Canonical Allele Identifier: CA997192467

Gene: LILRB1

Linked Data

• gnomAD v3: 19-54636698-CACGTT-C
• gnomAD v4: 19-54636698-CACGTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.54636699_54636703del , CM000681.2:g.54636699_54636703del	GRCh38
NC_000019.8:g.59839962_59839966del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000324602.12:c.1813-33_1813-29del MANE Select	ENSP00000315997.7:n.1813-33_1813-29del
ENST00000324602.11:c.1813-33_1813-29del	ENSP00000315997.7:n.1813-33_1813-29del
ENST00000396315.5:c.1813-33_1813-29del	ENSP00000379608.1:n.1813-33_1813-29del
ENST00000396317.5:c.1759-33_1759-29del	ENSP00000379610.1:n.1759-33_1759-29del
ENST00000396327.7:c.1810-33_1810-29del	ENSP00000379618.3:n.1810-33_1810-29del
ENST00000396331.5:c.1807-33_1807-29del	ENSP00000379622.1:n.1807-33_1807-29del
ENST00000396332.8:c.1810-33_1810-29del	ENSP00000379623.4:n.1810-33_1810-29del
ENST00000421584.5:c.1731-33_1731-29del	ENSP00000410165.1:n.1731-33_1731-29del
ENST00000427581.6:c.1960-33_1960-29del	ENSP00000395004.2:n.1960-33_1960-29del
ENST00000462628.5:n.1591-33_1591-29del
NM_001081637.2:c.1813-33_1813-29del	NP_001075106.2:n.1813-33_1813-29del
NM_001081638.3:c.1810-33_1810-29del	NP_001075107.2:n.1810-33_1810-29del
NM_001081639.3:c.1810-33_1810-29del	NP_001075108.2:n.1810-33_1810-29del
NM_001278398.2:c.1759-33_1759-29del	NP_001265327.2:n.1759-33_1759-29del
NM_006669.6:c.1807-33_1807-29del	NP_006660.4:n.1807-33_1807-29del
NR_103518.2:n.1896-33_1896-29del
XM_011526331.1:c.1843-33_1843-29del	XP_011524633.1:n.1843-33_1843-29del
XM_011526332.1:c.1840-33_1840-29del	XP_011524634.1:n.1840-33_1840-29del
XM_011526333.1:c.1840-33_1840-29del	XP_011524635.1:n.1840-33_1840-29del
XM_011526334.1:c.1864-33_1864-29del	XP_011524636.1:n.1864-33_1864-29del
XM_011526335.1:c.1684-33_1684-29del	XP_011524637.1:n.1684-33_1684-29del
XM_011526336.1:c.1651-33_1651-29del	XP_011524638.1:n.1651-33_1651-29del
XM_011526339.1:c.1807-33_1807-29del	XP_011524641.1:n.1807-33_1807-29del
XM_011526331.2:c.1843-33_1843-29del	XP_011524633.1:n.1843-33_1843-29del
XM_011526332.3:c.1840-33_1840-29del	XP_011524634.1:n.1840-33_1840-29del
XM_011526335.2:c.1684-33_1684-29del	XP_011524637.1:n.1684-33_1684-29del
XM_011526336.2:c.1651-33_1651-29del	XP_011524638.1:n.1651-33_1651-29del
XM_017026182.2:c.1840-33_1840-29del	XP_016881671.1:n.1840-33_1840-29del
XM_017026183.2:c.1837-33_1837-29del	XP_016881672.1:n.1837-33_1837-29del
XM_017026184.2:c.1837-33_1837-29del	XP_016881673.1:n.1837-33_1837-29del
XM_017026185.1:c.1807-33_1807-29del	XP_016881674.1:n.1807-33_1807-29del
XM_017026186.1:c.1864-33_1864-29del	XP_016881675.1:n.1864-33_1864-29del
XM_017026187.1:c.1864-33_1864-29del	XP_016881676.1:n.1864-33_1864-29del
XM_017026188.1:c.1861-33_1861-29del	XP_016881677.1:n.1861-33_1861-29del
XM_017026189.1:c.1861-33_1861-29del	XP_016881678.1:n.1861-33_1861-29del
XM_017026190.1:c.1858-33_1858-29del	XP_016881679.1:n.1858-33_1858-29del
XM_017026191.1:c.1654-33_1654-29del	XP_016881680.1:n.1654-33_1654-29del
XR_001753590.2:n.2060-33_2060-29del
XR_001753591.1:n.2065-33_2065-29del
XR_002958244.1:n.2057-33_2057-29del
NM_001081637.3:c.1813-33_1813-29del MANE Select	NP_001075106.2:n.1813-33_1813-29del
NM_001081638.4:c.1810-33_1810-29del	NP_001075107.2:n.1810-33_1810-29del
NM_001081639.4:c.1810-33_1810-29del	NP_001075108.2:n.1810-33_1810-29del
NM_001388355.1:c.1810-33_1810-29del	NP_001375284.1:n.1810-33_1810-29del
NM_001388356.1:c.1810-33_1810-29del	NP_001375285.1:n.1810-33_1810-29del
NM_001388357.1:c.1810-33_1810-29del	NP_001375286.1:n.1810-33_1810-29del
NM_001388358.1:c.1813-33_1813-29del	NP_001375287.1:n.1813-33_1813-29del
NM_006669.7:c.1807-33_1807-29del	NP_006660.4:n.1807-33_1807-29del