Canonical Allele Identifier: CA576347388

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1283806774
• gnomAD v2: 7-95751460-G-GC
• gnomAD v3: 7-96122148-G-GC
• gnomAD v4: 7-96122148-G-GC
• MyVariant Identifiers: chr7:g.95751460_95751461insC (hg19) ; chr7:g.96122148_96122149insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96122150dup , CM000669.2:g.96122150dup	GRCh38
NC_000007.13:g.95751462dup , CM000669.1:g.95751462dup	GRCh37
NC_000007.12:g.95589398dup	NCBI36
NG_012247.1:g.204999dup
NG_012247.2:g.204999dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1592-152dup MANE Select	ENSP00000265631.6:n.1592-152dup
ENST00000265631.9:c.1592-152dup	ENSP00000265631.5:n.1592-152dup
ENST00000416240.6:c.1595-152dup	ENSP00000400101.2:n.1595-152dup
NM_001160210.1:c.1595-152dup	NP_001153682.1:n.1595-152dup
NM_014251.2:c.1592-152dup	NP_055066.1:n.1592-152dup
NR_027662.1:n.1667-152dup
XM_006715831.2:c.1625-152dup	XP_006715894.1:n.1625-152dup
XM_011515728.1:c.740-152dup	XP_011514030.1:n.740-152dup
XM_006715831.4:c.1625-152dup	XP_006715894.1:n.1625-152dup
XM_017011663.1:c.1583-152dup	XP_016867152.1:n.1583-152dup
XM_017011664.2:c.740-152dup	XP_016867153.1:n.740-152dup
XM_017011665.1:c.740-152dup	XP_016867154.1:n.740-152dup
XR_001744525.2:n.1838-152dup
XR_002956405.1:n.2396-152dup
NM_014251.3:c.1592-152dup MANE Select	NP_055066.1:n.1592-152dup
NR_027662.2:n.1618-152dup
NM_001160210.2:c.1595-152dup	NP_001153682.1:n.1595-152dup