Canonical Allele Identifier: CA576707875

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1336262768
• gnomAD v2: 7-95818862-TC-T
• gnomAD v3: 7-96189550-TC-T
• gnomAD v4: 7-96189550-TC-T
• MyVariant Identifiers: chr7:g.95818863del (hg19) ; chr7:g.96189551del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189552del , CM000669.2:g.96189552del	GRCh38
NC_000007.13:g.95818864del , CM000669.1:g.95818864del	GRCh37
NC_000007.12:g.95656800del	NCBI36
NG_012247.1:g.137597del
NG_012247.2:g.137597del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+30del MANE Select	ENSP00000265631.6:n.848+30del
ENST00000265631.9:c.848+30del	ENSP00000265631.5:n.848+30del
ENST00000416240.6:c.848+30del	ENSP00000400101.2:n.848+30del
NM_001160210.1:c.848+30del	NP_001153682.1:n.848+30del
NM_014251.2:c.848+30del	NP_055066.1:n.848+30del
NR_027662.1:n.923+30del
XM_006715831.2:c.881+30del	XP_006715894.1:n.881+30del
XM_011515727.1:c.881+30del	XP_011514029.1:n.881+30del
XM_011515728.1:c.-4-173del	XP_011514030.1:n.-4-173del
XM_006715831.4:c.881+30del	XP_006715894.1:n.881+30del
XM_011515727.3:c.881+30del	XP_011514029.1:n.881+30del
XM_017011663.1:c.839+30del	XP_016867152.1:n.839+30del
XM_017011664.2:c.-4-173del	XP_016867153.1:n.-4-173del
XM_017011665.1:c.-4-173del	XP_016867154.1:n.-4-173del
XR_001744525.2:n.1019+30del
XR_002956405.1:n.1161+30del
NM_014251.3:c.848+30del MANE Select	NP_055066.1:n.848+30del
NR_027662.2:n.874+30del
NM_001160210.2:c.848+30del	NP_001153682.1:n.848+30del