Canonical Allele Identifier: CA2483916

Gene: SLC25A26

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.66377810C>A , CM000665.2:g.66377810C>A	GRCh38
NC_000003.11:g.66428234C>A , CM000665.1:g.66428234C>A	GRCh37
NC_000003.10:g.66510924C>A	NCBI36
NG_054637.1:g.249201C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001379210.1:c.*3C>A MANE Select	NP_001366139.1:n.*3C>A
ENST00000354883.11:c.*3C>A MANE Select	ENSP00000346955.6:n.*3C>A
NM_001164796.1:c.*3C>A	NP_001158268.1:n.*3C>A
NM_001350991.1:c.*3C>A	NP_001337920.1:n.*3C>A
NM_001350992.1:c.*3C>A	NP_001337921.1:n.*3C>A
NM_001350993.1:c.*3C>A	NP_001337922.1:n.*3C>A
NM_001400705.1:c.*143C>A	NP_001387634.1:n.*143C>A
NM_001400707.1:c.*3C>A	NP_001387636.1:n.*3C>A
NM_001400709.1:c.*143C>A	NP_001387638.1:n.*143C>A
NM_001400711.1:c.*3C>A	NP_001387640.1:n.*3C>A
NM_001400714.1:c.*3C>A	NP_001387643.1:n.*3C>A
NM_173471.3:c.*3C>A	NP_775742.4:n.*3C>A
NM_173471.4:c.*3C>A	NP_775742.4:n.*3C>A
NR_028475.1:n.1109C>A
NR_174566.1:n.852C>A
NR_174567.1:n.922C>A
NR_174568.1:n.976C>A
NR_174569.1:n.765C>A
NR_174570.1:n.877C>A
NR_174571.1:n.807C>A
NR_174572.1:n.822C>A
NR_174573.1:n.650C>A
NR_174574.1:n.819C>A
NR_174575.1:n.1009C>A
NR_174576.1:n.1007C>A
NR_174577.1:n.765C>A
NR_174578.1:n.850C>A
NR_174579.1:n.650C>A
ENST00000336733.10:c.*3C>A	ENSP00000336801.5:n.*3C>A
ENST00000354883.10:c.*3C>A	ENSP00000346955.6:n.*3C>A
ENST00000413054.5:c.*143C>A	ENSP00000415304.2:n.*143C>A
ENST00000464350.6:c.*357C>A	ENSP00000432574.2:n.*357C>A
ENST00000483224.5:c.723C>A
ENST00000676754.1:c.*3C>A	ENSP00000504323.1:n.*3C>A
ENST00000685460.1:n.609C>A
ENST00000686445.1:c.*227C>A	ENSP00000509085.1:n.*227C>A
ENST00000686511.1:c.*3C>A	ENSP00000509933.1:n.*3C>A
ENST00000688696.1:c.*3C>A	ENSP00000509851.1:n.*3C>A
ENST00000689520.1:c.*3C>A	ENSP00000509413.1:n.*3C>A
ENST00000690522.1:n.952C>A
ENST00000690560.1:c.*227C>A	ENSP00000509947.1:n.*227C>A
ENST00000690634.1:c.*227C>A	ENSP00000510529.1:n.*227C>A
ENST00000691461.1:c.*3C>A	ENSP00000510022.1:n.*3C>A
ENST00000691525.1:c.*287C>A	ENSP00000510274.1:n.*287C>A
ENST00000691582.1:c.*1485C>A	ENSP00000510010.1:n.*1485C>A
ENST00000693385.1:c.*3C>A	ENSP00000509739.1:n.*3C>A
XM_006712956.1:c.*3C>A	XP_006713019.1:n.*3C>A
XM_006712956.2:c.*3C>A	XP_006713019.1:n.*3C>A
XM_011533327.1:c.*3C>A	XP_011531629.1:n.*3C>A
XM_011533327.2:c.*3C>A	XP_011531629.1:n.*3C>A
XM_017005674.1:c.*3C>A	XP_016861163.1:n.*3C>A
XR_001739995.1:n.754C>A
XR_001739996.2:n.976C>A
XR_002959488.1:n.866C>A
XR_940366.1:n.922C>A
XR_940366.3:n.922C>A
XR_940367.1:n.852C>A
XR_940367.3:n.852C>A
XR_940368.1:n.1022C>A
XR_940368.2:n.796C>A