Canonical Allele Identifier: CA407824375

Gene: LAIR1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54364315T>C , CM000681.2:g.54364315T>C	GRCh38
NC_000019.8:g.59567734T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002287.6:c.50A>G MANE Select	NP_002278.2:p.Gln17Arg
ENST00000391742.7:c.50A>G MANE Select	ENSP00000375622.2:p.Gln17Arg
NM_001289023.2:c.50A>G	NP_001275952.2:p.Gln17Arg
NM_001289023.3:c.50A>G	NP_001275952.2:p.Gln17Arg
NM_001289025.2:c.50A>G	NP_001275954.2:p.Gln17Arg
NM_001289025.3:c.50A>G	NP_001275954.2:p.Gln17Arg
NM_001289026.2:c.32A>G	NP_001275955.2:p.Gln11Arg
NM_001289026.3:c.32A>G	NP_001275955.2:p.Gln11Arg
NM_001289027.2:c.17-3106A>G	NP_001275956.2:n.17-3106A>G
NM_001289027.3:c.17-3106A>G	NP_001275956.2:n.17-3106A>G
NM_002287.5:c.50A>G	NP_002278.2:p.Gln17Arg
NM_021706.4:c.50A>G	NP_068352.2:p.Gln17Arg
NM_021706.5:c.50A>G	NP_068352.2:p.Gln17Arg
NR_110279.2:n.360A>G
NR_110279.3:n.177A>G
NR_110280.2:n.516A>G
NR_110280.3:n.333A>G
ENST00000348231.8:c.50A>G	ENSP00000301193.4:p.Gln17Arg
ENST00000391741.6:c.50A>G	ENSP00000375621.2:p.Gln17Arg
ENST00000391742.6:c.50A>G	ENSP00000375622.2:p.Gln17Arg
ENST00000391743.7:c.17-3106A>G	ENSP00000375623.3:n.17-3106A>G
ENST00000418556.5:c.50A>G	ENSP00000412796.1:p.Gln17Arg
ENST00000420483.5:c.50A>G	ENSP00000399710.1:p.Gln17Arg
ENST00000423853.5:n.516A>G
ENST00000427131.2:n.333A>G
ENST00000434277.6:c.50A>G	ENSP00000391003.2:p.Gln17Arg
ENST00000436513.5:c.50A>G	ENSP00000411632.1:p.Gln17Arg
ENST00000438193.1:c.32A>G	ENSP00000392058.1:p.Gln11Arg
ENST00000440716.5:n.238A>G
ENST00000463489.5:n.77A>G
ENST00000467269.5:n.53A>G
ENST00000468656.5:n.86A>G
ENST00000474878.5:c.50A>G	ENSP00000418998.1:p.Gln17Arg
ENST00000480122.1:n.304A>G
ENST00000484116.5:n.95A>G
XM_011526960.1:c.50A>G	XP_011525262.1:p.Gln17Arg
XM_017026803.2:c.50A>G	XP_016882292.1:p.Gln17Arg