Canonical Allele Identifier: CA2148315817
Gene: POMT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77279010G= , CM000676.2:g.77279010G= GRCh38
NC_000014.8:g.77745353G= , CM000676.1:g.77745353G= GRCh37
NC_000014.7:g.76815106G= NCBI36
NG_008897.1:g.46873C= , LRG_844:g.46873C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555134.2:n.817-141C=
ENST00000556394.2:c.1433-141C= ENSP00000451967.2:n.1433-141C=
ENST00000682128.1:c.193-141C= ENSP00000506976.1:n.193-141C=
ENST00000682247.1:c.1892-152C= ENSP00000507213.1:n.1892-152C=
ENST00000682395.1:n.2356-141C=
ENST00000682459.1:n.1595-141C=
ENST00000682467.1:c.1892-502C= ENSP00000508062.1:n.1892-502C=
ENST00000682615.1:n.246-141C=
ENST00000682795.1:c.2039-141C= ENSP00000507574.1:n.2039-141C=
ENST00000682895.1:n.1608-141C=
ENST00000682955.1:n.1466-141C=
ENST00000683095.1:c.298-141C= ENSP00000508040.1:n.298-141C=
ENST00000683188.1:c.2153-141C=
ENST00000683380.1:n.1556-141C=
ENST00000683828.1:c.1601-141C=
ENST00000683907.1:c.157-141C= ENSP00000507754.1:n.157-141C=
ENST00000684172.1:c.268-141C= ENSP00000508391.1:n.268-141C=
ENST00000684259.1:n.3518C=
ENST00000684538.1:n.1130C=
ENST00000684549.1:n.1443-141C=
ENST00000261534.9:c.1892-141C= MANE Select ENSP00000261534.4:n.1892-141C=
ENST00000261534.8:c.1892-141C= ENSP00000261534.4:n.1892-141C=
ENST00000452340.7:n.2727C=
ENST00000554767.5:n.2678-141C=
ENST00000555134.1:n.817-141C=
ENST00000555710.1:c.161-49C= ENSP00000451730.1:n.161-49C=
ENST00000556171.1:c.484-141C=
ENST00000556394.1:c.88-502C=
ENST00000556446.1:n.52C=
ENST00000602717.5:c.107-141C= ENSP00000487704.1:n.107-141C=
NM_013382.5:c.1892-141C= , LRG_844t1:c.1892-141C= NP_037514.2:n.1892-141C=
XM_011536675.1:c.2081-141C= XP_011534977.1:n.2081-141C=
XM_011536676.1:c.1748-141C= XP_011534978.1:n.1748-141C=
XM_011536677.1:c.1622-141C= XP_011534979.1:n.1622-141C=
XM_011536678.1:c.*488C= XP_011534980.1:n.*488C=
XM_011536679.1:c.1175-141C= XP_011534981.1:n.1175-141C=
XR_943416.1:n.2145-141C=
XM_011536675.2:c.2081-141C= XP_011534977.1:n.2081-141C=
XM_011536676.2:c.1748-141C= XP_011534978.1:n.1748-141C=
XM_011536677.3:c.1622-141C= XP_011534979.1:n.1622-141C=
XR_001750279.1:n.2178-141C=
XR_001750282.1:n.2831-141C=
XR_943416.3:n.2143-141C=
NM_013382.6:c.1892-141C= NP_037514.2:n.1892-141C=
NM_013382.7:c.1892-141C= MANE Select NP_037514.2:n.1892-141C=