Canonical Allele Identifier: CA2683824741

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96121904-A-ACTC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121906_96121908dup , CM000669.2:g.96121906_96121908dup	GRCh38
NC_000007.13:g.95751218_95751220dup , CM000669.1:g.95751218_95751220dup	GRCh37
NC_000007.12:g.95589154_95589156dup	NCBI36
NG_012247.1:g.205241_205243dup
NG_012247.2:g.205241_205243dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1682_1684dup MANE Select	ENSP00000265631.6:p.Gly561_Val562insGly
ENST00000265631.9:c.1682_1684dup	ENSP00000265631.5:p.Gly561_Val562insGly
ENST00000416240.6:c.1685_1687dup	ENSP00000400101.2:p.Gly562_Val563insGly
ENST00000494085.1:n.92_94dup
NM_001160210.1:c.1685_1687dup	NP_001153682.1:p.Gly562_Val563insGly
NM_014251.2:c.1682_1684dup	NP_055066.1:p.Gly561_Val562insGly
NR_027662.1:n.1757_1759dup
XM_006715831.2:c.1715_1717dup	XP_006715894.1:p.Gly572_Val573insGly
XM_011515728.1:c.830_832dup	XP_011514030.1:p.Gly277_Val278insGly
XM_006715831.4:c.1715_1717dup	XP_006715894.1:p.Gly572_Val573insGly
XM_017011663.1:c.1673_1675dup	XP_016867152.1:p.Gly558_Val559insGly
XM_017011664.2:c.830_832dup	XP_016867153.1:p.Gly277_Val278insGly
XM_017011665.1:c.830_832dup	XP_016867154.1:p.Gly277_Val278insGly
XR_001744525.2:n.1928_1930dup
XR_002956405.1:n.2486_2488dup
NM_014251.3:c.1682_1684dup MANE Select	NP_055066.1:p.Gly561_Val562insGly
NR_027662.2:n.1708_1710dup
NM_001160210.2:c.1685_1687dup	NP_001153682.1:p.Gly562_Val563insGly