Canonical Allele Identifier: CA2148327498
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278495G= , CM000676.2:g.77278495G= GRCh38
NC_000014.8:g.77744838G= , CM000676.1:g.77744838G= GRCh37
NC_000014.7:g.76814591G= NCBI36
NG_008897.1:g.47388C= , LRG_844:g.47388C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.971C=
ENST00000556394.2:c.1587C= ENSP00000451967.2:p.Asp529=
ENST00000682247.1:c.2035C= ENSP00000507213.1:p.His679=
ENST00000682395.1:n.2510C=
ENST00000682459.1:n.1749C=
ENST00000682467.1:c.1905C= ENSP00000508062.1:p.Asp635=
ENST00000682795.1:c.2193C= ENSP00000507574.1:p.Asp731=
ENST00000682895.1:n.1762C=
ENST00000682955.1:n.1620C=
ENST00000683188.1:c.2307C=
ENST00000683380.1:n.1710C=
ENST00000683907.1:c.311C= ENSP00000507754.1:n.311C=
ENST00000684259.1:n.3813C=
ENST00000684538.1:n.1425C=
ENST00000684549.1:n.1597C=
ENST00000261534.9:c.2046C= MANE Select ENSP00000261534.4:p.Asp682=
ENST00000261534.8:c.2046C= ENSP00000261534.4:p.Asp682=
ENST00000452340.7:n.3022C=
ENST00000554767.5:n.2832C=
ENST00000555710.1:c.407C= ENSP00000451730.1:n.407C=
ENST00000556394.1:c.101C=
ENST00000556446.1:n.347C=
ENST00000602717.5:c.261C= ENSP00000487704.1:p.Asp87=
NM_013382.5:c.2046C= , LRG_844t1:c.2046C= NP_037514.2:p.Asp682=
XM_011536675.1:c.2235C= XP_011534977.1:p.Asp745=
XM_011536676.1:c.1902C= XP_011534978.1:p.Asp634=
XM_011536677.1:c.1776C= XP_011534979.1:p.Asp592=
XM_011536679.1:c.1329C= XP_011534981.1:p.Asp443=
XR_943416.1:n.2299C=
XM_011536675.2:c.2235C= XP_011534977.1:p.Asp745=
XM_011536676.2:c.1902C= XP_011534978.1:p.Asp634=
XM_011536677.3:c.1776C= XP_011534979.1:p.Asp592=
XR_001750279.1:n.2332C=
XR_001750282.1:n.2985C=
XR_943416.3:n.2297C=
NM_013382.6:c.2046C= NP_037514.2:p.Asp682=
NM_013382.7:c.2046C= MANE Select NP_037514.2:p.Asp682=