Canonical Allele Identifier: CA351622
Community Standard Title: NM_001379210.1(SLC25A26):c.305C>T (p.Ala102Val)
Gene: SLC25A26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.66262055C>T , CM000665.2:g.66262055C>T GRCh38
NC_000003.11:g.66312479C>T , CM000665.1:g.66312479C>T GRCh37
NC_000003.10:g.66395169C>T NCBI36
NG_054637.1:g.133446C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001379210.1:c.305C>T MANE Select NP_001366139.1:p.Ala102Val
ENST00000354883.11:c.305C>T MANE Select ENSP00000346955.6:p.Ala102Val
NM_001164796.1:c.41C>T NP_001158268.1:p.Ala14Val
NM_001350991.1:c.305C>T NP_001337920.1:p.Ala102Val
NM_001350992.1:c.41C>T NP_001337921.1:p.Ala14Val
NM_001350993.1:c.41C>T NP_001337922.1:p.Ala14Val
NM_001400705.1:c.305C>T NP_001387634.1:p.Ala102Val
NM_001400707.1:c.305C>T NP_001387636.1:p.Ala102Val
NM_001400709.1:c.41C>T NP_001387638.1:p.Ala14Val
NM_001400711.1:c.41C>T NP_001387640.1:p.Ala14Val
NM_001400714.1:c.41C>T NP_001387643.1:p.Ala14Val
NM_173471.3:c.305C>T NP_775742.4:p.Ala102Val
NM_173471.4:c.305C>T NP_775742.4:p.Ala102Val
NR_028475.1:n.501C>T
NR_174566.1:n.399C>T
NR_174567.1:n.399C>T
NR_174568.1:n.399C>T
NR_174569.1:n.242C>T
NR_174570.1:n.399C>T
NR_174571.1:n.399C>T
NR_174572.1:n.369C>T
NR_174573.1:n.242C>T
NR_174574.1:n.242C>T
NR_174575.1:n.486C>T
NR_174576.1:n.399C>T
NR_174577.1:n.242C>T
NR_174578.1:n.242C>T
NR_174579.1:n.242C>T
ENST00000336733.10:c.41C>T ENSP00000336801.5:p.Ala14Val
ENST00000354883.10:c.305C>T ENSP00000346955.6:p.Ala102Val
ENST00000413054.5:c.41C>T ENSP00000415304.2:p.Ala14Val
ENST00000464350.6:c.41C>T ENSP00000432574.2:p.Ala14Val
ENST00000483224.5:c.115C>T
ENST00000484768.1:n.61C>T
ENST00000676754.1:c.305C>T ENSP00000504323.1:p.Ala102Val
ENST00000686445.1:c.41C>T ENSP00000509085.1:p.Ala14Val
ENST00000686511.1:c.41C>T ENSP00000509933.1:p.Ala14Val
ENST00000687663.1:n.411C>T
ENST00000688696.1:c.38C>T ENSP00000509851.1:p.Ala13Val
ENST00000689520.1:c.41C>T ENSP00000509413.1:p.Ala14Val
ENST00000690560.1:c.56C>T ENSP00000509947.1:p.Ala19Val
ENST00000690634.1:c.41C>T ENSP00000510529.1:p.Ala14Val
ENST00000691166.1:n.403C>T
ENST00000691461.1:c.41C>T ENSP00000510022.1:p.Ala14Val
ENST00000691525.1:c.41C>T ENSP00000510274.1:p.Ala14Val
ENST00000691582.1:c.305C>T ENSP00000510010.1:p.Ala102Val
ENST00000691603.1:n.318C>T
ENST00000693385.1:c.36+18743C>T ENSP00000509739.1:n.36+18743C>T
XM_006712956.1:c.305C>T XP_006713019.1:p.Ala102Val
XM_006712956.2:c.305C>T XP_006713019.1:p.Ala102Val
XM_006712957.2:c.305C>T XP_006713020.1:p.Ala102Val
XM_011533327.1:c.41C>T XP_011531629.1:p.Ala14Val
XM_011533327.2:c.41C>T XP_011531629.1:p.Ala14Val
XM_011533328.1:c.305C>T XP_011531630.1:p.Ala102Val
XM_011533328.2:c.305C>T XP_011531630.1:p.Ala102Val
XM_017005674.1:c.41C>T XP_016861163.1:p.Ala14Val
XM_024453335.1:c.305C>T XP_024309103.1:p.Ala102Val
XR_001739995.1:n.231C>T
XR_001739996.2:n.399C>T
XR_002959488.1:n.388C>T
XR_427246.1:n.614C>T
XR_427246.2:n.388C>T
XR_940366.1:n.399C>T
XR_940366.3:n.399C>T
XR_940367.1:n.399C>T
XR_940367.3:n.399C>T
XR_940368.1:n.614C>T
XR_940368.2:n.388C>T