Canonical Allele Identifier: CA2148327472
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278453G= , CM000676.2:g.77278453G= GRCh38
NC_000014.8:g.77744796G= , CM000676.1:g.77744796G= GRCh37
NC_000014.7:g.76814549G= NCBI36
NG_008897.1:g.47430C= , LRG_844:g.47430C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1013C=
ENST00000556394.2:c.1629C= ENSP00000451967.2:p.Pro543=
ENST00000682247.1:c.2077C= ENSP00000507213.1:p.Pro693=
ENST00000682395.1:n.2552C=
ENST00000682459.1:n.1791C=
ENST00000682467.1:c.1947C= ENSP00000508062.1:p.Pro649=
ENST00000682795.1:c.2235C= ENSP00000507574.1:p.Pro745=
ENST00000682895.1:n.1804C=
ENST00000682955.1:n.1662C=
ENST00000683188.1:c.2349C=
ENST00000683380.1:n.1752C=
ENST00000683907.1:c.353C= ENSP00000507754.1:n.353C=
ENST00000684259.1:n.3855C=
ENST00000684538.1:n.1467C=
ENST00000684549.1:n.1639C=
ENST00000261534.9:c.2088C= MANE Select ENSP00000261534.4:p.Pro696=
ENST00000261534.8:c.2088C= ENSP00000261534.4:p.Pro696=
ENST00000452340.7:n.3064C=
ENST00000554767.5:n.2874C=
ENST00000555710.1:c.449C= ENSP00000451730.1:n.449C=
ENST00000556394.1:c.143C=
ENST00000556446.1:n.389C=
ENST00000602717.5:c.303C= ENSP00000487704.1:p.Pro101=
NM_013382.5:c.2088C= , LRG_844t1:c.2088C= NP_037514.2:p.Pro696=
XM_011536675.1:c.2277C= XP_011534977.1:p.Pro759=
XM_011536676.1:c.1944C= XP_011534978.1:p.Pro648=
XM_011536677.1:c.1818C= XP_011534979.1:p.Pro606=
XM_011536679.1:c.1371C= XP_011534981.1:p.Pro457=
XR_943416.1:n.2341C=
XM_011536675.2:c.2277C= XP_011534977.1:p.Pro759=
XM_011536676.2:c.1944C= XP_011534978.1:p.Pro648=
XM_011536677.3:c.1818C= XP_011534979.1:p.Pro606=
XR_001750279.1:n.2374C=
XR_001750282.1:n.3027C=
XR_943416.3:n.2339C=
NM_013382.6:c.2088C= NP_037514.2:p.Pro696=
NM_013382.7:c.2088C= MANE Select NP_037514.2:p.Pro696=