Canonical Allele Identifier: CA6406442

Gene: LTBR

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6384647G>A , CM000674.2:g.6384647G>A	GRCh38
NC_000012.11:g.6493813G>A , CM000674.1:g.6493813G>A	GRCh37
NC_000012.10:g.6364074G>A	NCBI36
NG_033039.1:g.14280G>A
NG_033039.2:g.14280G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228918.9:c.156G>A MANE Select	ENSP00000228918.4:p.Glu52=
ENST00000228918.8:c.156G>A	ENSP00000228918.4:p.Glu52=
ENST00000535739.5:n.339G>A
ENST00000536876.5:c.156G>A	ENSP00000437647.1:p.Glu52=
ENST00000539925.5:c.99G>A	ENSP00000440875.1:p.Glu33=
ENST00000542830.5:n.325G>A
ENST00000543190.5:c.-166G>A	ENSP00000438955.1:n.-166G>A
ENST00000546296.5:n.610G>A
NM_001270987.1:c.99G>A	NP_001257916.1:p.Glu33=
NM_002342.2:c.156G>A	NP_002333.1:p.Glu52=
XM_005253688.1:c.156G>A	XP_005253745.1:p.Glu52=
XM_006718983.2:c.156G>A	XP_006719046.1:p.Glu52=
XM_005253688.2:c.156G>A	XP_005253745.1:p.Glu52=
XM_006718983.3:c.156G>A	XP_006719046.1:p.Glu52=
NM_002342.3:c.156G>A MANE Select	NP_002333.1:p.Glu52=
NM_001270987.2:c.99G>A	NP_001257916.1:p.Glu33=