Canonical Allele Identifier: CA1048997448

Gene: SLC25A26 LRIG1

Linked Data

• dbSNP Id: rs2242285
• gnomAD v3: 3-66381178-A-T
• gnomAD v4: 3-66381178-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.66381178A>T , CM000665.2:g.66381178A>T	GRCh38
NC_000003.11:g.66431602A>T , CM000665.1:g.66431602A>T	GRCh37
NC_000003.10:g.66514292A>T	NCBI36
NG_054637.1:g.252569A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691461.1:c.*1143+225A>T (SLC25A26)	ENSP00000510022.1:n.*1143+225A>T
ENST00000273261.8:c.2770+301T>A (LRIG1) MANE Select	ENSP00000273261.3:n.2770+301T>A
ENST00000273261.7:c.2770+301T>A (LRIG1)	ENSP00000273261.3:n.2770+301T>A
ENST00000383703.3:c.2701+301T>A (LRIG1)	ENSP00000373208.3:n.2701+301T>A
ENST00000464350.6:c.*1547+225A>T (SLC25A26)	ENSP00000432574.2:n.*1547+225A>T
ENST00000495037.1:n.1786+301T>A (LRIG1)
ENST00000496559.6:n.2152+301T>A (LRIG1)
NM_015541.2:c.2770+301T>A (LRIG1)	NP_056356.2:n.2770+301T>A
XM_011533578.1:c.2626+301T>A (LRIG1)	XP_011531880.1:n.2626+301T>A
XM_011533579.1:c.1990+301T>A (LRIG1)	XP_011531881.1:n.1990+301T>A
XM_011533578.2:c.2626+301T>A (LRIG1)	XP_011531880.1:n.2626+301T>A
XM_011533579.3:c.1990+301T>A (LRIG1)	XP_011531881.1:n.1990+301T>A
XM_017006134.2:c.2695+301T>A (LRIG1)	XP_016861623.1:n.2695+301T>A
XM_017006135.1:c.2092+301T>A (LRIG1)	XP_016861624.1:n.2092+301T>A
XM_017006136.2:c.1990+301T>A (LRIG1)	XP_016861625.1:n.1990+301T>A
NM_001377344.1:c.2695+301T>A (LRIG1)	NP_001364273.1:n.2695+301T>A
NM_001377345.1:c.1990+301T>A (LRIG1)	NP_001364274.1:n.1990+301T>A
NM_001377346.1:c.1990+301T>A (LRIG1)	NP_001364275.1:n.1990+301T>A
NM_001377347.1:c.1768+301T>A (LRIG1)	NP_001364276.1:n.1768+301T>A
NM_001377348.1:c.1741+301T>A (LRIG1)	NP_001364277.1:n.1741+301T>A
NM_001377349.1:c.1486+301T>A (LRIG1)	NP_001364278.1:n.1486+301T>A
NM_015541.3:c.2770+301T>A (LRIG1) MANE Select	NP_056356.2:n.2770+301T>A