Canonical Allele Identifier: CA2148327492
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278486C= , CM000676.2:g.77278486C= GRCh38
NC_000014.8:g.77744829C= , CM000676.1:g.77744829C= GRCh37
NC_000014.7:g.76814582C= NCBI36
NG_008897.1:g.47397G= , LRG_844:g.47397G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.980G=
ENST00000556394.2:c.1596G= ENSP00000451967.2:p.Leu532=
ENST00000682247.1:c.2044G= ENSP00000507213.1:p.Ala682=
ENST00000682395.1:n.2519G=
ENST00000682459.1:n.1758G=
ENST00000682467.1:c.1914G= ENSP00000508062.1:p.Leu638=
ENST00000682795.1:c.2202G= ENSP00000507574.1:p.Leu734=
ENST00000682895.1:n.1771G=
ENST00000682955.1:n.1629G=
ENST00000683188.1:c.2316G=
ENST00000683380.1:n.1719G=
ENST00000683907.1:c.320G= ENSP00000507754.1:n.320G=
ENST00000684259.1:n.3822G=
ENST00000684538.1:n.1434G=
ENST00000684549.1:n.1606G=
ENST00000261534.9:c.2055G= MANE Select ENSP00000261534.4:p.Leu685=
ENST00000261534.8:c.2055G= ENSP00000261534.4:p.Leu685=
ENST00000452340.7:n.3031G=
ENST00000554767.5:n.2841G=
ENST00000555710.1:c.416G= ENSP00000451730.1:n.416G=
ENST00000556394.1:c.110G=
ENST00000556446.1:n.356G=
ENST00000602717.5:c.270G= ENSP00000487704.1:p.Leu90=
NM_013382.5:c.2055G= , LRG_844t1:c.2055G= NP_037514.2:p.Leu685=
XM_011536675.1:c.2244G= XP_011534977.1:p.Leu748=
XM_011536676.1:c.1911G= XP_011534978.1:p.Leu637=
XM_011536677.1:c.1785G= XP_011534979.1:p.Leu595=
XM_011536679.1:c.1338G= XP_011534981.1:p.Leu446=
XR_943416.1:n.2308G=
XM_011536675.2:c.2244G= XP_011534977.1:p.Leu748=
XM_011536676.2:c.1911G= XP_011534978.1:p.Leu637=
XM_011536677.3:c.1785G= XP_011534979.1:p.Leu595=
XR_001750279.1:n.2341G=
XR_001750282.1:n.2994G=
XR_943416.3:n.2306G=
NM_013382.6:c.2055G= NP_037514.2:p.Leu685=
NM_013382.7:c.2055G= MANE Select NP_037514.2:p.Leu685=