Canonical Allele Identifier: CA2148315457
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278817T= , CM000676.2:g.77278817T= GRCh38
NC_000014.8:g.77745160T= , CM000676.1:g.77745160T= GRCh37
NC_000014.7:g.76814913T= NCBI36
NG_008897.1:g.47066A= , LRG_844:g.47066A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.869A=
ENST00000556394.2:c.1485A= ENSP00000451967.2:p.Thr495=
ENST00000682128.1:c.245A= ENSP00000506976.1:n.245A=
ENST00000682247.1:c.1933A= ENSP00000507213.1:p.Thr645=
ENST00000682395.1:n.2408A=
ENST00000682459.1:n.1647A=
ENST00000682467.1:c.1892-309A= ENSP00000508062.1:n.1892-309A=
ENST00000682615.1:n.298A=
ENST00000682795.1:c.2091A= ENSP00000507574.1:p.Thr697=
ENST00000682895.1:n.1660A=
ENST00000682955.1:n.1518A=
ENST00000683095.1:c.350A= ENSP00000508040.1:n.350A=
ENST00000683188.1:c.2205A=
ENST00000683380.1:n.1608A=
ENST00000683828.1:c.1653A=
ENST00000683907.1:c.209A= ENSP00000507754.1:p.His70=
ENST00000684172.1:c.320A= ENSP00000508391.1:n.320A=
ENST00000684259.1:n.3711A=
ENST00000684538.1:n.1323A=
ENST00000684549.1:n.1495A=
ENST00000261534.9:c.1944A= MANE Select ENSP00000261534.4:p.Thr648=
ENST00000261534.8:c.1944A= ENSP00000261534.4:p.Thr648=
ENST00000452340.7:n.2920A=
ENST00000554767.5:n.2730A=
ENST00000555134.1:n.869A=
ENST00000555710.1:c.305A= ENSP00000451730.1:n.305A=
ENST00000556171.1:c.536A=
ENST00000556394.1:c.88-309A=
ENST00000556446.1:n.245A=
ENST00000602717.5:c.159A= ENSP00000487704.1:p.Thr53=
NM_013382.5:c.1944A= , LRG_844t1:c.1944A= NP_037514.2:p.Thr648=
XM_011536675.1:c.2133A= XP_011534977.1:p.Thr711=
XM_011536676.1:c.1800A= XP_011534978.1:p.Thr600=
XM_011536677.1:c.1674A= XP_011534979.1:p.Thr558=
XM_011536679.1:c.1227A= XP_011534981.1:p.Thr409=
XR_943416.1:n.2197A=
XM_011536675.2:c.2133A= XP_011534977.1:p.Thr711=
XM_011536676.2:c.1800A= XP_011534978.1:p.Thr600=
XM_011536677.3:c.1674A= XP_011534979.1:p.Thr558=
XR_001750279.1:n.2230A=
XR_001750282.1:n.2883A=
XR_943416.3:n.2195A=
NM_013382.6:c.1944A= NP_037514.2:p.Thr648=
NM_013382.7:c.1944A= MANE Select NP_037514.2:p.Thr648=