Canonical Allele Identifier: CA2683824631

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96121646-G-GATACTTACACTCCTCCAAAATCAATGTAGAACCATCGCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121648_96121688dup , CM000669.2:g.96121648_96121688dup	GRCh38
NC_000007.13:g.95750960_95751000dup , CM000669.1:g.95750960_95751000dup	GRCh37
NC_000007.12:g.95588896_95588936dup	NCBI36
NG_012247.1:g.205461_205501dup
NG_012247.2:g.205461_205501dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1809_1841+8dup
ENST00000265631.9:c.1809_1841+8dup
ENST00000416240.6:c.1812_1844+8dup
ENST00000494085.1:n.312_344+8dup
NM_001160210.1:c.1812_1844+8dup
NM_014251.2:c.1809_1841+8dup
NR_027662.1:n.1884_1916+8dup
XM_006715831.2:c.1842_1874+8dup
XM_011515728.1:c.957_989+8dup
XM_006715831.4:c.1842_1874+8dup
XM_017011663.1:c.1800_1832+8dup
XM_017011664.2:c.957_989+8dup
XM_017011665.1:c.957_989+8dup
XR_001744525.2:n.2055_2087+8dup
XR_002956405.1:n.2613_2645+8dup
NM_014251.3:c.1809_1841+8dup
NR_027662.2:n.1835_1867+8dup
NM_001160210.2:c.1812_1844+8dup