Canonical Allele Identifier: CA1727518755
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96122088_96122089delinsGT , CM000669.2:g.96122088_96122089delinsGT GRCh38
NC_000007.13:g.95751400_95751401delinsGT , CM000669.1:g.95751400_95751401delinsGT GRCh37
NC_000007.12:g.95589336_95589337delinsGT NCBI36
NG_012247.1:g.205059_205060delinsAC
NG_012247.2:g.205059_205060delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.1592-92_1592-91delinsAC MANE Select ENSP00000265631.6:n.1592-92_1592-91delinsAC
ENST00000265631.9:c.1592-92_1592-91delinsAC ENSP00000265631.5:n.1592-92_1592-91delinsAC
ENST00000416240.6:c.1595-92_1595-91delinsAC ENSP00000400101.2:n.1595-92_1595-91delinsAC
NM_001160210.1:c.1595-92_1595-91delinsAC NP_001153682.1:n.1595-92_1595-91delinsAC
NM_014251.2:c.1592-92_1592-91delinsAC NP_055066.1:n.1592-92_1592-91delinsAC
NR_027662.1:n.1667-92_1667-91delinsAC
XM_006715831.2:c.1625-92_1625-91delinsAC XP_006715894.1:n.1625-92_1625-91delinsAC
XM_011515728.1:c.740-92_740-91delinsAC XP_011514030.1:n.740-92_740-91delinsAC
XM_006715831.4:c.1625-92_1625-91delinsAC XP_006715894.1:n.1625-92_1625-91delinsAC
XM_017011663.1:c.1583-92_1583-91delinsAC XP_016867152.1:n.1583-92_1583-91delinsAC
XM_017011664.2:c.740-92_740-91delinsAC XP_016867153.1:n.740-92_740-91delinsAC
XM_017011665.1:c.740-92_740-91delinsAC XP_016867154.1:n.740-92_740-91delinsAC
XR_001744525.2:n.1838-92_1838-91delinsAC
XR_002956405.1:n.2396-92_2396-91delinsAC
NM_014251.3:c.1592-92_1592-91delinsAC MANE Select NP_055066.1:n.1592-92_1592-91delinsAC
NR_027662.2:n.1618-92_1618-91delinsAC
NM_001160210.2:c.1595-92_1595-91delinsAC NP_001153682.1:n.1595-92_1595-91delinsAC