Canonical Allele Identifier: CA2148342214
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77300986A= , CM000676.2:g.77300986A= GRCh38
NC_000014.8:g.77767329A= , CM000676.1:g.77767329A= GRCh37
NC_000014.7:g.76837082A= NCBI36
NG_008897.1:g.24897T= , LRG_844:g.24897T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553863.6:c.269+104T= ENSP00000508202.1:n.269+104T=
ENST00000556394.2:c.358-1425T= ENSP00000451967.2:n.358-1425T=
ENST00000557289.2:c.160+104T=
ENST00000682247.1:c.816+104T= ENSP00000507213.1:n.816+104T=
ENST00000682382.1:c.496-2215T=
ENST00000682395.1:n.545+104T=
ENST00000682459.1:n.480+104T=
ENST00000682467.1:c.816+104T= ENSP00000508062.1:n.816+104T=
ENST00000682795.1:c.816+104T= ENSP00000507574.1:n.816+104T=
ENST00000682895.1:n.532+104T=
ENST00000682955.1:n.212-2215T=
ENST00000683167.1:c.160+104T=
ENST00000683188.1:c.343-1425T=
ENST00000683300.1:c.109+3706T= ENSP00000507630.1:n.109+3706T=
ENST00000683328.1:c.109+3706T= ENSP00000508096.1:n.109+3706T=
ENST00000683380.1:n.480+104T=
ENST00000683398.1:c.176T=
ENST00000683551.1:c.109+1849T=
ENST00000683828.1:c.526-1425T=
ENST00000684259.1:n.667+104T=
ENST00000684549.1:n.368-1425T=
ENST00000684554.1:c.160+104T=
ENST00000261534.9:c.816+104T= MANE Select ENSP00000261534.4:n.816+104T=
ENST00000261534.8:c.816+104T= ENSP00000261534.4:n.816+104T=
ENST00000452340.7:n.839+104T=
ENST00000553863.5:n.480+104T=
ENST00000554767.5:n.178T=
ENST00000556326.5:c.*482+104T= ENSP00000450630.1:n.*482+104T=
ENST00000557289.1:c.56-1425T= ENSP00000451115.1:n.56-1425T=
NM_013382.5:c.816+104T= , LRG_844t1:c.816+104T= NP_037514.2:n.816+104T=
XM_011536675.1:c.816+104T= XP_011534977.1:n.816+104T=
XM_011536676.1:c.483+104T= XP_011534978.1:n.483+104T=
XM_011536677.1:c.547+3706T= XP_011534979.1:n.547+3706T=
XM_011536678.1:c.816+104T= XP_011534980.1:n.816+104T=
XM_011536679.1:c.-90-1425T= XP_011534981.1:n.-90-1425T=
XM_011536680.1:c.816+104T= XP_011534982.1:n.816+104T=
XR_943416.1:n.1019+104T=
XM_011536675.2:c.816+104T= XP_011534977.1:n.816+104T=
XM_011536676.2:c.483+104T= XP_011534978.1:n.483+104T=
XM_011536677.3:c.547+3706T= XP_011534979.1:n.547+3706T=
XR_001750279.1:n.1016+104T=
XR_001750282.1:n.1020+104T=
XR_943416.3:n.1017+104T=
NM_013382.6:c.816+104T= NP_037514.2:n.816+104T=
NM_013382.7:c.816+104T= MANE Select NP_037514.2:n.816+104T=