Canonical Allele Identifier: CA390520977
Gene: POMT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77306366C>T , CM000676.2:g.77306366C>T GRCh38
NC_000014.8:g.77772709C>T , CM000676.1:g.77772709C>T GRCh37
NC_000014.7:g.76842462C>T NCBI36
NG_008897.1:g.19517G>A , LRG_844:g.19517G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555675.6:n.138G>A
ENST00000556394.2:c.249-1566G>A ENSP00000451967.2:n.249-1566G>A
ENST00000556880.6:n.342G>A
ENST00000682247.1:c.409G>A ENSP00000507213.1:p.Glu137Lys
ENST00000682382.1:c.357G>A
ENST00000682395.1:n.138G>A
ENST00000682459.1:n.102+36G>A
ENST00000682467.1:c.409G>A ENSP00000508062.1:p.Glu137Lys
ENST00000682795.1:c.409G>A ENSP00000507574.1:p.Glu137Lys
ENST00000682895.1:n.125G>A
ENST00000682955.1:n.102+36G>A
ENST00000683188.1:c.204G>A
ENST00000683380.1:n.102+36G>A
ENST00000683828.1:c.278G>A
ENST00000684066.1:n.104G>A
ENST00000684102.1:n.155G>A
ENST00000684259.1:n.260G>A
ENST00000684479.1:n.76G>A
ENST00000684549.1:n.138G>A
ENST00000684600.1:c.223G>A
ENST00000684670.1:n.76G>A
ENST00000684746.1:n.106G>A
ENST00000261534.9:c.409G>A MANE Select ENSP00000261534.4:p.Glu137Lys
ENST00000261534.8:c.409G>A ENSP00000261534.4:p.Glu137Lys
ENST00000452340.7:n.432G>A
ENST00000553863.5:n.102+36G>A
ENST00000554948.1:c.136G>A ENSP00000452060.1:p.Glu46Lys
ENST00000555675.5:n.125G>A
ENST00000555788.5:n.243G>A
ENST00000556326.5:c.*75G>A ENSP00000450630.1:n.*75G>A
ENST00000556880.5:n.342G>A
ENST00000557525.1:n.499G>A
NM_013382.5:c.409G>A , LRG_844t1:c.409G>A NP_037514.2:p.Glu137Lys
XM_011536675.1:c.409G>A XP_011534977.1:p.Glu137Lys
XM_011536676.1:c.76G>A XP_011534978.1:p.Glu26Lys
XM_011536677.1:c.409G>A XP_011534979.1:p.Glu137Lys
XM_011536678.1:c.409G>A XP_011534980.1:p.Glu137Lys
XM_011536680.1:c.409G>A XP_011534982.1:p.Glu137Lys
XR_943416.1:n.612G>A
XM_011536675.2:c.409G>A XP_011534977.1:p.Glu137Lys
XM_011536676.2:c.76G>A XP_011534978.1:p.Glu26Lys
XM_011536677.3:c.409G>A XP_011534979.1:p.Glu137Lys
XR_001750279.1:n.609G>A
XR_001750282.1:n.613G>A
XR_943416.3:n.610G>A
NM_013382.6:c.409G>A NP_037514.2:p.Glu137Lys
NM_013382.7:c.409G>A MANE Select NP_037514.2:p.Glu137Lys