Canonical Allele Identifier: CA2148315954
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77279163C= , CM000676.2:g.77279163C= GRCh38
NC_000014.8:g.77745506C= , CM000676.1:g.77745506C= GRCh37
NC_000014.7:g.76815259C= NCBI36
NG_008897.1:g.46720G= , LRG_844:g.46720G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.817-294G=
ENST00000556394.2:c.1433-294G= ENSP00000451967.2:n.1433-294G=
ENST00000682128.1:c.193-294G= ENSP00000506976.1:n.193-294G=
ENST00000682247.1:c.1892-305G= ENSP00000507213.1:n.1892-305G=
ENST00000682395.1:n.2356-294G=
ENST00000682459.1:n.1595-294G=
ENST00000682467.1:c.1892-655G= ENSP00000508062.1:n.1892-655G=
ENST00000682615.1:n.246-294G=
ENST00000682795.1:c.2039-294G= ENSP00000507574.1:n.2039-294G=
ENST00000682895.1:n.1608-294G=
ENST00000682955.1:n.1466-294G=
ENST00000683095.1:c.298-294G= ENSP00000508040.1:n.298-294G=
ENST00000683188.1:c.2153-294G=
ENST00000683380.1:n.1556-294G=
ENST00000683828.1:c.1601-294G=
ENST00000683907.1:c.157-294G= ENSP00000507754.1:n.157-294G=
ENST00000684172.1:c.268-294G= ENSP00000508391.1:n.268-294G=
ENST00000684259.1:n.3365G=
ENST00000684538.1:n.977G=
ENST00000684549.1:n.1443-294G=
ENST00000261534.9:c.1892-294G= MANE Select ENSP00000261534.4:n.1892-294G=
ENST00000261534.8:c.1892-294G= ENSP00000261534.4:n.1892-294G=
ENST00000452340.7:n.2574G=
ENST00000554767.5:n.2678-294G=
ENST00000555134.1:n.817-294G=
ENST00000555710.1:c.161-202G= ENSP00000451730.1:n.161-202G=
ENST00000556171.1:c.484-294G=
ENST00000556394.1:c.88-655G=
ENST00000602717.5:c.107-294G= ENSP00000487704.1:n.107-294G=
NM_013382.5:c.1892-294G= , LRG_844t1:c.1892-294G= NP_037514.2:n.1892-294G=
XM_011536675.1:c.2081-294G= XP_011534977.1:n.2081-294G=
XM_011536676.1:c.1748-294G= XP_011534978.1:n.1748-294G=
XM_011536677.1:c.1622-294G= XP_011534979.1:n.1622-294G=
XM_011536678.1:c.*335G= XP_011534980.1:n.*335G=
XM_011536679.1:c.1175-294G= XP_011534981.1:n.1175-294G=
XR_943416.1:n.2145-294G=
XM_011536675.2:c.2081-294G= XP_011534977.1:n.2081-294G=
XM_011536676.2:c.1748-294G= XP_011534978.1:n.1748-294G=
XM_011536677.3:c.1622-294G= XP_011534979.1:n.1622-294G=
XR_001750279.1:n.2178-294G=
XR_001750282.1:n.2831-294G=
XR_943416.3:n.2143-294G=
NM_013382.6:c.1892-294G= NP_037514.2:n.1892-294G=
NM_013382.7:c.1892-294G= MANE Select NP_037514.2:n.1892-294G=