Canonical Allele Identifier: CA2148315905
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77279091A= , CM000676.2:g.77279091A= GRCh38
NC_000014.8:g.77745434A= , CM000676.1:g.77745434A= GRCh37
NC_000014.7:g.76815187A= NCBI36
NG_008897.1:g.46792T= , LRG_844:g.46792T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.817-222T=
ENST00000556394.2:c.1433-222T= ENSP00000451967.2:n.1433-222T=
ENST00000682128.1:c.193-222T= ENSP00000506976.1:n.193-222T=
ENST00000682247.1:c.1892-233T= ENSP00000507213.1:n.1892-233T=
ENST00000682395.1:n.2356-222T=
ENST00000682459.1:n.1595-222T=
ENST00000682467.1:c.1892-583T= ENSP00000508062.1:n.1892-583T=
ENST00000682615.1:n.246-222T=
ENST00000682795.1:c.2039-222T= ENSP00000507574.1:n.2039-222T=
ENST00000682895.1:n.1608-222T=
ENST00000682955.1:n.1466-222T=
ENST00000683095.1:c.298-222T= ENSP00000508040.1:n.298-222T=
ENST00000683188.1:c.2153-222T=
ENST00000683380.1:n.1556-222T=
ENST00000683828.1:c.1601-222T=
ENST00000683907.1:c.157-222T= ENSP00000507754.1:n.157-222T=
ENST00000684172.1:c.268-222T= ENSP00000508391.1:n.268-222T=
ENST00000684259.1:n.3437T=
ENST00000684538.1:n.1049T=
ENST00000684549.1:n.1443-222T=
ENST00000261534.9:c.1892-222T= MANE Select ENSP00000261534.4:n.1892-222T=
ENST00000261534.8:c.1892-222T= ENSP00000261534.4:n.1892-222T=
ENST00000452340.7:n.2646T=
ENST00000554767.5:n.2678-222T=
ENST00000555134.1:n.817-222T=
ENST00000555710.1:c.161-130T= ENSP00000451730.1:n.161-130T=
ENST00000556171.1:c.484-222T=
ENST00000556394.1:c.88-583T=
ENST00000602717.5:c.107-222T= ENSP00000487704.1:n.107-222T=
NM_013382.5:c.1892-222T= , LRG_844t1:c.1892-222T= NP_037514.2:n.1892-222T=
XM_011536675.1:c.2081-222T= XP_011534977.1:n.2081-222T=
XM_011536676.1:c.1748-222T= XP_011534978.1:n.1748-222T=
XM_011536677.1:c.1622-222T= XP_011534979.1:n.1622-222T=
XM_011536678.1:c.*407T= XP_011534980.1:n.*407T=
XM_011536679.1:c.1175-222T= XP_011534981.1:n.1175-222T=
XR_943416.1:n.2145-222T=
XM_011536675.2:c.2081-222T= XP_011534977.1:n.2081-222T=
XM_011536676.2:c.1748-222T= XP_011534978.1:n.1748-222T=
XM_011536677.3:c.1622-222T= XP_011534979.1:n.1622-222T=
XR_001750279.1:n.2178-222T=
XR_001750282.1:n.2831-222T=
XR_943416.3:n.2143-222T=
NM_013382.6:c.1892-222T= NP_037514.2:n.1892-222T=
NM_013382.7:c.1892-222T= MANE Select NP_037514.2:n.1892-222T=