Canonical Allele Identifier: CA2484160

Gene: SLC25A26 LRIG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.66380855C>A , CM000665.2:g.66380855C>A	GRCh38
NC_000003.11:g.66431279C>A , CM000665.1:g.66431279C>A	GRCh37
NC_000003.10:g.66513969C>A	NCBI36
NG_054637.1:g.252246C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691461.1:c.*1045C>A (SLC25A26)	ENSP00000510022.1:n.*1045C>A
ENST00000273261.8:c.2777G>T (LRIG1) MANE Select	ENSP00000273261.3:p.Gly926Val
ENST00000273261.7:c.2777G>T (LRIG1)	ENSP00000273261.3:p.Gly926Val
ENST00000383703.3:c.2708G>T (LRIG1)	ENSP00000373208.3:p.Gly903Val
ENST00000464350.6:c.*1449C>A (SLC25A26)	ENSP00000432574.2:n.*1449C>A
ENST00000495037.1:n.1793G>T (LRIG1)
ENST00000496559.6:n.2159G>T (LRIG1)
NM_015541.2:c.2777G>T (LRIG1)	NP_056356.2:p.Gly926Val
XM_011533578.1:c.2633G>T (LRIG1)	XP_011531880.1:p.Gly878Val
XM_011533579.1:c.1997G>T (LRIG1)	XP_011531881.1:p.Gly666Val
XM_011533578.2:c.2633G>T (LRIG1)	XP_011531880.1:p.Gly878Val
XM_011533579.3:c.1997G>T (LRIG1)	XP_011531881.1:p.Gly666Val
XM_017006134.2:c.2702G>T (LRIG1)	XP_016861623.1:p.Gly901Val
XM_017006135.1:c.2099G>T (LRIG1)	XP_016861624.1:p.Gly700Val
XM_017006136.2:c.1997G>T (LRIG1)	XP_016861625.1:p.Gly666Val
NM_001377344.1:c.2702G>T (LRIG1)	NP_001364273.1:p.Gly901Val
NM_001377345.1:c.1997G>T (LRIG1)	NP_001364274.1:p.Gly666Val
NM_001377346.1:c.1997G>T (LRIG1)	NP_001364275.1:p.Gly666Val
NM_001377347.1:c.1775G>T (LRIG1)	NP_001364276.1:p.Gly592Val
NM_001377348.1:c.1748G>T (LRIG1)	NP_001364277.1:p.Gly583Val
NM_001377349.1:c.1493G>T (LRIG1)	NP_001364278.1:p.Gly498Val
NM_015541.3:c.2777G>T (LRIG1) MANE Select	NP_056356.2:p.Gly926Val