Canonical Allele Identifier: CA2587150778

Gene: LILRB1

Linked Data

• gnomAD v4: 19-54636692-CCCCACCACGTTCCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54636696_54636710del , CM000681.2:g.54636696_54636710del	GRCh38
NC_000019.8:g.59839959_59839973del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000324602.12:c.1813-36_1813-22del MANE Select	ENSP00000315997.7:n.1813-36_1813-22del
ENST00000324602.11:c.1813-36_1813-22del	ENSP00000315997.7:n.1813-36_1813-22del
ENST00000396315.5:c.1813-36_1813-22del	ENSP00000379608.1:n.1813-36_1813-22del
ENST00000396317.5:c.1759-36_1759-22del	ENSP00000379610.1:n.1759-36_1759-22del
ENST00000396327.7:c.1810-36_1810-22del	ENSP00000379618.3:n.1810-36_1810-22del
ENST00000396331.5:c.1807-36_1807-22del	ENSP00000379622.1:n.1807-36_1807-22del
ENST00000396332.8:c.1810-36_1810-22del	ENSP00000379623.4:n.1810-36_1810-22del
ENST00000421584.5:c.1731-36_1731-22del	ENSP00000410165.1:n.1731-36_1731-22del
ENST00000427581.6:c.1960-36_1960-22del	ENSP00000395004.2:n.1960-36_1960-22del
ENST00000462628.5:n.1591-36_1591-22del
NM_001081637.2:c.1813-36_1813-22del	NP_001075106.2:n.1813-36_1813-22del
NM_001081638.3:c.1810-36_1810-22del	NP_001075107.2:n.1810-36_1810-22del
NM_001081639.3:c.1810-36_1810-22del	NP_001075108.2:n.1810-36_1810-22del
NM_001278398.2:c.1759-36_1759-22del	NP_001265327.2:n.1759-36_1759-22del
NM_006669.6:c.1807-36_1807-22del	NP_006660.4:n.1807-36_1807-22del
NR_103518.2:n.1896-36_1896-22del
XM_011526331.1:c.1843-36_1843-22del	XP_011524633.1:n.1843-36_1843-22del
XM_011526332.1:c.1840-36_1840-22del	XP_011524634.1:n.1840-36_1840-22del
XM_011526333.1:c.1840-36_1840-22del	XP_011524635.1:n.1840-36_1840-22del
XM_011526334.1:c.1864-36_1864-22del	XP_011524636.1:n.1864-36_1864-22del
XM_011526335.1:c.1684-36_1684-22del	XP_011524637.1:n.1684-36_1684-22del
XM_011526336.1:c.1651-36_1651-22del	XP_011524638.1:n.1651-36_1651-22del
XM_011526339.1:c.1807-36_1807-22del	XP_011524641.1:n.1807-36_1807-22del
XM_011526331.2:c.1843-36_1843-22del	XP_011524633.1:n.1843-36_1843-22del
XM_011526332.3:c.1840-36_1840-22del	XP_011524634.1:n.1840-36_1840-22del
XM_011526335.2:c.1684-36_1684-22del	XP_011524637.1:n.1684-36_1684-22del
XM_011526336.2:c.1651-36_1651-22del	XP_011524638.1:n.1651-36_1651-22del
XM_017026182.2:c.1840-36_1840-22del	XP_016881671.1:n.1840-36_1840-22del
XM_017026183.2:c.1837-36_1837-22del	XP_016881672.1:n.1837-36_1837-22del
XM_017026184.2:c.1837-36_1837-22del	XP_016881673.1:n.1837-36_1837-22del
XM_017026185.1:c.1807-36_1807-22del	XP_016881674.1:n.1807-36_1807-22del
XM_017026186.1:c.1864-36_1864-22del	XP_016881675.1:n.1864-36_1864-22del
XM_017026187.1:c.1864-36_1864-22del	XP_016881676.1:n.1864-36_1864-22del
XM_017026188.1:c.1861-36_1861-22del	XP_016881677.1:n.1861-36_1861-22del
XM_017026189.1:c.1861-36_1861-22del	XP_016881678.1:n.1861-36_1861-22del
XM_017026190.1:c.1858-36_1858-22del	XP_016881679.1:n.1858-36_1858-22del
XM_017026191.1:c.1654-36_1654-22del	XP_016881680.1:n.1654-36_1654-22del
XR_001753590.2:n.2060-36_2060-22del
XR_001753591.1:n.2065-36_2065-22del
XR_002958244.1:n.2057-36_2057-22del
NM_001081637.3:c.1813-36_1813-22del MANE Select	NP_001075106.2:n.1813-36_1813-22del
NM_001081638.4:c.1810-36_1810-22del	NP_001075107.2:n.1810-36_1810-22del
NM_001081639.4:c.1810-36_1810-22del	NP_001075108.2:n.1810-36_1810-22del
NM_001388355.1:c.1810-36_1810-22del	NP_001375284.1:n.1810-36_1810-22del
NM_001388356.1:c.1810-36_1810-22del	NP_001375285.1:n.1810-36_1810-22del
NM_001388357.1:c.1810-36_1810-22del	NP_001375286.1:n.1810-36_1810-22del
NM_001388358.1:c.1813-36_1813-22del	NP_001375287.1:n.1813-36_1813-22del
NM_006669.7:c.1807-36_1807-22del	NP_006660.4:n.1807-36_1807-22del