Canonical Allele Identifier: CA7285581
Community Standard Title: NM_013382.7(POMT2):c.1976G>A (p.Arg659Gln)
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278785C>T , CM000676.2:g.77278785C>T GRCh38
NC_000014.8:g.77745128C>T , CM000676.1:g.77745128C>T GRCh37
NC_000014.7:g.76814881C>T NCBI36
NG_008897.1:g.47098G>A , LRG_844:g.47098G>A

Transcript Alleles

HGVS Amino-acid Change
NM_013382.7:c.1976G>A MANE Select NP_037514.2:p.Arg659Gln
ENST00000261534.9:c.1976G>A MANE Select ENSP00000261534.4:p.Arg659Gln
NM_013382.5:c.1976G>A , LRG_844t1:c.1976G>A NP_037514.2:p.Arg659Gln
NM_013382.6:c.1976G>A NP_037514.2:p.Arg659Gln
ENST00000261534.8:c.1976G>A ENSP00000261534.4:p.Arg659Gln
ENST00000452340.7:n.2952G>A
ENST00000554767.5:n.2762G>A
ENST00000555134.2:n.901G>A
ENST00000555710.1:c.337G>A ENSP00000451730.1:n.337G>A
ENST00000556171.1:c.568G>A
ENST00000556394.1:c.88-277G>A
ENST00000556394.2:c.1517G>A ENSP00000451967.2:p.Arg506Gln
ENST00000556446.1:n.277G>A
ENST00000602717.5:c.191G>A ENSP00000487704.1:p.Arg64Gln
ENST00000682128.1:c.277G>A ENSP00000506976.1:n.277G>A
ENST00000682247.1:c.1965G>A ENSP00000507213.1:p.Pro655=
ENST00000682395.1:n.2440G>A
ENST00000682459.1:n.1679G>A
ENST00000682467.1:c.1892-277G>A ENSP00000508062.1:n.1892-277G>A
ENST00000682615.1:n.330G>A
ENST00000682795.1:c.2123G>A ENSP00000507574.1:p.Arg708Gln
ENST00000682895.1:n.1692G>A
ENST00000682955.1:n.1550G>A
ENST00000683095.1:c.382G>A ENSP00000508040.1:n.382G>A
ENST00000683188.1:c.2237G>A
ENST00000683380.1:n.1640G>A
ENST00000683828.1:c.1685G>A
ENST00000683907.1:c.241G>A ENSP00000507754.1:n.241G>A
ENST00000684172.1:c.352G>A ENSP00000508391.1:n.352G>A
ENST00000684259.1:n.3743G>A
ENST00000684538.1:n.1355G>A
ENST00000684549.1:n.1527G>A
XM_011536675.1:c.2165G>A XP_011534977.1:p.Arg722Gln
XM_011536675.2:c.2165G>A XP_011534977.1:p.Arg722Gln
XM_011536676.1:c.1832G>A XP_011534978.1:p.Arg611Gln
XM_011536676.2:c.1832G>A XP_011534978.1:p.Arg611Gln
XM_011536677.1:c.1706G>A XP_011534979.1:p.Arg569Gln
XM_011536677.3:c.1706G>A XP_011534979.1:p.Arg569Gln
XM_011536679.1:c.1259G>A XP_011534981.1:p.Arg420Gln
XR_001750279.1:n.2262G>A
XR_001750282.1:n.2915G>A
XR_943416.1:n.2229G>A
XR_943416.3:n.2227G>A