Canonical Allele Identifier: CA2148327493
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278487A= , CM000676.2:g.77278487A= GRCh38
NC_000014.8:g.77744830A= , CM000676.1:g.77744830A= GRCh37
NC_000014.7:g.76814583A= NCBI36
NG_008897.1:g.47396T= , LRG_844:g.47396T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.979T=
ENST00000556394.2:c.1595T= ENSP00000451967.2:p.Leu532=
ENST00000682247.1:c.2043T= ENSP00000507213.1:p.Pro681=
ENST00000682395.1:n.2518T=
ENST00000682459.1:n.1757T=
ENST00000682467.1:c.1913T= ENSP00000508062.1:p.Leu638=
ENST00000682795.1:c.2201T= ENSP00000507574.1:p.Leu734=
ENST00000682895.1:n.1770T=
ENST00000682955.1:n.1628T=
ENST00000683188.1:c.2315T=
ENST00000683380.1:n.1718T=
ENST00000683907.1:c.319T= ENSP00000507754.1:n.319T=
ENST00000684259.1:n.3821T=
ENST00000684538.1:n.1433T=
ENST00000684549.1:n.1605T=
ENST00000261534.9:c.2054T= MANE Select ENSP00000261534.4:p.Leu685=
ENST00000261534.8:c.2054T= ENSP00000261534.4:p.Leu685=
ENST00000452340.7:n.3030T=
ENST00000554767.5:n.2840T=
ENST00000555710.1:c.415T= ENSP00000451730.1:n.415T=
ENST00000556394.1:c.109T=
ENST00000556446.1:n.355T=
ENST00000602717.5:c.269T= ENSP00000487704.1:p.Leu90=
NM_013382.5:c.2054T= , LRG_844t1:c.2054T= NP_037514.2:p.Leu685=
XM_011536675.1:c.2243T= XP_011534977.1:p.Leu748=
XM_011536676.1:c.1910T= XP_011534978.1:p.Leu637=
XM_011536677.1:c.1784T= XP_011534979.1:p.Leu595=
XM_011536679.1:c.1337T= XP_011534981.1:p.Leu446=
XR_943416.1:n.2307T=
XM_011536675.2:c.2243T= XP_011534977.1:p.Leu748=
XM_011536676.2:c.1910T= XP_011534978.1:p.Leu637=
XM_011536677.3:c.1784T= XP_011534979.1:p.Leu595=
XR_001750279.1:n.2340T=
XR_001750282.1:n.2993T=
XR_943416.3:n.2305T=
NM_013382.6:c.2054T= NP_037514.2:p.Leu685=
NM_013382.7:c.2054T= MANE Select NP_037514.2:p.Leu685=