Canonical Allele Identifier: CA2148327502
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278506T= , CM000676.2:g.77278506T= GRCh38
NC_000014.8:g.77744849T= , CM000676.1:g.77744849T= GRCh37
NC_000014.7:g.76814602T= NCBI36
NG_008897.1:g.47377A= , LRG_844:g.47377A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.960A=
ENST00000556394.2:c.1576A= ENSP00000451967.2:p.Ile526=
ENST00000682247.1:c.2024A= ENSP00000507213.1:p.His675=
ENST00000682395.1:n.2499A=
ENST00000682459.1:n.1738A=
ENST00000682467.1:c.1894A= ENSP00000508062.1:p.Ile632=
ENST00000682795.1:c.2182A= ENSP00000507574.1:p.Ile728=
ENST00000682895.1:n.1751A=
ENST00000682955.1:n.1609A=
ENST00000683188.1:c.2296A=
ENST00000683380.1:n.1699A=
ENST00000683907.1:c.300A= ENSP00000507754.1:n.300A=
ENST00000684259.1:n.3802A=
ENST00000684538.1:n.1414A=
ENST00000684549.1:n.1586A=
ENST00000261534.9:c.2035A= MANE Select ENSP00000261534.4:p.Ile679=
ENST00000261534.8:c.2035A= ENSP00000261534.4:p.Ile679=
ENST00000452340.7:n.3011A=
ENST00000554767.5:n.2821A=
ENST00000555710.1:c.396A= ENSP00000451730.1:n.396A=
ENST00000556394.1:c.90A=
ENST00000556446.1:n.336A=
ENST00000602717.5:c.250A= ENSP00000487704.1:p.Ile84=
NM_013382.5:c.2035A= , LRG_844t1:c.2035A= NP_037514.2:p.Ile679=
XM_011536675.1:c.2224A= XP_011534977.1:p.Ile742=
XM_011536676.1:c.1891A= XP_011534978.1:p.Ile631=
XM_011536677.1:c.1765A= XP_011534979.1:p.Ile589=
XM_011536679.1:c.1318A= XP_011534981.1:p.Ile440=
XR_943416.1:n.2288A=
XM_011536675.2:c.2224A= XP_011534977.1:p.Ile742=
XM_011536676.2:c.1891A= XP_011534978.1:p.Ile631=
XM_011536677.3:c.1765A= XP_011534979.1:p.Ile589=
XR_001750279.1:n.2321A=
XR_001750282.1:n.2974A=
XR_943416.3:n.2286A=
NM_013382.6:c.2035A= NP_037514.2:p.Ile679=
NM_013382.7:c.2035A= MANE Select NP_037514.2:p.Ile679=