Canonical Allele Identifier: CA769066409

Gene: LRPPRC

Linked Data

• dbSNP Id: rs1294203291
• MyVariant Identifiers: chr2:g.44171192A>G (hg19) ; chr2:g.43944053A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43944053A>G , CM000664.2:g.43944053A>G	GRCh38
NC_000002.11:g.44171192A>G , CM000664.1:g.44171192A>G	GRCh37
NC_000002.10:g.44024696A>G	NCBI36
NG_008247.1:g.56953T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409659.6:c.2297-159T>C	ENSP00000386562.2:n.2297-159T>C
ENST00000447246.2:c.2297-159T>C	ENSP00000403637.2:n.2297-159T>C
ENST00000681961.1:n.2317-159T>C
ENST00000682104.1:c.2171-159T>C	ENSP00000507716.1:n.2171-159T>C
ENST00000682303.1:c.*2083-159T>C	ENSP00000508325.1:n.*2083-159T>C
ENST00000682308.1:c.2297-159T>C	ENSP00000507056.1:n.2297-159T>C
ENST00000682480.1:c.2297-159T>C	ENSP00000508344.1:n.2297-159T>C
ENST00000682546.1:c.2294-159T>C	ENSP00000508188.1:n.2294-159T>C
ENST00000682585.1:c.2297-159T>C	ENSP00000506885.1:n.2297-159T>C
ENST00000682595.1:n.2879-159T>C
ENST00000682607.1:c.715-159T>C
ENST00000682779.1:c.2288-159T>C	ENSP00000507947.1:n.2288-159T>C
ENST00000682845.1:n.1240T>C
ENST00000682885.1:c.2252-159T>C	ENSP00000508036.1:n.2252-159T>C
ENST00000682933.1:n.2371-159T>C
ENST00000683072.1:n.2879-159T>C
ENST00000683125.1:c.2297-159T>C	ENSP00000507939.1:n.2297-159T>C
ENST00000683213.1:c.2300-159T>C	ENSP00000507751.1:n.2300-159T>C
ENST00000683220.1:c.2327-159T>C	ENSP00000507151.1:n.2327-159T>C
ENST00000683329.1:n.3100-159T>C
ENST00000683346.1:c.*2172-159T>C	ENSP00000507458.1:n.*2172-159T>C
ENST00000683459.1:n.2884-159T>C
ENST00000683590.1:c.2297-159T>C	ENSP00000506820.1:n.2297-159T>C
ENST00000683623.1:c.2297-252T>C	ENSP00000507702.1:n.2297-252T>C
ENST00000683645.1:n.2848-159T>C
ENST00000683694.1:n.1048-159T>C
ENST00000683796.1:c.*2169-159T>C	ENSP00000508221.1:n.*2169-159T>C
ENST00000683802.1:n.5222-159T>C
ENST00000683833.1:c.2288-159T>C	ENSP00000506852.1:n.2288-159T>C
ENST00000683989.1:c.2297-159T>C	ENSP00000507510.1:n.2297-159T>C
ENST00000683994.1:c.2297-159T>C	ENSP00000507181.1:n.2297-159T>C
ENST00000684290.1:c.2211-159T>C	ENSP00000507243.1:n.2211-159T>C
ENST00000684306.1:c.*2210-159T>C	ENSP00000508384.1:n.*2210-159T>C
ENST00000684341.1:n.2317-159T>C
ENST00000684383.1:c.*1935-159T>C	ENSP00000506863.1:n.*1935-159T>C
ENST00000684619.1:c.*2169-159T>C	ENSP00000508088.1:n.*2169-159T>C
ENST00000684743.1:n.3328-159T>C
ENST00000260665.12:c.2297-159T>C MANE Select	ENSP00000260665.7:n.2297-159T>C
ENST00000260665.11:c.2297-159T>C	ENSP00000260665.7:n.2297-159T>C
NM_133259.3:c.2297-159T>C	NP_573566.2:n.2297-159T>C
XM_006711915.2:c.2219-159T>C	XP_006711978.1:n.2219-159T>C
XM_006711916.2:c.2297-159T>C	XP_006711979.1:n.2297-159T>C
XM_011532473.1:c.2297-159T>C	XP_011530775.1:n.2297-159T>C
XM_011532474.1:c.2297-159T>C	XP_011530776.1:n.2297-159T>C
XM_006711916.3:c.2297-159T>C	XP_006711979.1:n.2297-159T>C
XM_017003117.1:c.2219-159T>C	XP_016858606.1:n.2219-159T>C
XR_002958896.1:n.2339-159T>C
NM_133259.4:c.2297-159T>C MANE Select	NP_573566.2:n.2297-159T>C