Canonical Allele Identifier: CA2148327478
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278459T= , CM000676.2:g.77278459T= GRCh38
NC_000014.8:g.77744802T= , CM000676.1:g.77744802T= GRCh37
NC_000014.7:g.76814555T= NCBI36
NG_008897.1:g.47424A= , LRG_844:g.47424A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1007A=
ENST00000556394.2:c.1623A= ENSP00000451967.2:p.Ser541=
ENST00000682247.1:c.2071A= ENSP00000507213.1:p.Met691=
ENST00000682395.1:n.2546A=
ENST00000682459.1:n.1785A=
ENST00000682467.1:c.1941A= ENSP00000508062.1:p.Ser647=
ENST00000682795.1:c.2229A= ENSP00000507574.1:p.Ser743=
ENST00000682895.1:n.1798A=
ENST00000682955.1:n.1656A=
ENST00000683188.1:c.2343A=
ENST00000683380.1:n.1746A=
ENST00000683907.1:c.347A= ENSP00000507754.1:n.347A=
ENST00000684259.1:n.3849A=
ENST00000684538.1:n.1461A=
ENST00000684549.1:n.1633A=
ENST00000261534.9:c.2082A= MANE Select ENSP00000261534.4:p.Ser694=
ENST00000261534.8:c.2082A= ENSP00000261534.4:p.Ser694=
ENST00000452340.7:n.3058A=
ENST00000554767.5:n.2868A=
ENST00000555710.1:c.443A= ENSP00000451730.1:n.443A=
ENST00000556394.1:c.137A=
ENST00000556446.1:n.383A=
ENST00000602717.5:c.297A= ENSP00000487704.1:p.Ser99=
NM_013382.5:c.2082A= , LRG_844t1:c.2082A= NP_037514.2:p.Ser694=
XM_011536675.1:c.2271A= XP_011534977.1:p.Ser757=
XM_011536676.1:c.1938A= XP_011534978.1:p.Ser646=
XM_011536677.1:c.1812A= XP_011534979.1:p.Ser604=
XM_011536679.1:c.1365A= XP_011534981.1:p.Ser455=
XR_943416.1:n.2335A=
XM_011536675.2:c.2271A= XP_011534977.1:p.Ser757=
XM_011536676.2:c.1938A= XP_011534978.1:p.Ser646=
XM_011536677.3:c.1812A= XP_011534979.1:p.Ser604=
XR_001750279.1:n.2368A=
XR_001750282.1:n.3021A=
XR_943416.3:n.2333A=
NM_013382.6:c.2082A= NP_037514.2:p.Ser694=
NM_013382.7:c.2082A= MANE Select NP_037514.2:p.Ser694=