Canonical Allele Identifier: CA346668204

Gene: LRPPRC

Linked Data

• MyVariant Identifiers: chr2:g.44145236A>T (hg19) ; chr2:g.43918097A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918097A>T , CM000664.2:g.43918097A>T	GRCh38
NC_000002.11:g.44145236A>T , CM000664.1:g.44145236A>T	GRCh37
NC_000002.10:g.43998740A>T	NCBI36
NG_008247.1:g.82909T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681993.1:n.628T>A
ENST00000682295.1:c.303+159T>A	ENSP00000507499.1:n.303+159T>A
ENST00000682303.1:c.*2862T>A	ENSP00000508325.1:n.*2862T>A
ENST00000682308.1:c.3076T>A	ENSP00000507056.1:p.Ser1026Thr
ENST00000682480.1:c.3094T>A	ENSP00000508344.1:p.Ser1032Thr
ENST00000682546.1:c.3073T>A	ENSP00000508188.1:p.Ser1025Thr
ENST00000682585.1:c.3076T>A	ENSP00000506885.1:p.Ser1026Thr
ENST00000682595.1:n.3660T>A
ENST00000682607.1:c.1494T>A
ENST00000682779.1:c.3067T>A	ENSP00000507947.1:p.Ser1023Thr
ENST00000682845.1:n.2178T>A
ENST00000682885.1:c.3031T>A	ENSP00000508036.1:p.Ser1011Thr
ENST00000682933.1:n.3150T>A
ENST00000683072.1:n.3660T>A
ENST00000683080.1:n.695T>A
ENST00000683125.1:c.3184T>A	ENSP00000507939.1:p.Ser1062Thr
ENST00000683213.1:c.3079T>A	ENSP00000507751.1:p.Ser1027Thr
ENST00000683220.1:c.3106T>A	ENSP00000507151.1:p.Ser1036Thr
ENST00000683329.1:n.3879T>A
ENST00000683346.1:c.*2951T>A	ENSP00000507458.1:n.*2951T>A
ENST00000683409.1:n.1683T>A
ENST00000683459.1:n.3663T>A
ENST00000683590.1:c.2897-5539T>A	ENSP00000506820.1:n.2897-5539T>A
ENST00000683623.1:c.2983T>A	ENSP00000507702.1:p.Ser995Thr
ENST00000683645.1:n.3627T>A
ENST00000683796.1:c.*2948T>A	ENSP00000508221.1:n.*2948T>A
ENST00000683802.1:n.6001T>A
ENST00000683833.1:c.3067T>A	ENSP00000506852.1:p.Ser1023Thr
ENST00000683994.1:c.3076T>A	ENSP00000507181.1:p.Ser1026Thr
ENST00000684290.1:c.*612T>A	ENSP00000507243.1:n.*612T>A
ENST00000684306.1:c.*2989T>A	ENSP00000508384.1:n.*2989T>A
ENST00000684341.1:n.3096T>A
ENST00000684383.1:c.*2714T>A	ENSP00000506863.1:n.*2714T>A
ENST00000684619.1:c.*2948T>A	ENSP00000508088.1:n.*2948T>A
ENST00000684705.1:n.197T>A
ENST00000684743.1:n.4107T>A
ENST00000260665.12:c.3076T>A MANE Select	ENSP00000260665.7:p.Ser1026Thr
ENST00000260665.11:c.3076T>A	ENSP00000260665.7:p.Ser1026Thr
NM_133259.3:c.3076T>A	NP_573566.2:p.Ser1026Thr
XM_006711915.2:c.2998T>A	XP_006711978.1:p.Ser1000Thr
XM_006711916.2:c.3076T>A	XP_006711979.1:p.Ser1026Thr
XM_011532473.1:c.3076T>A	XP_011530775.1:p.Ser1026Thr
XM_011532474.1:c.3076T>A	XP_011530776.1:p.Ser1026Thr
XM_006711916.3:c.3076T>A	XP_006711979.1:p.Ser1026Thr
XM_017003117.1:c.2998T>A	XP_016858606.1:p.Ser1000Thr
XR_002958896.1:n.3118T>A
NM_133259.4:c.3076T>A MANE Select	NP_573566.2:p.Ser1026Thr