Canonical Allele Identifier: CA390513507
Gene: POMT2 HGNC NCBI

Linked Data

dbSNP Id: rs398124263

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278456C>T , CM000676.2:g.77278456C>T GRCh38
NC_000014.8:g.77744799C>T , CM000676.1:g.77744799C>T GRCh37
NC_000014.7:g.76814552C>T NCBI36
NG_008897.1:g.47427G>A , LRG_844:g.47427G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1010G>A
ENST00000556394.2:c.1626G>A ENSP00000451967.2:p.Trp542Ter
ENST00000682247.1:c.2074G>A ENSP00000507213.1:p.Ala692Thr
ENST00000682395.1:n.2549G>A
ENST00000682459.1:n.1788G>A
ENST00000682467.1:c.1944G>A ENSP00000508062.1:p.Trp648Ter
ENST00000682795.1:c.2232G>A ENSP00000507574.1:p.Trp744Ter
ENST00000682895.1:n.1801G>A
ENST00000682955.1:n.1659G>A
ENST00000683188.1:c.2346G>A
ENST00000683380.1:n.1749G>A
ENST00000683907.1:c.350G>A ENSP00000507754.1:n.350G>A
ENST00000684259.1:n.3852G>A
ENST00000684538.1:n.1464G>A
ENST00000684549.1:n.1636G>A
ENST00000261534.9:c.2085G>A MANE Select ENSP00000261534.4:p.Trp695Ter
ENST00000261534.8:c.2085G>A ENSP00000261534.4:p.Trp695Ter
ENST00000452340.7:n.3061G>A
ENST00000554767.5:n.2871G>A
ENST00000555710.1:c.446G>A ENSP00000451730.1:n.446G>A
ENST00000556394.1:c.140G>A
ENST00000556446.1:n.386G>A
ENST00000602717.5:c.300G>A ENSP00000487704.1:p.Trp100Ter
NM_013382.5:c.2085G>A , LRG_844t1:c.2085G>A NP_037514.2:p.Trp695Ter
XM_011536675.1:c.2274G>A XP_011534977.1:p.Trp758Ter
XM_011536676.1:c.1941G>A XP_011534978.1:p.Trp647Ter
XM_011536677.1:c.1815G>A XP_011534979.1:p.Trp605Ter
XM_011536679.1:c.1368G>A XP_011534981.1:p.Trp456Ter
XR_943416.1:n.2338G>A
XM_011536675.2:c.2274G>A XP_011534977.1:p.Trp758Ter
XM_011536676.2:c.1941G>A XP_011534978.1:p.Trp647Ter
XM_011536677.3:c.1815G>A XP_011534979.1:p.Trp605Ter
XR_001750279.1:n.2371G>A
XR_001750282.1:n.3024G>A
XR_943416.3:n.2336G>A
NM_013382.6:c.2085G>A NP_037514.2:p.Trp695Ter
NM_013382.7:c.2085G>A MANE Select NP_037514.2:p.Trp695Ter