Canonical Allele Identifier: CA2148327485
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278469C= , CM000676.2:g.77278469C= GRCh38
NC_000014.8:g.77744812C= , CM000676.1:g.77744812C= GRCh37
NC_000014.7:g.76814565C= NCBI36
NG_008897.1:g.47414G= , LRG_844:g.47414G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.997G=
ENST00000556394.2:c.1613G= ENSP00000451967.2:p.Gly538=
ENST00000682247.1:c.2061G= ENSP00000507213.1:p.Gly687=
ENST00000682395.1:n.2536G=
ENST00000682459.1:n.1775G=
ENST00000682467.1:c.1931G= ENSP00000508062.1:p.Gly644=
ENST00000682795.1:c.2219G= ENSP00000507574.1:p.Gly740=
ENST00000682895.1:n.1788G=
ENST00000682955.1:n.1646G=
ENST00000683188.1:c.2333G=
ENST00000683380.1:n.1736G=
ENST00000683907.1:c.337G= ENSP00000507754.1:n.337G=
ENST00000684259.1:n.3839G=
ENST00000684538.1:n.1451G=
ENST00000684549.1:n.1623G=
ENST00000261534.9:c.2072G= MANE Select ENSP00000261534.4:p.Gly691=
ENST00000261534.8:c.2072G= ENSP00000261534.4:p.Gly691=
ENST00000452340.7:n.3048G=
ENST00000554767.5:n.2858G=
ENST00000555710.1:c.433G= ENSP00000451730.1:n.433G=
ENST00000556394.1:c.127G=
ENST00000556446.1:n.373G=
ENST00000602717.5:c.287G= ENSP00000487704.1:p.Gly96=
NM_013382.5:c.2072G= , LRG_844t1:c.2072G= NP_037514.2:p.Gly691=
XM_011536675.1:c.2261G= XP_011534977.1:p.Gly754=
XM_011536676.1:c.1928G= XP_011534978.1:p.Gly643=
XM_011536677.1:c.1802G= XP_011534979.1:p.Gly601=
XM_011536679.1:c.1355G= XP_011534981.1:p.Gly452=
XR_943416.1:n.2325G=
XM_011536675.2:c.2261G= XP_011534977.1:p.Gly754=
XM_011536676.2:c.1928G= XP_011534978.1:p.Gly643=
XM_011536677.3:c.1802G= XP_011534979.1:p.Gly601=
XR_001750279.1:n.2358G=
XR_001750282.1:n.3011G=
XR_943416.3:n.2323G=
NM_013382.6:c.2072G= NP_037514.2:p.Gly691=
NM_013382.7:c.2072G= MANE Select NP_037514.2:p.Gly691=