Canonical Allele Identifier: CA2625846234
Gene: POMT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77279056del , CM000676.2:g.77279056del GRCh38
NC_000014.8:g.77745399del , CM000676.1:g.77745399del GRCh37
NC_000014.7:g.76815152del NCBI36
NG_008897.1:g.46829del , LRG_844:g.46829del

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.817-185del
ENST00000556394.2:c.1433-185del ENSP00000451967.2:n.1433-185del
ENST00000682128.1:c.193-185del ENSP00000506976.1:n.193-185del
ENST00000682247.1:c.1892-196del ENSP00000507213.1:n.1892-196del
ENST00000682395.1:n.2356-185del
ENST00000682459.1:n.1595-185del
ENST00000682467.1:c.1892-546del ENSP00000508062.1:n.1892-546del
ENST00000682615.1:n.246-185del
ENST00000682795.1:c.2039-185del ENSP00000507574.1:n.2039-185del
ENST00000682895.1:n.1608-185del
ENST00000682955.1:n.1466-185del
ENST00000683095.1:c.298-185del ENSP00000508040.1:n.298-185del
ENST00000683188.1:c.2153-185del
ENST00000683380.1:n.1556-185del
ENST00000683828.1:c.1601-185del
ENST00000683907.1:c.157-185del ENSP00000507754.1:n.157-185del
ENST00000684172.1:c.268-185del ENSP00000508391.1:n.268-185del
ENST00000684259.1:n.3474del
ENST00000684538.1:n.1086del
ENST00000684549.1:n.1443-185del
ENST00000261534.9:c.1892-185del MANE Select ENSP00000261534.4:n.1892-185del
ENST00000261534.8:c.1892-185del ENSP00000261534.4:n.1892-185del
ENST00000452340.7:n.2683del
ENST00000554767.5:n.2678-185del
ENST00000555134.1:n.817-185del
ENST00000555710.1:c.161-93del ENSP00000451730.1:n.161-93del
ENST00000556171.1:c.484-185del
ENST00000556394.1:c.88-546del
ENST00000556446.1:n.8del
ENST00000602717.5:c.107-185del ENSP00000487704.1:n.107-185del
NM_013382.5:c.1892-185del , LRG_844t1:c.1892-185del NP_037514.2:n.1892-185del
XM_011536675.1:c.2081-185del XP_011534977.1:n.2081-185del
XM_011536676.1:c.1748-185del XP_011534978.1:n.1748-185del
XM_011536677.1:c.1622-185del XP_011534979.1:n.1622-185del
XM_011536678.1:c.*444del XP_011534980.1:n.*444del
XM_011536679.1:c.1175-185del XP_011534981.1:n.1175-185del
XR_943416.1:n.2145-185del
XM_011536675.2:c.2081-185del XP_011534977.1:n.2081-185del
XM_011536676.2:c.1748-185del XP_011534978.1:n.1748-185del
XM_011536677.3:c.1622-185del XP_011534979.1:n.1622-185del
XR_001750279.1:n.2178-185del
XR_001750282.1:n.2831-185del
XR_943416.3:n.2143-185del
NM_013382.6:c.1892-185del NP_037514.2:n.1892-185del
NM_013382.7:c.1892-185del MANE Select NP_037514.2:n.1892-185del