Canonical Allele Identifier: CA407828351

Gene: LILRA2 LILRA1

Linked Data

• MyVariant Identifiers: chr19:g.54587342G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54587342G>C , CM000681.2:g.54587342G>C	GRCh38
NC_000019.8:g.59790621G>C	NCBI36
NG_034038.1:g.19346G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391738.8:c.1448G>C (LILRA2) MANE Select	ENSP00000375618.3:p.Arg483Thr
ENST00000251376.7:c.1397G>C (LILRA2)	ENSP00000251376.3:p.Arg466Thr
ENST00000251377.7:c.1448G>C (LILRA2)	ENSP00000251377.3:p.Arg483Thr
ENST00000391737.3:c.1361G>C (LILRA2)	ENSP00000375617.1:p.Arg454Thr
ENST00000391738.7:c.1448G>C (LILRA2)	ENSP00000375618.3:p.Arg483Thr
ENST00000472992.1:c.439G>C (LILRA2)
ENST00000618665.4:c.71-7323G>C (LILRA1)	ENSP00000479482.1:n.71-7323G>C
ENST00000629481.1:c.608G>C (LILRA2)	ENSP00000486483.1:p.Arg203Thr
NM_001130917.2:c.1448G>C (LILRA2)	NP_001124389.2:p.Arg483Thr
NM_001290270.1:c.1361G>C (LILRA2)	NP_001277199.1:p.Arg454Thr
NM_001290271.1:c.*183G>C (LILRA2)	NP_001277200.1:n.*183G>C
NM_006866.3:c.1397G>C (LILRA2)	NP_006857.2:p.Arg466Thr
XM_006722986.1:c.*183G>C (LILRA2)	XP_006723049.1:n.*183G>C
XM_011526385.1:c.1448G>C (LILRA2)	XP_011524687.1:p.Arg483Thr
XM_011526386.1:c.*183G>C (LILRA2)	XP_011524688.1:n.*183G>C
XM_011526387.1:c.1361G>C (LILRA2)	XP_011524689.1:p.Arg454Thr
XM_011526389.1:c.*183G>C (LILRA2)	XP_011524691.1:n.*183G>C
XM_017026224.1:c.*183G>C (LILRA2)	XP_016881713.1:n.*183G>C
NM_001130917.3:c.1448G>C (LILRA2) MANE Select	NP_001124389.2:p.Arg483Thr
NM_001290271.2:c.*183G>C (LILRA2)	NP_001277200.1:n.*183G>C
NM_006866.4:c.1397G>C (LILRA2)	NP_006857.2:p.Arg466Thr