Canonical Allele Identifier: CA844156187

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1297566149
• MyVariant Identifiers: chr7:g.95750956_95750958del (hg19) ; chr7:g.96121644_96121646del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121646_96121648del , CM000669.2:g.96121646_96121648del	GRCh38
NC_000007.13:g.95750958_95750960del , CM000669.1:g.95750958_95750960del	GRCh37
NC_000007.12:g.95588894_95588896del	NCBI36
NG_012247.1:g.205502_205504del
NG_012247.2:g.205502_205504del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1841+9_1841+11del MANE Select	ENSP00000265631.6:n.1841+9_1841+11del
ENST00000265631.9:c.1841+9_1841+11del	ENSP00000265631.5:n.1841+9_1841+11del
ENST00000416240.6:c.1844+9_1844+11del	ENSP00000400101.2:n.1844+9_1844+11del
ENST00000494085.1:n.344+9_344+11del
NM_001160210.1:c.1844+9_1844+11del	NP_001153682.1:n.1844+9_1844+11del
NM_014251.2:c.1841+9_1841+11del	NP_055066.1:n.1841+9_1841+11del
NR_027662.1:n.1916+9_1916+11del
XM_006715831.2:c.1874+9_1874+11del	XP_006715894.1:n.1874+9_1874+11del
XM_011515728.1:c.989+9_989+11del	XP_011514030.1:n.989+9_989+11del
XM_006715831.4:c.1874+9_1874+11del	XP_006715894.1:n.1874+9_1874+11del
XM_017011663.1:c.1832+9_1832+11del	XP_016867152.1:n.1832+9_1832+11del
XM_017011664.2:c.989+9_989+11del	XP_016867153.1:n.989+9_989+11del
XM_017011665.1:c.989+9_989+11del	XP_016867154.1:n.989+9_989+11del
XR_001744525.2:n.2087+9_2087+11del
XR_002956405.1:n.2645+9_2645+11del
NM_014251.3:c.1841+9_1841+11del MANE Select	NP_055066.1:n.1841+9_1841+11del
NR_027662.2:n.1867+9_1867+11del
NM_001160210.2:c.1844+9_1844+11del	NP_001153682.1:n.1844+9_1844+11del