Canonical Allele Identifier: CA2148327476
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278456C= , CM000676.2:g.77278456C= GRCh38
NC_000014.8:g.77744799C= , CM000676.1:g.77744799C= GRCh37
NC_000014.7:g.76814552C= NCBI36
NG_008897.1:g.47427G= , LRG_844:g.47427G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1010G=
ENST00000556394.2:c.1626G= ENSP00000451967.2:p.Trp542=
ENST00000682247.1:c.2074G= ENSP00000507213.1:p.Ala692=
ENST00000682395.1:n.2549G=
ENST00000682459.1:n.1788G=
ENST00000682467.1:c.1944G= ENSP00000508062.1:p.Trp648=
ENST00000682795.1:c.2232G= ENSP00000507574.1:p.Trp744=
ENST00000682895.1:n.1801G=
ENST00000682955.1:n.1659G=
ENST00000683188.1:c.2346G=
ENST00000683380.1:n.1749G=
ENST00000683907.1:c.350G= ENSP00000507754.1:n.350G=
ENST00000684259.1:n.3852G=
ENST00000684538.1:n.1464G=
ENST00000684549.1:n.1636G=
ENST00000261534.9:c.2085G= MANE Select ENSP00000261534.4:p.Trp695=
ENST00000261534.8:c.2085G= ENSP00000261534.4:p.Trp695=
ENST00000452340.7:n.3061G=
ENST00000554767.5:n.2871G=
ENST00000555710.1:c.446G= ENSP00000451730.1:n.446G=
ENST00000556394.1:c.140G=
ENST00000556446.1:n.386G=
ENST00000602717.5:c.300G= ENSP00000487704.1:p.Trp100=
NM_013382.5:c.2085G= , LRG_844t1:c.2085G= NP_037514.2:p.Trp695=
XM_011536675.1:c.2274G= XP_011534977.1:p.Trp758=
XM_011536676.1:c.1941G= XP_011534978.1:p.Trp647=
XM_011536677.1:c.1815G= XP_011534979.1:p.Trp605=
XM_011536679.1:c.1368G= XP_011534981.1:p.Trp456=
XR_943416.1:n.2338G=
XM_011536675.2:c.2274G= XP_011534977.1:p.Trp758=
XM_011536676.2:c.1941G= XP_011534978.1:p.Trp647=
XM_011536677.3:c.1815G= XP_011534979.1:p.Trp605=
XR_001750279.1:n.2371G=
XR_001750282.1:n.3024G=
XR_943416.3:n.2336G=
NM_013382.6:c.2085G= NP_037514.2:p.Trp695=
NM_013382.7:c.2085G= MANE Select NP_037514.2:p.Trp695=