Canonical Allele Identifier: CA2148315310
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278749A= , CM000676.2:g.77278749A= GRCh38
NC_000014.8:g.77745092A= , CM000676.1:g.77745092A= GRCh37
NC_000014.7:g.76814845A= NCBI36
NG_008897.1:g.47134T= , LRG_844:g.47134T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.937T=
ENST00000556394.2:c.1553T= ENSP00000451967.2:p.Leu518=
ENST00000682128.1:c.313T= ENSP00000506976.1:n.313T=
ENST00000682247.1:c.2001T= ENSP00000507213.1:p.Ala667=
ENST00000682395.1:n.2476T=
ENST00000682459.1:n.1715T=
ENST00000682467.1:c.1892-241T= ENSP00000508062.1:n.1892-241T=
ENST00000682615.1:n.366T=
ENST00000682795.1:c.2159T= ENSP00000507574.1:p.Leu720=
ENST00000682895.1:n.1728T=
ENST00000682955.1:n.1586T=
ENST00000683095.1:c.418T= ENSP00000508040.1:n.418T=
ENST00000683188.1:c.2273T=
ENST00000683380.1:n.1676T=
ENST00000683907.1:c.277T= ENSP00000507754.1:n.277T=
ENST00000684172.1:c.388T= ENSP00000508391.1:n.388T=
ENST00000684259.1:n.3779T=
ENST00000684538.1:n.1391T=
ENST00000684549.1:n.1563T=
ENST00000261534.9:c.2012T= MANE Select ENSP00000261534.4:p.Leu671=
ENST00000261534.8:c.2012T= ENSP00000261534.4:p.Leu671=
ENST00000452340.7:n.2988T=
ENST00000554767.5:n.2798T=
ENST00000555710.1:c.373T= ENSP00000451730.1:n.373T=
ENST00000556394.1:c.88-241T=
ENST00000556446.1:n.313T=
ENST00000602717.5:c.227T= ENSP00000487704.1:p.Leu76=
NM_013382.5:c.2012T= , LRG_844t1:c.2012T= NP_037514.2:p.Leu671=
XM_011536675.1:c.2201T= XP_011534977.1:p.Leu734=
XM_011536676.1:c.1868T= XP_011534978.1:p.Leu623=
XM_011536677.1:c.1742T= XP_011534979.1:p.Leu581=
XM_011536679.1:c.1295T= XP_011534981.1:p.Leu432=
XR_943416.1:n.2265T=
XM_011536675.2:c.2201T= XP_011534977.1:p.Leu734=
XM_011536676.2:c.1868T= XP_011534978.1:p.Leu623=
XM_011536677.3:c.1742T= XP_011534979.1:p.Leu581=
XR_001750279.1:n.2298T=
XR_001750282.1:n.2951T=
XR_943416.3:n.2263T=
NM_013382.6:c.2012T= NP_037514.2:p.Leu671=
NM_013382.7:c.2012T= MANE Select NP_037514.2:p.Leu671=