Canonical Allele Identifier: CA2148327486
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278470C= , CM000676.2:g.77278470C= GRCh38
NC_000014.8:g.77744813C= , CM000676.1:g.77744813C= GRCh37
NC_000014.7:g.76814566C= NCBI36
NG_008897.1:g.47413G= , LRG_844:g.47413G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.996G=
ENST00000556394.2:c.1612G= ENSP00000451967.2:p.Gly538=
ENST00000682247.1:c.2060G= ENSP00000507213.1:p.Gly687=
ENST00000682395.1:n.2535G=
ENST00000682459.1:n.1774G=
ENST00000682467.1:c.1930G= ENSP00000508062.1:p.Gly644=
ENST00000682795.1:c.2218G= ENSP00000507574.1:p.Gly740=
ENST00000682895.1:n.1787G=
ENST00000682955.1:n.1645G=
ENST00000683188.1:c.2332G=
ENST00000683380.1:n.1735G=
ENST00000683907.1:c.336G= ENSP00000507754.1:n.336G=
ENST00000684259.1:n.3838G=
ENST00000684538.1:n.1450G=
ENST00000684549.1:n.1622G=
ENST00000261534.9:c.2071G= MANE Select ENSP00000261534.4:p.Gly691=
ENST00000261534.8:c.2071G= ENSP00000261534.4:p.Gly691=
ENST00000452340.7:n.3047G=
ENST00000554767.5:n.2857G=
ENST00000555710.1:c.432G= ENSP00000451730.1:n.432G=
ENST00000556394.1:c.126G=
ENST00000556446.1:n.372G=
ENST00000602717.5:c.286G= ENSP00000487704.1:p.Gly96=
NM_013382.5:c.2071G= , LRG_844t1:c.2071G= NP_037514.2:p.Gly691=
XM_011536675.1:c.2260G= XP_011534977.1:p.Gly754=
XM_011536676.1:c.1927G= XP_011534978.1:p.Gly643=
XM_011536677.1:c.1801G= XP_011534979.1:p.Gly601=
XM_011536679.1:c.1354G= XP_011534981.1:p.Gly452=
XR_943416.1:n.2324G=
XM_011536675.2:c.2260G= XP_011534977.1:p.Gly754=
XM_011536676.2:c.1927G= XP_011534978.1:p.Gly643=
XM_011536677.3:c.1801G= XP_011534979.1:p.Gly601=
XR_001750279.1:n.2357G=
XR_001750282.1:n.3010G=
XR_943416.3:n.2322G=
NM_013382.6:c.2071G= NP_037514.2:p.Gly691=
NM_013382.7:c.2071G= MANE Select NP_037514.2:p.Gly691=