669.1:g.95822422A>T	GRCh37
NC_000007.12:g.95660358A>T	NCBI36
NG_012247.1:g.134038T>A
NG_012247.2:g.134038T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.542T>A MANE Select	ENSP00000265631.6:p.Ile181Asn
ENST00000265631.9:c.542T>A	ENSP00000265631.5:p.Ile181Asn
ENST00000416240.6:c.542T>A	ENSP00000400101.2:p.Ile181Asn
NM_001160210.1:c.542T>A	NP_001153682.1:p.Ile181Asn
NM_014251.2:c.542T>A	NP_055066.1:p.Ile181Asn
NR_027662.1:n.617T>A
XM_006715831.2:c.575T>A	XP_006715894.1:p.Ile192Asn
XM_011515727.1:c.575T>A	XP_011514029.1:p.Ile192Asn
XM_006715831.4:c.575T>A	XP_006715894.1:p.Ile192Asn
XM_011515727.3:c.575T>A	XP_011514029.1:p.Ile192Asn
XM_017011663.1:c.533T>A	XP_016867152.1:p.Ile178Asn
XM_017011664.2:c.-217T>A	XP_016867153.1:n.-217T>A
XM_017011665.1:c.-217T>A	XP_016867154.1:n.-217T>A
XR_001744525.2:n.713T>A
XR_002956405.1:n.855T>A
NM_014251.3:c.542T>A MANE Select	NP_055066.1:p.Ile181Asn
NR_027662.2:n.568T>A
NM_001160210.2:c.542T>A	NP_001153682.1:p.Ile181Asn