Canonical Allele Identifier: CA2148327488
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278475G= , CM000676.2:g.77278475G= GRCh38
NC_000014.8:g.77744818G= , CM000676.1:g.77744818G= GRCh37
NC_000014.7:g.76814571G= NCBI36
NG_008897.1:g.47408C= , LRG_844:g.47408C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.991C=
ENST00000556394.2:c.1607C= ENSP00000451967.2:p.Ala536=
ENST00000682247.1:c.2055C= ENSP00000507213.1:p.Cys685=
ENST00000682395.1:n.2530C=
ENST00000682459.1:n.1769C=
ENST00000682467.1:c.1925C= ENSP00000508062.1:p.Ala642=
ENST00000682795.1:c.2213C= ENSP00000507574.1:p.Ala738=
ENST00000682895.1:n.1782C=
ENST00000682955.1:n.1640C=
ENST00000683188.1:c.2327C=
ENST00000683380.1:n.1730C=
ENST00000683907.1:c.331C= ENSP00000507754.1:n.331C=
ENST00000684259.1:n.3833C=
ENST00000684538.1:n.1445C=
ENST00000684549.1:n.1617C=
ENST00000261534.9:c.2066C= MANE Select ENSP00000261534.4:p.Ala689=
ENST00000261534.8:c.2066C= ENSP00000261534.4:p.Ala689=
ENST00000452340.7:n.3042C=
ENST00000554767.5:n.2852C=
ENST00000555710.1:c.427C= ENSP00000451730.1:n.427C=
ENST00000556394.1:c.121C=
ENST00000556446.1:n.367C=
ENST00000602717.5:c.281C= ENSP00000487704.1:p.Ala94=
NM_013382.5:c.2066C= , LRG_844t1:c.2066C= NP_037514.2:p.Ala689=
XM_011536675.1:c.2255C= XP_011534977.1:p.Ala752=
XM_011536676.1:c.1922C= XP_011534978.1:p.Ala641=
XM_011536677.1:c.1796C= XP_011534979.1:p.Ala599=
XM_011536679.1:c.1349C= XP_011534981.1:p.Ala450=
XR_943416.1:n.2319C=
XM_011536675.2:c.2255C= XP_011534977.1:p.Ala752=
XM_011536676.2:c.1922C= XP_011534978.1:p.Ala641=
XM_011536677.3:c.1796C= XP_011534979.1:p.Ala599=
XR_001750279.1:n.2352C=
XR_001750282.1:n.3005C=
XR_943416.3:n.2317C=
NM_013382.6:c.2066C= NP_037514.2:p.Ala689=
NM_013382.7:c.2066C= MANE Select NP_037514.2:p.Ala689=