Canonical Allele Identifier: CA2148327482
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278465C= , CM000676.2:g.77278465C= GRCh38
NC_000014.8:g.77744808C= , CM000676.1:g.77744808C= GRCh37
NC_000014.7:g.76814561C= NCBI36
NG_008897.1:g.47418G= , LRG_844:g.47418G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1001G=
ENST00000556394.2:c.1617G= ENSP00000451967.2:p.Leu539=
ENST00000682247.1:c.2065G= ENSP00000507213.1:p.Gly689=
ENST00000682395.1:n.2540G=
ENST00000682459.1:n.1779G=
ENST00000682467.1:c.1935G= ENSP00000508062.1:p.Leu645=
ENST00000682795.1:c.2223G= ENSP00000507574.1:p.Leu741=
ENST00000682895.1:n.1792G=
ENST00000682955.1:n.1650G=
ENST00000683188.1:c.2337G=
ENST00000683380.1:n.1740G=
ENST00000683907.1:c.341G= ENSP00000507754.1:n.341G=
ENST00000684259.1:n.3843G=
ENST00000684538.1:n.1455G=
ENST00000684549.1:n.1627G=
ENST00000261534.9:c.2076G= MANE Select ENSP00000261534.4:p.Leu692=
ENST00000261534.8:c.2076G= ENSP00000261534.4:p.Leu692=
ENST00000452340.7:n.3052G=
ENST00000554767.5:n.2862G=
ENST00000555710.1:c.437G= ENSP00000451730.1:n.437G=
ENST00000556394.1:c.131G=
ENST00000556446.1:n.377G=
ENST00000602717.5:c.291G= ENSP00000487704.1:p.Leu97=
NM_013382.5:c.2076G= , LRG_844t1:c.2076G= NP_037514.2:p.Leu692=
XM_011536675.1:c.2265G= XP_011534977.1:p.Leu755=
XM_011536676.1:c.1932G= XP_011534978.1:p.Leu644=
XM_011536677.1:c.1806G= XP_011534979.1:p.Leu602=
XM_011536679.1:c.1359G= XP_011534981.1:p.Leu453=
XR_943416.1:n.2329G=
XM_011536675.2:c.2265G= XP_011534977.1:p.Leu755=
XM_011536676.2:c.1932G= XP_011534978.1:p.Leu644=
XM_011536677.3:c.1806G= XP_011534979.1:p.Leu602=
XR_001750279.1:n.2362G=
XR_001750282.1:n.3015G=
XR_943416.3:n.2327G=
NM_013382.6:c.2076G= NP_037514.2:p.Leu692=
NM_013382.7:c.2076G= MANE Select NP_037514.2:p.Leu692=