Canonical Allele Identifier: CA3861905

Gene: MLIP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.54189888T>A , CM000668.2:g.54189888T>A	GRCh38
NC_000006.11:g.54054686T>A , CM000668.1:g.54054686T>A	GRCh37
NC_000006.10:g.54162645T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001281747.2:c.2563T>A MANE Select	NP_001268676.1:p.Ser855Thr
ENST00000502396.6:c.2563T>A MANE Select	ENSP00000426290.1:p.Ser855Thr
NM_001281746.1:c.2530T>A	NP_001268675.1:p.Ser844Thr
NM_001281746.2:c.2530T>A	NP_001268675.1:p.Ser844Thr
NM_001281747.1:c.2563T>A	NP_001268676.1:p.Ser855Thr
NM_138569.2:c.958T>A	NP_612636.2:p.Ser320Thr
NM_138569.3:c.958T>A	NP_612636.2:p.Ser320Thr
ENST00000274897.9:c.958T>A	ENSP00000274897.5:p.Ser320Thr
ENST00000370876.6:c.490T>A	ENSP00000359913.2:p.Ser164Thr
ENST00000370877.6:c.646T>A	ENSP00000359914.2:p.Ser216Thr
ENST00000447836.6:c.460T>A	ENSP00000411917.2:p.Ser154Thr
ENST00000502396.5:c.2563T>A	ENSP00000426290.1:p.Ser855Thr
ENST00000509997.5:c.520T>A	ENSP00000427584.1:p.Ser174Thr
ENST00000511744.1:n.2596T>A
ENST00000514433.1:c.745T>A	ENSP00000421444.1:p.Ser249Thr
ENST00000514921.5:c.2530T>A	ENSP00000425142.1:p.Ser844Thr
XM_005249476.3:c.2530T>A	XP_005249533.1:p.Ser844Thr
XM_005249476.5:c.2530T>A	XP_005249533.1:p.Ser844Thr
XM_005249477.3:c.2500T>A	XP_005249534.1:p.Ser834Thr
XM_005249478.3:c.2374T>A	XP_005249535.1:p.Ser792Thr
XM_005249478.5:c.2374T>A	XP_005249535.1:p.Ser792Thr
XM_005249480.3:c.958T>A	XP_005249537.1:p.Ser320Thr
XM_005249480.5:c.958T>A	XP_005249537.1:p.Ser320Thr
XM_006715245.2:c.2512T>A	XP_006715308.1:p.Ser838Thr
XM_006715245.3:c.2563T>A	XP_006715308.2:p.Ser855Thr
XM_006715247.2:c.2176T>A	XP_006715310.1:p.Ser726Thr
XM_006715248.2:c.2176T>A	XP_006715311.1:p.Ser726Thr
XM_011514990.1:c.2530T>A	XP_011513292.1:p.Ser844Thr
XM_017011465.1:c.2419T>A	XP_016866954.1:p.Ser807Thr
XM_017011466.2:c.2419T>A	XP_016866955.1:p.Ser807Thr
XM_017011467.1:c.2353T>A	XP_016866956.1:p.Ser785Thr
XM_017011468.1:c.2419T>A	XP_016866957.1:p.Ser807Thr
XM_017011469.1:c.2032T>A	XP_016866958.1:p.Ser678Thr
XM_017011470.1:c.784T>A	XP_016866959.1:p.Ser262Thr
XM_024446578.1:c.2176T>A	XP_024302346.1:p.Ser726Thr
XM_024446579.1:c.874T>A	XP_024302347.1:p.Ser292Thr
XM_024446580.1:c.814T>A	XP_024302348.1:p.Ser272Thr
XM_024446581.1:c.802T>A	XP_024302349.1:p.Ser268Thr
XM_024446582.1:c.676T>A	XP_024302350.1:p.Ser226Thr
XR_001744170.1:n.548+141A>T
XR_926891.1:n.404+141A>T