Canonical Allele Identifier: CA2148327481
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278463G= , CM000676.2:g.77278463G= GRCh38
NC_000014.8:g.77744806G= , CM000676.1:g.77744806G= GRCh37
NC_000014.7:g.76814559G= NCBI36
NG_008897.1:g.47420C= , LRG_844:g.47420C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.1003C=
ENST00000556394.2:c.1619C= ENSP00000451967.2:p.Ala540=
ENST00000682247.1:c.2067C= ENSP00000507213.1:p.Gly689=
ENST00000682395.1:n.2542C=
ENST00000682459.1:n.1781C=
ENST00000682467.1:c.1937C= ENSP00000508062.1:p.Ala646=
ENST00000682795.1:c.2225C= ENSP00000507574.1:p.Ala742=
ENST00000682895.1:n.1794C=
ENST00000682955.1:n.1652C=
ENST00000683188.1:c.2339C=
ENST00000683380.1:n.1742C=
ENST00000683907.1:c.343C= ENSP00000507754.1:n.343C=
ENST00000684259.1:n.3845C=
ENST00000684538.1:n.1457C=
ENST00000684549.1:n.1629C=
ENST00000261534.9:c.2078C= MANE Select ENSP00000261534.4:p.Ala693=
ENST00000261534.8:c.2078C= ENSP00000261534.4:p.Ala693=
ENST00000452340.7:n.3054C=
ENST00000554767.5:n.2864C=
ENST00000555710.1:c.439C= ENSP00000451730.1:n.439C=
ENST00000556394.1:c.133C=
ENST00000556446.1:n.379C=
ENST00000602717.5:c.293C= ENSP00000487704.1:p.Ala98=
NM_013382.5:c.2078C= , LRG_844t1:c.2078C= NP_037514.2:p.Ala693=
XM_011536675.1:c.2267C= XP_011534977.1:p.Ala756=
XM_011536676.1:c.1934C= XP_011534978.1:p.Ala645=
XM_011536677.1:c.1808C= XP_011534979.1:p.Ala603=
XM_011536679.1:c.1361C= XP_011534981.1:p.Ala454=
XR_943416.1:n.2331C=
XM_011536675.2:c.2267C= XP_011534977.1:p.Ala756=
XM_011536676.2:c.1934C= XP_011534978.1:p.Ala645=
XM_011536677.3:c.1808C= XP_011534979.1:p.Ala603=
XR_001750279.1:n.2364C=
XR_001750282.1:n.3017C=
XR_943416.3:n.2329C=
NM_013382.6:c.2078C= NP_037514.2:p.Ala693=
NM_013382.7:c.2078C= MANE Select NP_037514.2:p.Ala693=