Canonical Allele Identifier: CA2148330052
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77286744T= , CM000676.2:g.77286744T= GRCh38
NC_000014.8:g.77753087T= , CM000676.1:g.77753087T= GRCh37
NC_000014.7:g.76822840T= NCBI36
NG_008897.1:g.39139A= , LRG_844:g.39139A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556394.2:c.873A= ENSP00000451967.2:p.Ile291=
ENST00000682247.1:c.1332A= ENSP00000507213.1:p.Ile444=
ENST00000682382.1:c.904A=
ENST00000682395.1:n.1510A=
ENST00000682459.1:n.1035A=
ENST00000682467.1:c.1332A= ENSP00000508062.1:p.Ile444=
ENST00000682706.1:n.109A=
ENST00000682795.1:c.1332A= ENSP00000507574.1:p.Ile444=
ENST00000682895.1:n.1048A=
ENST00000682955.1:n.620A=
ENST00000683188.1:c.1307A=
ENST00000683328.1:c.325A= ENSP00000508096.1:n.325A=
ENST00000683380.1:n.996A=
ENST00000683828.1:c.1041A=
ENST00000684259.1:n.1183A=
ENST00000684444.1:c.79A=
ENST00000684549.1:n.883A=
ENST00000261534.9:c.1332A= MANE Select ENSP00000261534.4:p.Ile444=
ENST00000261534.8:c.1332A= ENSP00000261534.4:p.Ile444=
ENST00000452340.7:n.1355A=
ENST00000553880.5:n.203A=
ENST00000554767.5:n.2118A=
ENST00000554884.5:n.324A=
ENST00000556404.1:n.466A=
ENST00000557675.5:n.422A=
NM_013382.5:c.1332A= , LRG_844t1:c.1332A= NP_037514.2:p.Ile444=
XM_011536675.1:c.1332A= XP_011534977.1:p.Ile444=
XM_011536676.1:c.999A= XP_011534978.1:p.Ile333=
XM_011536677.1:c.873A= XP_011534979.1:p.Ile291=
XM_011536678.1:c.1332A= XP_011534980.1:p.Ile444=
XM_011536679.1:c.426A= XP_011534981.1:p.Ile142=
XR_943416.1:n.1535A=
XM_011536675.2:c.1332A= XP_011534977.1:p.Ile444=
XM_011536676.2:c.999A= XP_011534978.1:p.Ile333=
XM_011536677.3:c.873A= XP_011534979.1:p.Ile291=
XR_001750279.1:n.1532A=
XR_001750282.1:n.1985A=
XR_943416.3:n.1533A=
NM_013382.6:c.1332A= NP_037514.2:p.Ile444=
NM_013382.7:c.1332A= MANE Select NP_037514.2:p.Ile444=