Canonical Allele Identifier: CA390513960
Gene: POMT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77278792T>G , CM000676.2:g.77278792T>G GRCh38
NC_000014.8:g.77745135T>G , CM000676.1:g.77745135T>G GRCh37
NC_000014.7:g.76814888T>G NCBI36
NG_008897.1:g.47091A>C , LRG_844:g.47091A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.894A>C
ENST00000556394.2:c.1510A>C ENSP00000451967.2:p.Met504Leu
ENST00000682128.1:c.270A>C ENSP00000506976.1:n.270A>C
ENST00000682247.1:c.1958A>C ENSP00000507213.1:p.Asp653Ala
ENST00000682395.1:n.2433A>C
ENST00000682459.1:n.1672A>C
ENST00000682467.1:c.1892-284A>C ENSP00000508062.1:n.1892-284A>C
ENST00000682615.1:n.323A>C
ENST00000682795.1:c.2116A>C ENSP00000507574.1:p.Met706Leu
ENST00000682895.1:n.1685A>C
ENST00000682955.1:n.1543A>C
ENST00000683095.1:c.375A>C ENSP00000508040.1:n.375A>C
ENST00000683188.1:c.2230A>C
ENST00000683380.1:n.1633A>C
ENST00000683828.1:c.1678A>C
ENST00000683907.1:c.234A>C ENSP00000507754.1:p.Ter78Cys
ENST00000684172.1:c.345A>C ENSP00000508391.1:n.345A>C
ENST00000684259.1:n.3736A>C
ENST00000684538.1:n.1348A>C
ENST00000684549.1:n.1520A>C
ENST00000261534.9:c.1969A>C MANE Select ENSP00000261534.4:p.Met657Leu
ENST00000261534.8:c.1969A>C ENSP00000261534.4:p.Met657Leu
ENST00000452340.7:n.2945A>C
ENST00000554767.5:n.2755A>C
ENST00000555710.1:c.330A>C ENSP00000451730.1:n.330A>C
ENST00000556171.1:c.561A>C
ENST00000556394.1:c.88-284A>C
ENST00000556446.1:n.270A>C
ENST00000602717.5:c.184A>C ENSP00000487704.1:p.Met62Leu
NM_013382.5:c.1969A>C , LRG_844t1:c.1969A>C NP_037514.2:p.Met657Leu
XM_011536675.1:c.2158A>C XP_011534977.1:p.Met720Leu
XM_011536676.1:c.1825A>C XP_011534978.1:p.Met609Leu
XM_011536677.1:c.1699A>C XP_011534979.1:p.Met567Leu
XM_011536679.1:c.1252A>C XP_011534981.1:p.Met418Leu
XR_943416.1:n.2222A>C
XM_011536675.2:c.2158A>C XP_011534977.1:p.Met720Leu
XM_011536676.2:c.1825A>C XP_011534978.1:p.Met609Leu
XM_011536677.3:c.1699A>C XP_011534979.1:p.Met567Leu
XR_001750279.1:n.2255A>C
XR_001750282.1:n.2908A>C
XR_943416.3:n.2220A>C
NM_013382.6:c.1969A>C NP_037514.2:p.Met657Leu
NM_013382.7:c.1969A>C MANE Select NP_037514.2:p.Met657Leu