Canonical Allele Identifier: CA407828024

Gene: LILRA2 LILRA1

Linked Data

• MyVariant Identifiers: chr19:g.54587290C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54587290C>A , CM000681.2:g.54587290C>A	GRCh38
NC_000019.8:g.59790569C>A	NCBI36
NG_034038.1:g.19294C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391738.8:c.1396C>A (LILRA2) MANE Select	ENSP00000375618.3:p.Leu466Met
ENST00000251376.7:c.1345C>A (LILRA2)	ENSP00000251376.3:p.Leu449Met
ENST00000251377.7:c.1396C>A (LILRA2)	ENSP00000251377.3:p.Leu466Met
ENST00000391737.3:c.1309C>A (LILRA2)	ENSP00000375617.1:p.Leu437Met
ENST00000391738.7:c.1396C>A (LILRA2)	ENSP00000375618.3:p.Leu466Met
ENST00000472992.1:c.387C>A (LILRA2)
ENST00000618665.4:c.71-7375C>A (LILRA1)	ENSP00000479482.1:n.71-7375C>A
ENST00000629481.1:c.556C>A (LILRA2)	ENSP00000486483.1:p.Leu186Met
NM_001130917.2:c.1396C>A (LILRA2)	NP_001124389.2:p.Leu466Met
NM_001290270.1:c.1309C>A (LILRA2)	NP_001277199.1:p.Leu437Met
NM_001290271.1:c.*131C>A (LILRA2)	NP_001277200.1:n.*131C>A
NM_006866.3:c.1345C>A (LILRA2)	NP_006857.2:p.Leu449Met
XM_006722986.1:c.*131C>A (LILRA2)	XP_006723049.1:n.*131C>A
XM_011526385.1:c.1396C>A (LILRA2)	XP_011524687.1:p.Leu466Met
XM_011526386.1:c.*131C>A (LILRA2)	XP_011524688.1:n.*131C>A
XM_011526387.1:c.1309C>A (LILRA2)	XP_011524689.1:p.Leu437Met
XM_011526389.1:c.*131C>A (LILRA2)	XP_011524691.1:n.*131C>A
XM_017026224.1:c.*131C>A (LILRA2)	XP_016881713.1:n.*131C>A
NM_001130917.3:c.1396C>A (LILRA2) MANE Select	NP_001124389.2:p.Leu466Met
NM_001290271.2:c.*131C>A (LILRA2)	NP_001277200.1:n.*131C>A
NM_006866.4:c.1345C>A (LILRA2)	NP_006857.2:p.Leu449Met