Canonical Allele Identifier: CA2148327477
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278458A= , CM000676.2:g.77278458A= GRCh38
NC_000014.8:g.77744801A= , CM000676.1:g.77744801A= GRCh37
NC_000014.7:g.76814554A= NCBI36
NG_008897.1:g.47425T= , LRG_844:g.47425T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1008T=
ENST00000556394.2:c.1624T= ENSP00000451967.2:p.Trp542=
ENST00000682247.1:c.2072T= ENSP00000507213.1:p.Met691=
ENST00000682395.1:n.2547T=
ENST00000682459.1:n.1786T=
ENST00000682467.1:c.1942T= ENSP00000508062.1:p.Trp648=
ENST00000682795.1:c.2230T= ENSP00000507574.1:p.Trp744=
ENST00000682895.1:n.1799T=
ENST00000682955.1:n.1657T=
ENST00000683188.1:c.2344T=
ENST00000683380.1:n.1747T=
ENST00000683907.1:c.348T= ENSP00000507754.1:n.348T=
ENST00000684259.1:n.3850T=
ENST00000684538.1:n.1462T=
ENST00000684549.1:n.1634T=
ENST00000261534.9:c.2083T= MANE Select ENSP00000261534.4:p.Trp695=
ENST00000261534.8:c.2083T= ENSP00000261534.4:p.Trp695=
ENST00000452340.7:n.3059T=
ENST00000554767.5:n.2869T=
ENST00000555710.1:c.444T= ENSP00000451730.1:n.444T=
ENST00000556394.1:c.138T=
ENST00000556446.1:n.384T=
ENST00000602717.5:c.298T= ENSP00000487704.1:p.Trp100=
NM_013382.5:c.2083T= , LRG_844t1:c.2083T= NP_037514.2:p.Trp695=
XM_011536675.1:c.2272T= XP_011534977.1:p.Trp758=
XM_011536676.1:c.1939T= XP_011534978.1:p.Trp647=
XM_011536677.1:c.1813T= XP_011534979.1:p.Trp605=
XM_011536679.1:c.1366T= XP_011534981.1:p.Trp456=
XR_943416.1:n.2336T=
XM_011536675.2:c.2272T= XP_011534977.1:p.Trp758=
XM_011536676.2:c.1939T= XP_011534978.1:p.Trp647=
XM_011536677.3:c.1813T= XP_011534979.1:p.Trp605=
XR_001750279.1:n.2369T=
XR_001750282.1:n.3022T=
XR_943416.3:n.2334T=
NM_013382.6:c.2083T= NP_037514.2:p.Trp695=
NM_013382.7:c.2083T= MANE Select NP_037514.2:p.Trp695=