Canonical Allele Identifier: CA1727580505

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189529_96189532delinsACCT , CM000669.2:g.96189529_96189532delinsACCT	GRCh38
NC_000007.13:g.95818841_95818844delinsACCT , CM000669.1:g.95818841_95818844delinsACCT	GRCh37
NC_000007.12:g.95656777_95656780delinsACCT	NCBI36
NG_012247.1:g.137616_137619delinsAGGT
NG_012247.2:g.137616_137619delinsAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+49_848+52delinsAGGT MANE Select	ENSP00000265631.6:n.848+49_848+52delinsAGGT
ENST00000265631.9:c.848+49_848+52delinsAGGT	ENSP00000265631.5:n.848+49_848+52delinsAGGT
ENST00000416240.6:c.848+49_848+52delinsAGGT	ENSP00000400101.2:n.848+49_848+52delinsAGGT
NM_001160210.1:c.848+49_848+52delinsAGGT	NP_001153682.1:n.848+49_848+52delinsAGGT
NM_014251.2:c.848+49_848+52delinsAGGT	NP_055066.1:n.848+49_848+52delinsAGGT
NR_027662.1:n.923+49_923+52delinsAGGT
XM_006715831.2:c.881+49_881+52delinsAGGT	XP_006715894.1:n.881+49_881+52delinsAGGT
XM_011515727.1:c.881+49_881+52delinsAGGT	XP_011514029.1:n.881+49_881+52delinsAGGT
XM_011515728.1:c.-4-154_-4-151delinsAGGT	XP_011514030.1:n.-4-154_-4-151delinsAGGT
XM_006715831.4:c.881+49_881+52delinsAGGT	XP_006715894.1:n.881+49_881+52delinsAGGT
XM_011515727.3:c.881+49_881+52delinsAGGT	XP_011514029.1:n.881+49_881+52delinsAGGT
XM_017011663.1:c.839+49_839+52delinsAGGT	XP_016867152.1:n.839+49_839+52delinsAGGT
XM_017011664.2:c.-4-154_-4-151delinsAGGT	XP_016867153.1:n.-4-154_-4-151delinsAGGT
XM_017011665.1:c.-4-154_-4-151delinsAGGT	XP_016867154.1:n.-4-154_-4-151delinsAGGT
XR_001744525.2:n.1019+49_1019+52delinsAGGT
XR_002956405.1:n.1161+49_1161+52delinsAGGT
NM_014251.3:c.848+49_848+52delinsAGGT MANE Select	NP_055066.1:n.848+49_848+52delinsAGGT
NR_027662.2:n.874+49_874+52delinsAGGT
NM_001160210.2:c.848+49_848+52delinsAGGT	NP_001153682.1:n.848+49_848+52delinsAGGT