Canonical Allele Identifier: CA2148342387
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77301180G= , CM000676.2:g.77301180G= GRCh38
NC_000014.8:g.77767523G= , CM000676.1:g.77767523G= GRCh37
NC_000014.7:g.76837276G= NCBI36
NG_008897.1:g.24703C= , LRG_844:g.24703C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553863.6:c.179C= ENSP00000508202.1:n.179C=
ENST00000556394.2:c.358-1619C= ENSP00000451967.2:n.358-1619C=
ENST00000556880.6:n.750C=
ENST00000557289.2:c.70C=
ENST00000682247.1:c.726C= ENSP00000507213.1:p.Val242=
ENST00000682382.1:c.496-2409C=
ENST00000682395.1:n.455C=
ENST00000682459.1:n.390C=
ENST00000682467.1:c.726C= ENSP00000508062.1:p.Val242=
ENST00000682795.1:c.726C= ENSP00000507574.1:p.Val242=
ENST00000682895.1:n.442C=
ENST00000682955.1:n.212-2409C=
ENST00000683167.1:c.70C=
ENST00000683188.1:c.343-1619C=
ENST00000683300.1:c.109+3512C= ENSP00000507630.1:n.109+3512C=
ENST00000683328.1:c.109+3512C= ENSP00000508096.1:n.109+3512C=
ENST00000683380.1:n.390C=
ENST00000683398.1:c.70C=
ENST00000683551.1:c.109+1655C=
ENST00000683828.1:c.526-1619C=
ENST00000684259.1:n.577C=
ENST00000684549.1:n.368-1619C=
ENST00000684554.1:c.70C=
ENST00000261534.9:c.726C= MANE Select ENSP00000261534.4:p.Val242=
ENST00000261534.8:c.726C= ENSP00000261534.4:p.Val242=
ENST00000452340.7:n.749C=
ENST00000553863.5:n.390C=
ENST00000555675.5:n.442C=
ENST00000556326.5:c.*392C= ENSP00000450630.1:n.*392C=
ENST00000557289.1:c.56-1619C= ENSP00000451115.1:n.56-1619C=
NM_013382.5:c.726C= , LRG_844t1:c.726C= NP_037514.2:p.Val242=
XM_011536675.1:c.726C= XP_011534977.1:p.Val242=
XM_011536676.1:c.393C= XP_011534978.1:p.Val131=
XM_011536677.1:c.547+3512C= XP_011534979.1:n.547+3512C=
XM_011536678.1:c.726C= XP_011534980.1:p.Val242=
XM_011536679.1:c.-90-1619C= XP_011534981.1:n.-90-1619C=
XM_011536680.1:c.726C= XP_011534982.1:p.Val242=
XR_943416.1:n.929C=
XM_011536675.2:c.726C= XP_011534977.1:p.Val242=
XM_011536676.2:c.393C= XP_011534978.1:p.Val131=
XM_011536677.3:c.547+3512C= XP_011534979.1:n.547+3512C=
XR_001750279.1:n.926C=
XR_001750282.1:n.930C=
XR_943416.3:n.927C=
NM_013382.6:c.726C= NP_037514.2:p.Val242=
NM_013382.7:c.726C= MANE Select NP_037514.2:p.Val242=