Canonical Allele Identifier: CA1727580326

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189393_96189394delinsCA , CM000669.2:g.96189393_96189394delinsCA	GRCh38
NC_000007.13:g.95818705_95818706delinsCA , CM000669.1:g.95818705_95818706delinsCA	GRCh37
NC_000007.12:g.95656641_95656642delinsCA	NCBI36
NG_012247.1:g.137754_137755delinsTG
NG_012247.2:g.137754_137755delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.849-16_849-15delinsTG MANE Select	ENSP00000265631.6:n.849-16_849-15delinsTG
ENST00000265631.9:c.849-16_849-15delinsTG	ENSP00000265631.5:n.849-16_849-15delinsTG
ENST00000416240.6:c.849-16_849-15delinsTG	ENSP00000400101.2:n.849-16_849-15delinsTG
NM_001160210.1:c.849-16_849-15delinsTG	NP_001153682.1:n.849-16_849-15delinsTG
NM_014251.2:c.849-16_849-15delinsTG	NP_055066.1:n.849-16_849-15delinsTG
NR_027662.1:n.924-16_924-15delinsTG
XM_006715831.2:c.882-16_882-15delinsTG	XP_006715894.1:n.882-16_882-15delinsTG
XM_011515727.1:c.882-16_882-15delinsTG	XP_011514029.1:n.882-16_882-15delinsTG
XM_011515728.1:c.-4-16_-4-15delinsTG	XP_011514030.1:n.-4-16_-4-15delinsTG
XM_006715831.4:c.882-16_882-15delinsTG	XP_006715894.1:n.882-16_882-15delinsTG
XM_011515727.3:c.882-16_882-15delinsTG	XP_011514029.1:n.882-16_882-15delinsTG
XM_017011663.1:c.840-16_840-15delinsTG	XP_016867152.1:n.840-16_840-15delinsTG
XM_017011664.2:c.-4-16_-4-15delinsTG	XP_016867153.1:n.-4-16_-4-15delinsTG
XM_017011665.1:c.-4-16_-4-15delinsTG	XP_016867154.1:n.-4-16_-4-15delinsTG
XR_001744525.2:n.1020-16_1020-15delinsTG
XR_002956405.1:n.1162-16_1162-15delinsTG
NM_014251.3:c.849-16_849-15delinsTG MANE Select	NP_055066.1:n.849-16_849-15delinsTG
NR_027662.2:n.875-16_875-15delinsTG
NM_001160210.2:c.849-16_849-15delinsTG	NP_001153682.1:n.849-16_849-15delinsTG