Canonical Allele Identifier: CA2148327611
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278729C= , CM000676.2:g.77278729C= GRCh38
NC_000014.8:g.77745072C= , CM000676.1:g.77745072C= GRCh37
NC_000014.7:g.76814825C= NCBI36
NG_008897.1:g.47154G= , LRG_844:g.47154G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.957G=
ENST00000556394.2:c.1573G= ENSP00000451967.2:p.Gly525=
ENST00000682128.1:c.333G= ENSP00000506976.1:n.333G=
ENST00000682247.1:c.2021G= ENSP00000507213.1:p.Arg674=
ENST00000682395.1:n.2496G=
ENST00000682459.1:n.1735G=
ENST00000682467.1:c.1892-221G= ENSP00000508062.1:n.1892-221G=
ENST00000682615.1:n.386G=
ENST00000682795.1:c.2179G= ENSP00000507574.1:p.Gly727=
ENST00000682895.1:n.1748G=
ENST00000682955.1:n.1606G=
ENST00000683095.1:c.438G= ENSP00000508040.1:n.438G=
ENST00000683188.1:c.2293G=
ENST00000683380.1:n.1696G=
ENST00000683907.1:c.297G= ENSP00000507754.1:n.297G=
ENST00000684172.1:c.408G= ENSP00000508391.1:n.408G=
ENST00000684259.1:n.3799G=
ENST00000684538.1:n.1411G=
ENST00000684549.1:n.1583G=
ENST00000261534.9:c.2032G= MANE Select ENSP00000261534.4:p.Gly678=
ENST00000261534.8:c.2032G= ENSP00000261534.4:p.Gly678=
ENST00000452340.7:n.3008G=
ENST00000554767.5:n.2818G=
ENST00000555710.1:c.393G= ENSP00000451730.1:n.393G=
ENST00000556394.1:c.88-221G=
ENST00000556446.1:n.333G=
ENST00000602717.5:c.247G= ENSP00000487704.1:p.Gly83=
NM_013382.5:c.2032G= , LRG_844t1:c.2032G= NP_037514.2:p.Gly678=
XM_011536675.1:c.2221G= XP_011534977.1:p.Gly741=
XM_011536676.1:c.1888G= XP_011534978.1:p.Gly630=
XM_011536677.1:c.1762G= XP_011534979.1:p.Gly588=
XM_011536679.1:c.1315G= XP_011534981.1:p.Gly439=
XR_943416.1:n.2285G=
XM_011536675.2:c.2221G= XP_011534977.1:p.Gly741=
XM_011536676.2:c.1888G= XP_011534978.1:p.Gly630=
XM_011536677.3:c.1762G= XP_011534979.1:p.Gly588=
XR_001750279.1:n.2318G=
XR_001750282.1:n.2971G=
XR_943416.3:n.2283G=
NM_013382.6:c.2032G= NP_037514.2:p.Gly678=
NM_013382.7:c.2032G= MANE Select NP_037514.2:p.Gly678=