Canonical Allele Identifier: CA2483626

Gene: SLC25A26

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.66243202G>T , CM000665.2:g.66243202G>T	GRCh38
NC_000003.11:g.66293626G>T , CM000665.1:g.66293626G>T	GRCh37
NC_000003.10:g.66376317G>T	NCBI36
NG_054637.1:g.114593G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001379210.1:c.191-1G>T MANE Select	NP_001366139.1:n.191-1G>T
ENST00000354883.11:c.191-1G>T MANE Select	ENSP00000346955.6:n.191-1G>T
NM_001164796.1:c.-74-1G>T	NP_001158268.1:n.-74-1G>T
NM_001350991.1:c.191-1G>T	NP_001337920.1:n.191-1G>T
NM_001350992.1:c.-74-1G>T	NP_001337921.1:n.-74-1G>T
NM_001350993.1:c.-74-1G>T	NP_001337922.1:n.-74-1G>T
NM_001400705.1:c.191-1G>T	NP_001387634.1:n.191-1G>T
NM_001400707.1:c.191-1G>T	NP_001387636.1:n.191-1G>T
NM_001400709.1:c.-74-1G>T	NP_001387638.1:n.-74-1G>T
NM_001400711.1:c.-74-1G>T	NP_001387640.1:n.-74-1G>T
NM_001400714.1:c.-74-1G>T	NP_001387643.1:n.-74-1G>T
NM_173471.3:c.191-1G>T	NP_775742.4:n.191-1G>T
NM_173471.4:c.191-1G>T	NP_775742.4:n.191-1G>T
NR_028475.1:n.387-1G>T
NR_174566.1:n.285-1G>T
NR_174567.1:n.285-1G>T
NR_174568.1:n.285-1G>T
NR_174569.1:n.128-1G>T
NR_174570.1:n.285-1G>T
NR_174571.1:n.285-1G>T
NR_174572.1:n.255-1G>T
NR_174573.1:n.128-1G>T
NR_174574.1:n.128-1G>T
NR_174575.1:n.372-1G>T
NR_174576.1:n.285-1G>T
NR_174577.1:n.128-1G>T
NR_174578.1:n.128-1G>T
NR_174579.1:n.128-1G>T
ENST00000336733.10:c.-74-1G>T	ENSP00000336801.5:n.-74-1G>T
ENST00000354883.10:c.191-1G>T	ENSP00000346955.6:n.191-1G>T
ENST00000464350.6:c.-74-1G>T	ENSP00000432574.2:n.-74-1G>T
ENST00000676754.1:c.191-1G>T	ENSP00000504323.1:n.191-1G>T
ENST00000686445.1:c.-74-1G>T	ENSP00000509085.1:n.-74-1G>T
ENST00000686511.1:c.-74-1G>T	ENSP00000509933.1:n.-74-1G>T
ENST00000687663.1:n.297-1G>T
ENST00000688696.1:c.34-18849G>T	ENSP00000509851.1:n.34-18849G>T
ENST00000689520.1:c.-74-1G>T	ENSP00000509413.1:n.-74-1G>T
ENST00000690560.1:c.51+6502G>T	ENSP00000509947.1:n.51+6502G>T
ENST00000690634.1:c.-74-1G>T	ENSP00000510529.1:n.-74-1G>T
ENST00000691166.1:n.289-1G>T
ENST00000691461.1:c.-74-1G>T	ENSP00000510022.1:n.-74-1G>T
ENST00000691525.1:c.-74-1G>T	ENSP00000510274.1:n.-74-1G>T
ENST00000691582.1:c.191-1G>T	ENSP00000510010.1:n.191-1G>T
ENST00000691603.1:n.204-1G>T
ENST00000693385.1:c.-74-1G>T	ENSP00000509739.1:n.-74-1G>T
XM_006712956.1:c.191-1G>T	XP_006713019.1:n.191-1G>T
XM_006712956.2:c.191-1G>T	XP_006713019.1:n.191-1G>T
XM_006712957.2:c.191-1G>T	XP_006713020.1:n.191-1G>T
XM_011533327.1:c.-74-1G>T	XP_011531629.1:n.-74-1G>T
XM_011533327.2:c.-74-1G>T	XP_011531629.1:n.-74-1G>T
XM_011533328.1:c.191-1G>T	XP_011531630.1:n.191-1G>T
XM_011533328.2:c.191-1G>T	XP_011531630.1:n.191-1G>T
XM_017005674.1:c.-74-1G>T	XP_016861163.1:n.-74-1G>T
XM_024453335.1:c.191-1G>T	XP_024309103.1:n.191-1G>T
XR_001739995.1:n.117-1G>T
XR_001739996.2:n.285-1G>T
XR_002959488.1:n.274-1G>T
XR_427246.1:n.500-1G>T
XR_427246.2:n.274-1G>T
XR_940366.1:n.285-1G>T
XR_940366.3:n.285-1G>T
XR_940367.1:n.285-1G>T
XR_940367.3:n.285-1G>T
XR_940368.1:n.500-1G>T
XR_940368.2:n.274-1G>T