Canonical Allele Identifier: CA2148327479
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278460G= , CM000676.2:g.77278460G= GRCh38
NC_000014.8:g.77744803G= , CM000676.1:g.77744803G= GRCh37
NC_000014.7:g.76814556G= NCBI36
NG_008897.1:g.47423C= , LRG_844:g.47423C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1006C=
ENST00000556394.2:c.1622C= ENSP00000451967.2:p.Ser541=
ENST00000682247.1:c.2070C= ENSP00000507213.1:p.Leu690=
ENST00000682395.1:n.2545C=
ENST00000682459.1:n.1784C=
ENST00000682467.1:c.1940C= ENSP00000508062.1:p.Ser647=
ENST00000682795.1:c.2228C= ENSP00000507574.1:p.Ser743=
ENST00000682895.1:n.1797C=
ENST00000682955.1:n.1655C=
ENST00000683188.1:c.2342C=
ENST00000683380.1:n.1745C=
ENST00000683907.1:c.346C= ENSP00000507754.1:n.346C=
ENST00000684259.1:n.3848C=
ENST00000684538.1:n.1460C=
ENST00000684549.1:n.1632C=
ENST00000261534.9:c.2081C= MANE Select ENSP00000261534.4:p.Ser694=
ENST00000261534.8:c.2081C= ENSP00000261534.4:p.Ser694=
ENST00000452340.7:n.3057C=
ENST00000554767.5:n.2867C=
ENST00000555710.1:c.442C= ENSP00000451730.1:n.442C=
ENST00000556394.1:c.136C=
ENST00000556446.1:n.382C=
ENST00000602717.5:c.296C= ENSP00000487704.1:p.Ser99=
NM_013382.5:c.2081C= , LRG_844t1:c.2081C= NP_037514.2:p.Ser694=
XM_011536675.1:c.2270C= XP_011534977.1:p.Ser757=
XM_011536676.1:c.1937C= XP_011534978.1:p.Ser646=
XM_011536677.1:c.1811C= XP_011534979.1:p.Ser604=
XM_011536679.1:c.1364C= XP_011534981.1:p.Ser455=
XR_943416.1:n.2334C=
XM_011536675.2:c.2270C= XP_011534977.1:p.Ser757=
XM_011536676.2:c.1937C= XP_011534978.1:p.Ser646=
XM_011536677.3:c.1811C= XP_011534979.1:p.Ser604=
XR_001750279.1:n.2367C=
XR_001750282.1:n.3020C=
XR_943416.3:n.2332C=
NM_013382.6:c.2081C= NP_037514.2:p.Ser694=
NM_013382.7:c.2081C= MANE Select NP_037514.2:p.Ser694=