Canonical Allele Identifier: CA2148327471
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278451A= , CM000676.2:g.77278451A= GRCh38
NC_000014.8:g.77744794A= , CM000676.1:g.77744794A= GRCh37
NC_000014.7:g.76814547A= NCBI36
NG_008897.1:g.47432T= , LRG_844:g.47432T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1015T=
ENST00000556394.2:c.1631T= ENSP00000451967.2:p.Leu544=
ENST00000682247.1:c.2079T= ENSP00000507213.1:p.Pro693=
ENST00000682395.1:n.2554T=
ENST00000682459.1:n.1793T=
ENST00000682467.1:c.1949T= ENSP00000508062.1:p.Leu650=
ENST00000682795.1:c.2237T= ENSP00000507574.1:p.Leu746=
ENST00000682895.1:n.1806T=
ENST00000682955.1:n.1664T=
ENST00000683188.1:c.2351T=
ENST00000683380.1:n.1754T=
ENST00000683907.1:c.355T= ENSP00000507754.1:n.355T=
ENST00000684259.1:n.3857T=
ENST00000684538.1:n.1469T=
ENST00000684549.1:n.1641T=
ENST00000261534.9:c.2090T= MANE Select ENSP00000261534.4:p.Leu697=
ENST00000261534.8:c.2090T= ENSP00000261534.4:p.Leu697=
ENST00000452340.7:n.3066T=
ENST00000554767.5:n.2876T=
ENST00000555710.1:c.451T= ENSP00000451730.1:n.451T=
ENST00000556394.1:c.145T=
ENST00000556446.1:n.391T=
ENST00000602717.5:c.305T= ENSP00000487704.1:p.Leu102=
NM_013382.5:c.2090T= , LRG_844t1:c.2090T= NP_037514.2:p.Leu697=
XM_011536675.1:c.2279T= XP_011534977.1:p.Leu760=
XM_011536676.1:c.1946T= XP_011534978.1:p.Leu649=
XM_011536677.1:c.1820T= XP_011534979.1:p.Leu607=
XM_011536679.1:c.1373T= XP_011534981.1:p.Leu458=
XR_943416.1:n.2343T=
XM_011536675.2:c.2279T= XP_011534977.1:p.Leu760=
XM_011536676.2:c.1946T= XP_011534978.1:p.Leu649=
XM_011536677.3:c.1820T= XP_011534979.1:p.Leu607=
XR_001750279.1:n.2376T=
XR_001750282.1:n.3029T=
XR_943416.3:n.2341T=
NM_013382.6:c.2090T= NP_037514.2:p.Leu697=
NM_013382.7:c.2090T= MANE Select NP_037514.2:p.Leu697=