Canonical Allele Identifier: CA2148327491
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278485G= , CM000676.2:g.77278485G= GRCh38
NC_000014.8:g.77744828G= , CM000676.1:g.77744828G= GRCh37
NC_000014.7:g.76814581G= NCBI36
NG_008897.1:g.47398C= , LRG_844:g.47398C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.981C=
ENST00000556394.2:c.1597C= ENSP00000451967.2:p.Arg533=
ENST00000682247.1:c.2045C= ENSP00000507213.1:p.Ala682=
ENST00000682395.1:n.2520C=
ENST00000682459.1:n.1759C=
ENST00000682467.1:c.1915C= ENSP00000508062.1:p.Arg639=
ENST00000682795.1:c.2203C= ENSP00000507574.1:p.Arg735=
ENST00000682895.1:n.1772C=
ENST00000682955.1:n.1630C=
ENST00000683188.1:c.2317C=
ENST00000683380.1:n.1720C=
ENST00000683907.1:c.321C= ENSP00000507754.1:n.321C=
ENST00000684259.1:n.3823C=
ENST00000684538.1:n.1435C=
ENST00000684549.1:n.1607C=
ENST00000261534.9:c.2056C= MANE Select ENSP00000261534.4:p.Arg686=
ENST00000261534.8:c.2056C= ENSP00000261534.4:p.Arg686=
ENST00000452340.7:n.3032C=
ENST00000554767.5:n.2842C=
ENST00000555710.1:c.417C= ENSP00000451730.1:n.417C=
ENST00000556394.1:c.111C=
ENST00000556446.1:n.357C=
ENST00000602717.5:c.271C= ENSP00000487704.1:p.Arg91=
NM_013382.5:c.2056C= , LRG_844t1:c.2056C= NP_037514.2:p.Arg686=
XM_011536675.1:c.2245C= XP_011534977.1:p.Arg749=
XM_011536676.1:c.1912C= XP_011534978.1:p.Arg638=
XM_011536677.1:c.1786C= XP_011534979.1:p.Arg596=
XM_011536679.1:c.1339C= XP_011534981.1:p.Arg447=
XR_943416.1:n.2309C=
XM_011536675.2:c.2245C= XP_011534977.1:p.Arg749=
XM_011536676.2:c.1912C= XP_011534978.1:p.Arg638=
XM_011536677.3:c.1786C= XP_011534979.1:p.Arg596=
XR_001750279.1:n.2342C=
XR_001750282.1:n.2995C=
XR_943416.3:n.2307C=
NM_013382.6:c.2056C= NP_037514.2:p.Arg686=
NM_013382.7:c.2056C= MANE Select NP_037514.2:p.Arg686=