Canonical Allele Identifier: CA2494002042

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43944013A= , CM000664.2:g.43944013A=	GRCh38
NC_000002.11:g.44171152A= , CM000664.1:g.44171152A=	GRCh37
NC_000002.10:g.44024656A=	NCBI36
NG_008247.1:g.56993T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.2297-119T=	ENSP00000386562.2:n.2297-119T=
ENST00000447246.2:c.2297-119T=	ENSP00000403637.2:n.2297-119T=
ENST00000681961.1:n.2317-119T=
ENST00000682104.1:c.2171-119T=	ENSP00000507716.1:n.2171-119T=
ENST00000682303.1:c.*2083-119T=	ENSP00000508325.1:n.*2083-119T=
ENST00000682308.1:c.2297-119T=	ENSP00000507056.1:n.2297-119T=
ENST00000682480.1:c.2297-119T=	ENSP00000508344.1:n.2297-119T=
ENST00000682546.1:c.2294-119T=	ENSP00000508188.1:n.2294-119T=
ENST00000682585.1:c.2297-119T=	ENSP00000506885.1:n.2297-119T=
ENST00000682595.1:n.2879-119T=
ENST00000682607.1:c.715-119T=
ENST00000682779.1:c.2288-119T=	ENSP00000507947.1:n.2288-119T=
ENST00000682845.1:n.1280T=
ENST00000682885.1:c.2252-119T=	ENSP00000508036.1:n.2252-119T=
ENST00000682933.1:n.2371-119T=
ENST00000683072.1:n.2879-119T=
ENST00000683125.1:c.2297-119T=	ENSP00000507939.1:n.2297-119T=
ENST00000683213.1:c.2300-119T=	ENSP00000507751.1:n.2300-119T=
ENST00000683220.1:c.2327-119T=	ENSP00000507151.1:n.2327-119T=
ENST00000683329.1:n.3100-119T=
ENST00000683346.1:c.*2172-119T=	ENSP00000507458.1:n.*2172-119T=
ENST00000683459.1:n.2884-119T=
ENST00000683590.1:c.2297-119T=	ENSP00000506820.1:n.2297-119T=
ENST00000683623.1:c.2297-212T=	ENSP00000507702.1:n.2297-212T=
ENST00000683645.1:n.2848-119T=
ENST00000683694.1:n.1048-119T=
ENST00000683796.1:c.*2169-119T=	ENSP00000508221.1:n.*2169-119T=
ENST00000683802.1:n.5222-119T=
ENST00000683833.1:c.2288-119T=	ENSP00000506852.1:n.2288-119T=
ENST00000683989.1:c.2297-119T=	ENSP00000507510.1:n.2297-119T=
ENST00000683994.1:c.2297-119T=	ENSP00000507181.1:n.2297-119T=
ENST00000684290.1:c.2211-119T=	ENSP00000507243.1:n.2211-119T=
ENST00000684306.1:c.*2210-119T=	ENSP00000508384.1:n.*2210-119T=
ENST00000684341.1:n.2317-119T=
ENST00000684383.1:c.*1935-119T=	ENSP00000506863.1:n.*1935-119T=
ENST00000684619.1:c.*2169-119T=	ENSP00000508088.1:n.*2169-119T=
ENST00000684743.1:n.3328-119T=
ENST00000260665.12:c.2297-119T= MANE Select	ENSP00000260665.7:n.2297-119T=
ENST00000260665.11:c.2297-119T=	ENSP00000260665.7:n.2297-119T=
NM_133259.3:c.2297-119T=	NP_573566.2:n.2297-119T=
XM_006711915.2:c.2219-119T=	XP_006711978.1:n.2219-119T=
XM_006711916.2:c.2297-119T=	XP_006711979.1:n.2297-119T=
XM_011532473.1:c.2297-119T=	XP_011530775.1:n.2297-119T=
XM_011532474.1:c.2297-119T=	XP_011530776.1:n.2297-119T=
XM_006711916.3:c.2297-119T=	XP_006711979.1:n.2297-119T=
XM_017003117.1:c.2219-119T=	XP_016858606.1:n.2219-119T=
XR_002958896.1:n.2339-119T=
NM_133259.4:c.2297-119T= MANE Select	NP_573566.2:n.2297-119T=