Canonical Allele Identifier: CA2683824711

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96121787-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121792del , CM000669.2:g.96121792del	GRCh38
NC_000007.13:g.95751104del , CM000669.1:g.95751104del	GRCh37
NC_000007.12:g.95589040del	NCBI36
NG_012247.1:g.205360del
NG_012247.2:g.205360del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1751-43del MANE Select	ENSP00000265631.6:n.1751-43del
ENST00000265631.9:c.1751-43del	ENSP00000265631.5:n.1751-43del
ENST00000416240.6:c.1754-43del	ENSP00000400101.2:n.1754-43del
ENST00000494085.1:n.211del
NM_001160210.1:c.1754-43del	NP_001153682.1:n.1754-43del
NM_014251.2:c.1751-43del	NP_055066.1:n.1751-43del
NR_027662.1:n.1826-43del
XM_006715831.2:c.1784-43del	XP_006715894.1:n.1784-43del
XM_011515728.1:c.899-43del	XP_011514030.1:n.899-43del
XM_006715831.4:c.1784-43del	XP_006715894.1:n.1784-43del
XM_017011663.1:c.1742-43del	XP_016867152.1:n.1742-43del
XM_017011664.2:c.899-43del	XP_016867153.1:n.899-43del
XM_017011665.1:c.899-43del	XP_016867154.1:n.899-43del
XR_001744525.2:n.1997-43del
XR_002956405.1:n.2555-43del
NM_014251.3:c.1751-43del MANE Select	NP_055066.1:n.1751-43del
NR_027662.2:n.1777-43del
NM_001160210.2:c.1754-43del	NP_001153682.1:n.1754-43del