Canonical Allele Identifier: CA2148327497
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278494T= , CM000676.2:g.77278494T= GRCh38
NC_000014.8:g.77744837T= , CM000676.1:g.77744837T= GRCh37
NC_000014.7:g.76814590T= NCBI36
NG_008897.1:g.47389A= , LRG_844:g.47389A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.972A=
ENST00000556394.2:c.1588A= ENSP00000451967.2:p.Thr530=
ENST00000682247.1:c.2036A= ENSP00000507213.1:p.His679=
ENST00000682395.1:n.2511A=
ENST00000682459.1:n.1750A=
ENST00000682467.1:c.1906A= ENSP00000508062.1:p.Thr636=
ENST00000682795.1:c.2194A= ENSP00000507574.1:p.Thr732=
ENST00000682895.1:n.1763A=
ENST00000682955.1:n.1621A=
ENST00000683188.1:c.2308A=
ENST00000683380.1:n.1711A=
ENST00000683907.1:c.312A= ENSP00000507754.1:n.312A=
ENST00000684259.1:n.3814A=
ENST00000684538.1:n.1426A=
ENST00000684549.1:n.1598A=
ENST00000261534.9:c.2047A= MANE Select ENSP00000261534.4:p.Thr683=
ENST00000261534.8:c.2047A= ENSP00000261534.4:p.Thr683=
ENST00000452340.7:n.3023A=
ENST00000554767.5:n.2833A=
ENST00000555710.1:c.408A= ENSP00000451730.1:n.408A=
ENST00000556394.1:c.102A=
ENST00000556446.1:n.348A=
ENST00000602717.5:c.262A= ENSP00000487704.1:p.Thr88=
NM_013382.5:c.2047A= , LRG_844t1:c.2047A= NP_037514.2:p.Thr683=
XM_011536675.1:c.2236A= XP_011534977.1:p.Thr746=
XM_011536676.1:c.1903A= XP_011534978.1:p.Thr635=
XM_011536677.1:c.1777A= XP_011534979.1:p.Thr593=
XM_011536679.1:c.1330A= XP_011534981.1:p.Thr444=
XR_943416.1:n.2300A=
XM_011536675.2:c.2236A= XP_011534977.1:p.Thr746=
XM_011536676.2:c.1903A= XP_011534978.1:p.Thr635=
XM_011536677.3:c.1777A= XP_011534979.1:p.Thr593=
XR_001750279.1:n.2333A=
XR_001750282.1:n.2986A=
XR_943416.3:n.2298A=
NM_013382.6:c.2047A= NP_037514.2:p.Thr683=
NM_013382.7:c.2047A= MANE Select NP_037514.2:p.Thr683=